Page last updated: 2024-10-19

niacinamide and Acute Myelogenous Leukemia

niacinamide has been researched along with Acute Myelogenous Leukemia in 137 studies

nicotinamide : A pyridinecarboxamide that is pyridine in which the hydrogen at position 3 is replaced by a carboxamide group.

Research Excerpts

ExcerptRelevanceReference
"Twelve patients with acute leukemia (11 with acute myeloid leukemia [AML]) received sorafenib on days 1 to 7 and then concurrently with cytarabine (1 g/m(2)) and clofarabine (stratum one: 40 mg/m(2), n = 10; stratum two [recent transplantation or fungal infection]: 20 mg/m(2), n = 2) on days 8 to 12."9.15Phase I pharmacokinetic and pharmacodynamic study of the multikinase inhibitor sorafenib in combination with clofarabine and cytarabine in pediatric relapsed/refractory leukemia. ( Baker, SD; Campana, D; Christensen, R; Coustan-Smith, E; Furmanski, BD; Heym, KM; Inaba, H; Li, L; Mascara, GP; Onciu, M; Pounds, SB; Pui, CH; Ribeiro, RC; Rubnitz, JE; Shurtleff, SA, 2011)
"Sorafenib was 1000- to 3000-fold more effective in inducing growth arrest and apoptosis in Ba/F3 cells with FLT3-ITD or D835G mutations than in Ba/F3 cells with FLT3-D835Y mutant or wild-type FLT3 and inhibited the phosphorylation of tyrosine residues in ITD mutant but not wild-type FLT3 protein."6.73Mutant FLT3: a direct target of sorafenib in acute myelogenous leukemia. ( Andreeff, M; Cortes, J; Estrov, Z; Harris, D; Konopleva, M; Ling, X; McQueen, T; Quintás-Cardama, A; Shi, YX; Small, D; Zhang, W, 2008)
"The prognosis for children with acute myelogenous leukemia (AML) has improved with overall survival rates of up to 65% [Pui et al."5.38Sorafenib as treatment for relapsed or refractory pediatric acute myelogenous leukemia. ( Cooper, T; Watt, TC, 2012)
"Twelve patients with acute leukemia (11 with acute myeloid leukemia [AML]) received sorafenib on days 1 to 7 and then concurrently with cytarabine (1 g/m(2)) and clofarabine (stratum one: 40 mg/m(2), n = 10; stratum two [recent transplantation or fungal infection]: 20 mg/m(2), n = 2) on days 8 to 12."5.15Phase I pharmacokinetic and pharmacodynamic study of the multikinase inhibitor sorafenib in combination with clofarabine and cytarabine in pediatric relapsed/refractory leukemia. ( Baker, SD; Campana, D; Christensen, R; Coustan-Smith, E; Furmanski, BD; Heym, KM; Inaba, H; Li, L; Mascara, GP; Onciu, M; Pounds, SB; Pui, CH; Ribeiro, RC; Rubnitz, JE; Shurtleff, SA, 2011)
" In conclusion, sorafenib is active and well tolerated in acute myelogenous leukemia with fms-like tyrosine kinase 3 internal tandem duplication mutation."5.15Phase I study of sorafenib in patients with refractory or relapsed acute leukemias. ( Andreeff, M; Borthakur, G; Cortes, JE; Faderl, S; Kantarjian, H; Konopleva, M; Mathews, S; Ravandi, F; Verstovsek, S; Wright, JJ; Zhang, W, 2011)
"A 10-year-old boy with FLT3-ITD-positive acute myelogenous leukemia who developed PRES during sorafenib treatment has been presented here."3.83Sorafenib-induced Posterior Reversible Encephalopathy Syndrome in a Child With FLT3-ITD-positive Acute Myeloid Leukemia. ( Bayhan, T; Cetin, M; Gumruk, F; Isgandarova, F; Kuskonmaz, B; Tavil, B; Unal, S, 2016)
"To evaluate the clinical activity of sequential therapy with sorafenib and sunitinib in FMS-like tyrosine kinase 3 (FLT3)-internal tandem duplication (ITD)-positive acute myelogenous leukemia (AML) and monitor the emergence of secondary FLT3 tyrosine kinase domain (TKD) mutations during treatment."3.79Emergence of polyclonal FLT3 tyrosine kinase domain mutations during sequential therapy with sorafenib and sunitinib in FLT3-ITD-positive acute myeloid leukemia. ( Baker, SD; Buaboonnam, J; Enemark, EJ; Inaba, H; Mullighan, CG; Neale, GA; Olsen, SR; Orwick, S; Rubnitz, JE; Shurtleff, S; Wang, YD; Zatechka, DS; Zimmerman, EI, 2013)
"We compared the antitumor activities of the multitargeted tyrosine kinase inhibitors imatinib, sorafenib, and sunitinib to determine which inhibitor is best suited to be used for the treatment of acute myelogenous leukemia (AML)."3.74Comparison of antitumor effects of multitargeted tyrosine kinase inhibitors in acute myelogenous leukemia. ( Baker, SD; Dahl, GV; Hu, S; Inaba, H; Minkin, P; Niu, H; Orwick, S; Rubnitz, J; Shimada, A, 2008)
"Patients with acute myeloid leukemia (AML) carrying FLT3-ITD mutations (FLT3-ITD+) who relapse after allogeneic transplantation (allo-SCT) have a very dismal prognosis with the currently available treatment options."2.84Sorafenib and azacitidine as salvage therapy for relapse of FLT3-ITD mutated AML after allo-SCT. ( Dienst, A; Germing, U; Haas, R; Heyn, C; Kobbe, G; Kondakci, M; Nachtkamp, K; Rautenberg, C; Schmidt, PV; Schroeder, T, 2017)
"Sorafenib was initiated between days 45 and 120 after HSCT and continued for 12 28-day cycles."2.79Phase I trial of maintenance sorafenib after allogeneic hematopoietic stem cell transplantation for fms-like tyrosine kinase 3 internal tandem duplication acute myeloid leukemia. ( Antin, JH; Ballen, K; Chen, YB; Connolly, C; Curtis, M; Cutler, C; Del Rio, C; Dey, BR; El-Jawahri, A; Fathi, AT; Ho, VT; Joyce, A; Lane, AA; Levis, M; Li, S; McAfee, S; Rajkhowa, T; Rudek, M; Soiffer, R; Spitzer, TR; Valles, B; Verselis, S, 2014)
"Forty-three acute myeloid leukemia (AML) patients with a median age of 64 years (range, 24-87 years) were enrolled; 37 were evaluable for response."2.78Phase 2 study of azacytidine plus sorafenib in patients with acute myeloid leukemia and FLT-3 internal tandem duplication mutation. ( Alattar, ML; Andreeff, M; Borthakur, G; Burger, J; Cortes, J; Daver, N; Dellasala, S; Faderl, S; Garcia-Manero, G; Grunwald, MR; Kadia, T; Kantarjian, H; Konopleva, M; Levis, M; Nazha, A; Pierce, S; Rajkhowa, T; Ravandi, F; Richie, MA; Rudek, MA, 2013)
"The prognosis of elderly patients with acute myeloid leukemia (AML) is still dismal even with intensive chemotherapy."2.78Sorafenib in combination with intensive chemotherapy in elderly patients with acute myeloid leukemia: results from a randomized, placebo-controlled trial. ( Aulitzky, W; Berdel, WE; Blau, I; Brandts, C; Brunnberg, U; Duyster, J; Ehninger, G; Fischer, T; Giagounidis, A; Heinecke, A; Krämer, A; Kreuzer, KA; Krug, U; Kunzmann, V; Müller-Tidow, C; Neubauer, A; Noppeney, R; Ottmann, O; Reichle, A; Sauerland, MC; Schaich, M; Serve, H; Steffen, B; Stuhlmann, R; Thiede, C; Wagner, R; Wandt, H, 2013)
"Sorafenib is active in patients with acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS)."2.78A phase I/II study of sorafenib in combination with low dose cytarabine in elderly patients with acute myeloid leukemia or high-risk myelodysplastic syndrome from the National Cancer Institute of Canada Clinical Trials Group: trial IND.186. ( Assouline, SE; Brandwein, J; Caplan, S; Couban, S; Eisenhauer, EA; Foo, A; Kamel-Reid, S; Leber, B; Macdonald, DA; Walsh, W, 2013)
"The sorafenib response was lost in most patients after 72 (range 54-287) days but the FLT3 and downstream effectors remained suppressed."2.77Sorafenib treatment of FLT3-ITD(+) acute myeloid leukemia: favorable initial outcome and mechanisms of subsequent nonresponsiveness associated with the emergence of a D835 mutation. ( Cheung, AM; Choi, WW; Chow, HC; Eaves, C; Fung, TK; Han, HH; Ho, C; Kwong, YL; Leung, AY; Lok, S; Ma, AC; Man, CH, 2012)
"Our data demonstrate that acute myeloid leukemia cells show a variable but overall good susceptibility to the innovative therapeutic combination of sorafenib+nutlin-3, which differentially involves the pro-apoptotic Bcl-2 family members Bax and Bak in p53(wild-type) and p53(deleted) cells."2.77The sorafenib plus nutlin-3 combination promotes synergistic cytotoxicity in acute myeloid leukemic cells irrespectively of FLT3 and p53 status. ( Celeghini, C; di Iasio, MG; Lanza, F; Melloni, E; Ongari, M; Secchiero, P; Tiribelli, M; Voltan, R; Zauli, G, 2012)
"Sorafenib was 1000- to 3000-fold more effective in inducing growth arrest and apoptosis in Ba/F3 cells with FLT3-ITD or D835G mutations than in Ba/F3 cells with FLT3-D835Y mutant or wild-type FLT3 and inhibited the phosphorylation of tyrosine residues in ITD mutant but not wild-type FLT3 protein."2.73Mutant FLT3: a direct target of sorafenib in acute myelogenous leukemia. ( Andreeff, M; Cortes, J; Estrov, Z; Harris, D; Konopleva, M; Ling, X; McQueen, T; Quintás-Cardama, A; Shi, YX; Small, D; Zhang, W, 2008)
"We previously reported a flow cytometry technique to monitor pharmacodynamic effects of the raf kinase inhibitor BAY 43-9006 based on the ability of phorbol ester (PMA) to phosphorylate extracellular-regulated kinase (ERK) in peripheral blood (Chow et al."2.72Pharmacodynamic monitoring of BAY 43-9006 (Sorafenib) in phase I clinical trials involving solid tumor and AML/MDS patients, using flow cytometry to monitor activation of the ERK pathway in peripheral blood cells. ( Chow, S; Hedley, D; Tong, FK, 2006)
"Although both reached severe aplasia of the bone marrow without blastic infiltration, death occurred with neutropenic sepsis."2.52Hypertension and Life-Threatening Bleeding in Children with Relapsed Acute Myeloblastic Leukemia Treated with FLT3 Inhibitors. ( Aydınok, Y; Balkan, C; Karadaş, N; Kavaklı, K; Önder Siviş, Z; Yılmaz Karapınar, D, 2015)
"Sorafenib is used for the treatment of acute myeloid leukemia patients carrying internal tandem duplication of fms-like tyrosine kinase 3 (FLT3-ITD) mutation."2.52A minireview on NHE1 inhibitors. A rediscovered hope in oncohematology. ( Mihaila, RG, 2015)
"Survival of patients with acute myelogenous leukemia (AML), particularly in younger patients, has improved in recent years due to improved understanding of disease biology, post remission therapies and supportive care."2.50Allogeneic stem cell transplantation and targeted therapy for FLT3/ITD+ acute myeloid leukemia: an update. ( Hu, B; Mohty, M; Savani, BN; Vikas, P, 2014)
"Treatment of acute myeloid leukemia remains a therapeutic challenge."2.49Rapid induction of complete molecular remission by sequential therapy with LDAC and sorafenib in FLT3-ITD-positive patients unfit for intensive treatment: two cases and review of the literature. ( Fischer, T; Heidel, FH; Jentsch-Ullrich, K; Krogel, C; Luehr, H; Schalk, E; Schnoeder, TM; Wolleschak, D, 2013)
"The treatment of acute myeloid leukemia has not changed significantly over the last 40 years."2.48Molecular targeted therapy in acute myeloid leukemia. ( Cortes, J; Daver, N, 2012)
" In this article, we describe the application of flow cytometry to the pharmacodynamic monitoring of molecular-targeted agents in leukemia patients."2.44Pharmacodynamic monitoring of molecular-targeted agents in the peripheral blood of leukemia patients using flow cytometry. ( Chow, S; Goolsby, C; Hedley, DW; Shankey, TV, 2008)
"5) after allogeneic HSCT with a median daily dosage of 400 mg (range: 200-800) orally, and lasted a median of 11."1.72Sorafenib maintenance after hematopoietic stem cell transplantation improves outcome of FLT3-ITD-mutated acute myeloid leukemia. ( Aydin, S; Brunello, L; Busca, A; Cattel, F; Dellacasa, CM; Dogliotti, I; Giaccone, L; Passera, R; Poggiu, M; Scaldaferri, M; Zallio, F, 2022)
"Sorafenib dosing was individualized, starting at 200 mg twice a day (BID), and titrated based on tolerability or toxicities until a tolerable dose was identified."1.56A Prospective Study of Peritransplant Sorafenib for Patients with FLT3-ITD Acute Myeloid Leukemia Undergoing Allogeneic Transplantation. ( Baer, MR; Dezern, A; Duong, VH; Emadi, A; Gocke, C; Gojo, I; Greer, J; Jones, RJ; Karp, J; Levis, M; Pratz, KW; Rosner, G; Rudek, MA; Smith, BD; Wright, JJ; Zahurak, M, 2020)
"We studied three FLT3 ITD acute myeloid leukemia (AML) patients who relapsed after allogeneic haematopoietic stem cell transplantation (alloHSCT) and received multikinase inhibitor (MKI) sorafenib as part of salvage therapy."1.48The sorafenib anti-relapse effect after alloHSCT is associated with heightened alloreactivity and accumulation of CD8+PD-1+ (CD279+) lymphocytes in marrow. ( Dworacki, G; Jaskula, E; Lange, A; Lange, J; Mordak-Domagala, M; Nowak, D; Sedzimirska, M; Simiczyjew, A, 2018)
"To explore the efficacy of sorafenib combined with chemotherapy and donor lymphocyte infusion (DLI) in patients with FLT3-positive acute myeloid leukemia (AML) relapsed after allogeneic hematopoietic stem cell transplantation (allo-HSCT)."1.48[Sorafenib combined with chemotherapy and donor lymphocyte infusion as salvage therapy in patients with FLT3-positive acute myeloid leukemia relapse after allogeneic hematopoietic stem cell transplantation]. ( Fan, ZP; Huang, F; Liu, QF; Sun, J; Wang, ZX; Xu, N; Xuan, L; Ye, JY; Zhang, Y; Zhou, X, 2018)
"Sorafenib treatment after HSCT appears to be feasible and highly effective with dose individualization according to patient tolerability."1.46Efficacy and feasibility of sorafenib as a maintenance agent after allogeneic hematopoietic stem cell transplantation for Fms-like tyrosine kinase 3-mutated acute myeloid leukemia. ( Ahmed, SO; Aljurf, M; Antar, A; Battipaglia, G; Bazarbachi, A; Belhocine, R; Brissot, E; Dulery, R; Eder, S; El Cheikh, J; Giannotti, F; Isnard, F; Jestin, M; Lapusan, S; Legrand, O; Massoud, R; Mohty, M; Rasheed, W; Rubio, MT; Ruggeri, A; Shaheen, M; Vekhoff, A, 2017)
"Sorafenib may enable cure of a proportion of very poor risk FLT3-ITD-positive AML relapsing after allo-SCT."1.46Long-term survival of sorafenib-treated FLT3-ITD-positive acute myeloid leukaemia patients relapsing after allogeneic stem cell transplantation. ( Basara, N; Burchert, A; Ditschkowski, M; Dreger, P; Fey, MF; Finck, A; Finke, J; Giagounidis, A; Götze, K; Kobbe, G; Lübbert, M; Metzelder, SK; Meyer, RG; Neubauer, A; Pabst, T; Salih, HR; Scholl, S; Schroeder, T; Wollmer, E, 2017)
"Sorafenib is a promising agent for treating pediatric refractory acute myeloid leukemia (AML) exhibiting FMS-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD); however, its optimal use needs to be established."1.46Sorafenib Therapy for Pediatric Acute Myeloid Leukemia with FMS-like Tyrosine Kinase 3-internal Tandem Duplication Mutations: 2 Case Reports. ( Hosoi, H; Imamura, T; Ishida, H; Kanayama, T; Kawashima-Goto, S; Miyachi, M; Nakatani, T; Osone, S; Sugimoto, A; Takai, A; Tamura, S; Tsuma, Y, 2017)
"To study the efficacy and safety of sorafenib combined with low dose cytarabine for treating patients with FLT3(+) relapsed and refractory acute myeloid leukemia (FLT3(+) RR-AML)."1.43[Clinical Efficacy of Sorafenib Combined with Low Dose Cytarabine for Treating Patients with FLT3+ Relapsed and Refractory Acute Myeloid Leukemia]. ( DU, QF; Huang, YX; Liu, XS; Long, H; Wu, BY; Xu, JH; Zhu, JY, 2016)
"Sorafenib was associated with improved 2-year PFS (82% vs."1.43Haematopoietic cell transplantation with and without sorafenib maintenance for patients with FLT3-ITD acute myeloid leukaemia in first complete remission. ( Alyea, EP; Antin, JH; Ballen, KK; Brunner, AM; Chen, YB; Collier, K; Connolly, C; Cutler, CS; Deangelo, DJ; Dey, BR; El-Jawahri, A; Fathi, AT; Ho, VT; Koreth, J; Li, S; McAfee, SL; Nikiforow, S; Soiffer, RJ; Spitzer, TR; Stone, RM; Wadleigh, M, 2016)
"Sorafenib treatment protocols included sorafenib in combination with chemotherapy inducing remission, and sorafenib monotherapy as mauntenance treatment after complete remission (CR)."1.43[Sorafenib as salvage therapy in refractory relapsed acute myeloid leukemia with positive FLT3 mutation]. ( Fan, Z; Gao, Y; Huang, F; Jiang, Q; Liu, Q; Sun, J; Xu, N; Xuan, L; Zhang, Y, 2016)
"FMS-like tyrosine kinase 3 (FLT3)-mutant acute myeloid leukemia (AML) portends a poor prognosis, and ineffective targeting of the leukemic stem cell (LSC) population remains one of several obstacles in treating this disease."1.43All-trans retinoic acid synergizes with FLT3 inhibition to eliminate FLT3/ITD+ leukemia stem cells in vitro and in vivo. ( Aplan, PD; Bruner, JK; Duffield, AS; Ghiaur, G; Greenblatt, SM; Jones, RJ; Jung, E; Li, L; Ma, HS; Nguyen, B; Shirley, CM; Small, D, 2016)
" In 5 patients with pronounced toxicity, we switched to an alternating dosing schedule with 1 month on/1 month off sorafenib."1.42Synergistic effect of sorafenib and cGvHD in patients with high-risk FLT3-ITD+AML allows long-term disease control after allogeneic transplantation. ( Gerull, S; Halter, JP; Heim, D; Medinger, M; Passweg, JR; Tschan-Plessl, A, 2015)
"Sorafenib was initiated at a median of 100 days post HSCT."1.42Sorafenib treatment following hematopoietic stem cell transplant in pediatric FLT3/ITD acute myeloid leukemia. ( Adlard, K; Chang, B; Cooper, T; Estey, E; Garee, A; Gross, T; Gupta, S; Ho, PA; McGoldrick, S; Meshinchi, S; Neudorf, S; Pollard, JA; Sisler, I; Tarlock, K; Templeman, T; Thomson, B; Watt, T; Woolfrey, A, 2015)
"Sorafenib is a tyrosine kinase inhibitor active against RAF, VEGF, and FLT3-ITD."1.42Sorafenib Maintenance Appears Safe and Improves Clinical Outcomes in FLT3-ITD Acute Myeloid Leukemia After Allogeneic Hematopoietic Cell Transplantation. ( Antar, A; Bazarbachi, A; Kharfan-Dabaja, MA; Mahfouz, R, 2015)
"FLT3(ITD) subtype acute myeloid leukemia (AML) has a poor prognosis with currently available therapies."1.40FLT3 and CDK4/6 inhibitors: signaling mechanisms and tumor burden in subcutaneous and orthotopic mouse models of acute myeloid leukemia. ( D'Argenio, DZ; Hsu, CP; Huard, J; Kuchimanchi, M; Lu, JF; Ma, J; Sun, YN; Weidner, M; Xu, G; Xu, Y; Zhang, Y, 2014)
"Ponatinib (AP24534) is a multikinase inhibitor with in vitro and clinical activity in tyrosine kinase inhibitor (TKI)-resistant chronic myeloid leukemia, irrespective of BCR-ABL KD mutation."1.39Activity of ponatinib against clinically-relevant AC220-resistant kinase domain mutants of FLT3-ITD. ( Damon, LE; Lasater, EA; Lin, KC; Salerno, S; Shah, NP; Smith, CC; Stewart, WK; Zhu, X, 2013)
"The prognosis for children with acute myelogenous leukemia (AML) has improved with overall survival rates of up to 65% [Pui et al."1.38Sorafenib as treatment for relapsed or refractory pediatric acute myelogenous leukemia. ( Cooper, T; Watt, TC, 2012)
"Sorafenib is a multi-kinase inhibitor with activity against several intracellular kinases which may play a role in the pathogenesis of acute myeloid leukemia (AML)."1.38Survey and analysis of the efficacy and prescription pattern of sorafenib in patients with acute myeloid leukemia. ( Berdel, WE; Brandts, C; Ehninger, G; Haibach, M; Hentrich, M; Junghanß, C; Krämer, A; Kramer, M; Krause, SW; Müller-Tidow, C; Pflüger, KH; Ritter, B; Röllig, C; Schleyer, E; Serve, H; Shaid, S, 2012)
"We examined in vivo FLT3 inhibition in acute myeloid leukemia patients treated with chemotherapy followed by the FLT3 inhibitor lestaurtinib, comparing newly diagnosed acute myeloid leukemia patients with relapsed patients."1.37FLT3 ligand impedes the efficacy of FLT3 inhibitors in vitro and in vivo. ( Burnett, A; Galkin, S; Knapper, S; Levis, M; Sato, T; Small, D; Smith, BD; White, P; Yang, X, 2011)
"Sorafenib in combination with cytarabine resulted in strong anti-AML activity in vitro and in vivo."1.37Activity of the multikinase inhibitor sorafenib in combination with cytarabine in acute myeloid leukemia. ( Baker, SD; Calabrese, C; Campana, D; Fan, Y; Hu, S; Inaba, H; Niu, H; Orwick, S; Panetta, JC; Pounds, S; Rehg, JE; Rose, C; Rubnitz, JE; Yang, S, 2011)
"Patients with acute myeloid leukemia (AML) and internal tandem duplication of FMS-like tyrosine kinase receptor-3 gene (FLT3-ITD) mutation have poor prognoses and are often treated with allogeneic hematopoietic stem cell transplantation (HSCT)."1.37Treatment of FLT3-ITD-positive acute myeloid leukemia relapsing after allogeneic stem cell transplantation with sorafenib. ( Andreeff, M; Bashir, Q; Bayraktar, UD; Champlin, RE; Chen, J; Chiattone, A; Cortes, J; de Lima, M; Giralt, S; Kantarjian, H; Kebriaei, P; Konopleva, M; McCue, D; Qazilbash, M; Ravandi, F; Sharma, M, 2011)
"Sorafenib is an orally active multikinase inhibitor with potent activity against FLT3 and the Raf/ERK/MEK kinase pathway."1.37Patterns of molecular response to and relapse after combination of sorafenib, idarubicin, and cytarabine in patients with FLT3 mutant acute myeloid leukemia. ( Abril, C; Al-Kali, A; Brandt, M; Cortes, J; Faderl, S; Jones, D; Kantarjian, H; Pierce, S; Ravandi, F, 2011)
"We report the results of a phase I dose escalation trial of the multikinase inhibitor sorafenib in relapsed and refractory acute leukemia patients using an intermittent dosing regimen."1.36A pharmacodynamic study of sorafenib in patients with relapsed and refractory acute leukemias. ( Baker, SD; Carducci, MA; Cho, E; Gore, SD; Karp, JE; Levis, MJ; McDevitt, M; Pratz, KW; Rudek, MA; Smith, BD; Stine, A; Wright, JJ; Zhao, M, 2010)
" Exposure of cells to noninducing concentrations of these compounds caused a leftward shift in the dose-response curve for RA; maturation was observed at 10(-11) M RA in the presence of either 2 mM NAm or 0."1.27Maturation of human promyelocytic leukemia cells induced by nicotinamide: evidence of a regulatory role for ADP-ribosylation of chromosomal proteins. ( Davies, PJ; Johnson, GS; Lucas, DL; Tanuma, S; Wright, DG, 1984)

Research

Studies (137)

TimeframeStudies, this research(%)All Research%
pre-19904 (2.92)18.7374
1990's0 (0.00)18.2507
2000's11 (8.03)29.6817
2010's116 (84.67)24.3611
2020's6 (4.38)2.80

Authors

AuthorsStudies
Aydin, S1
Passera, R1
Scaldaferri, M1
Dellacasa, CM1
Poggiu, M1
Cattel, F1
Zallio, F1
Brunello, L1
Giaccone, L1
Dogliotti, I1
Busca, A1
Ai, H3
Mi, RH1
Chen, L1
Ji, X1
Yin, QS1
Wei, XD1
Song, YP2
Pratz, KW6
Rudek, MA4
Smith, BD5
Karp, J1
Gojo, I1
Dezern, A1
Jones, RJ3
Greer, J1
Gocke, C1
Baer, MR1
Duong, VH1
Rosner, G1
Zahurak, M1
Wright, JJ3
Emadi, A2
Levis, M10
Jones, CL1
Stevens, BM1
Pollyea, DA1
Culp-Hill, R1
Reisz, JA1
Nemkov, T1
Gehrke, S1
Gamboni, F1
Krug, A1
Winters, A1
Pei, S1
Gustafson, A1
Ye, H1
Inguva, A1
Amaya, M1
Minhajuddin, M1
Abbott, D1
Becker, MW1
DeGregori, J1
Smith, CA1
D'Alessandro, A1
Jordan, CT2
Zhang, TY1
Majeti, R1
Damnernsawad, A1
Bottomly, D1
Kurtz, SE1
Eide, CA1
McWeeney, SK1
Tyner, JW1
Nechiporuk, T1
Battipaglia, G1
Ruggeri, A1
Massoud, R1
El Cheikh, J1
Jestin, M1
Antar, A2
Ahmed, SO1
Rasheed, W1
Shaheen, M1
Belhocine, R1
Brissot, E1
Dulery, R1
Eder, S1
Giannotti, F1
Isnard, F1
Lapusan, S1
Rubio, MT1
Vekhoff, A1
Aljurf, M1
Legrand, O1
Mohty, M2
Bazarbachi, A2
Roolf, C1
Dybowski, N1
Sekora, A1
Mueller, S1
Knuebel, G1
Tebbe, A1
Murua Escobar, H1
Godl, K1
Junghanss, C1
Schaab, C1
Bruner, JK2
Ma, HS2
Li, L4
Qin, ACR1
Levis, MJ2
Pratilas, CA1
Small, D5
Metzelder, SK5
Schroeder, T4
Lübbert, M2
Ditschkowski, M1
Götze, K2
Scholl, S4
Meyer, RG2
Dreger, P2
Basara, N2
Fey, MF1
Salih, HR2
Finck, A2
Pabst, T1
Giagounidis, A4
Kobbe, G4
Wollmer, E2
Finke, J1
Neubauer, A7
Burchert, A6
Lange, A1
Jaskula, E1
Lange, J1
Dworacki, G1
Nowak, D1
Simiczyjew, A1
Mordak-Domagala, M1
Sedzimirska, M1
Xuan, L2
Fan, ZP1
Zhang, Y5
Xu, N2
Ye, JY1
Zhou, X1
Wang, ZX1
Sun, J4
Liu, QF1
Huang, F2
Smith, CC1
Lasater, EA1
Zhu, X2
Lin, KC1
Stewart, WK1
Damon, LE1
Salerno, S1
Shah, NP1
Ravandi, F11
Alattar, ML1
Grunwald, MR1
Rajkhowa, T3
Richie, MA1
Pierce, S3
Daver, N4
Garcia-Manero, G5
Faderl, S5
Nazha, A1
Konopleva, M12
Borthakur, G8
Burger, J1
Kadia, T1
Dellasala, S1
Andreeff, M13
Cortes, J8
Kantarjian, H8
Chandran, P1
Gupta, N1
Retnakumari, AP1
Malarvizhi, GL1
Keechilat, P1
Nair, S1
Koyakutty, M1
Wolleschak, D1
Schalk, E1
Krogel, C1
Schnoeder, TM1
Luehr, H1
Jentsch-Ullrich, K1
Fischer, T2
Heidel, FH2
Serve, H3
Krug, U3
Wagner, R1
Sauerland, MC1
Heinecke, A1
Brunnberg, U1
Schaich, M2
Ottmann, O1
Duyster, J2
Wandt, H1
Reichle, A2
Aulitzky, W2
Noppeney, R2
Blau, I1
Kunzmann, V2
Stuhlmann, R2
Krämer, A3
Kreuzer, KA1
Brandts, C2
Steffen, B1
Thiede, C2
Müller-Tidow, C3
Ehninger, G4
Berdel, WE3
Baker, SD6
Zimmerman, EI2
Wang, YD1
Orwick, S4
Zatechka, DS1
Buaboonnam, J2
Neale, GA1
Olsen, SR1
Enemark, EJ1
Shurtleff, S1
Rubnitz, JE3
Mullighan, CG1
Inaba, H5
Jiang, ZH1
Feng, FE1
Lin, XQ1
Lu, J1
Johnston, DL1
Nagarajan, R1
Caparas, M1
Schulte, F1
Cullen, P1
Aplenc, R1
Sung, L1
Turner, DC1
Hu, S3
Roberts, MS1
Janke, LJ1
Ramachandran, A2
Stewart, CF1
Fontanelli, G1
Rocco, M1
Caracciolo, F1
Benedetti, E1
Buda, G1
Orciuolo, E1
Carulli, G1
Galimberti, S1
Azzarà, A1
Petrini, M1
Hu, B1
Vikas, P1
Savani, BN1
Arana Yi, C1
Cortes, JE6
Jabbour, E1
O'Brien, S2
Estrov, Z4
Thomas, D3
Brandt, M3
Pratz, K2
Luthra, R4
Keegan, K1
Li, C1
Li, Z1
Ma, J2
Ragains, M1
Coberly, S1
Hollenback, D1
Eksterowicz, J1
Liang, L1
Weidner, M2
Huard, J2
Wang, X2
Alba, G1
Orf, J1
Lo, MC1
Zhao, S1
Ngo, R1
Chen, A1
Liu, L1
Carlson, T1
Quéva, C1
McGee, LR1
Medina, J1
Kamb, A1
Wickramasinghe, D1
Dai, K1
Man, CH4
Lam, SS2
Sun, MK1
Chow, HC3
Gill, H3
Kwong, YL4
Leung, AY4
Zhang, W5
Gao, C1
Chen, Y1
Jacamo, RO1
Guenounou, S1
Delabesse, E1
Récher, C1
Alvarado, Y1
Kantarjian, HM3
Pemmaraju, N1
Sammons, SL1
Karp, JE2
Liegel, J1
Courville, E1
Sachs, Z1
Ustun, C1
Fathi, AT3
Lin, WM1
Durazzo, T1
Piris, A1
Sadrzadeh, H1
Bernardo, L1
Borger, DR1
McAfee, SL2
Kroshinsky, D1
Chen, YB3
Cummins, KD1
Jane, SM1
Ninkovic, S1
Nikovic, S1
Bazargan, A1
Filshie, R1
Sutrave, G1
Hertzberg, M1
Scott, A1
Lane, S1
Yannakou, CK1
Ritchie, D1
D'Rozario, J1
Black, J1
Bavishi, K1
Wei, A2
Song, G1
Valdez, BC1
Li, Y1
Liu, Y2
Champlin, RE2
Andersson, BS1
Li, S2
Lane, AA1
Connolly, C2
Del Rio, C1
Valles, B1
Curtis, M1
Ballen, K1
Cutler, C1
Dey, BR2
El-Jawahri, A2
Ho, VT2
Joyce, A1
McAfee, S1
Rudek, M1
Verselis, S1
Antin, JH2
Spitzer, TR2
Soiffer, R1
Hsu, CP1
Lu, JF1
Kuchimanchi, M1
Sun, YN1
Xu, G1
Xu, Y1
D'Argenio, DZ1
Galanis, A1
Kuo, YH1
Bhatia, R1
Bruedigam, C1
Bagger, FO1
Paine Kuhn, C1
Guignes, S1
Song, A1
Austin, R1
Vu, T1
Lee, E1
Riyat, S1
Moore, AS2
Lock, RB2
Bullinger, L1
Hill, GR1
Armstrong, SA1
Williams, DA1
Lane, SW1
Kharfan-Dabaja, MA1
Mahfouz, R1
Tarlock, K1
Chang, B1
Cooper, T2
Gross, T1
Gupta, S1
Neudorf, S1
Adlard, K1
Ho, PA1
McGoldrick, S1
Watt, T1
Templeman, T1
Sisler, I1
Garee, A1
Thomson, B1
Woolfrey, A1
Estey, E1
Meshinchi, S1
Pollard, JA1
Fouladi, F1
Jehn, LB1
Hub, F1
Henkenius, K1
Brendel, C2
Stiewe, T2
Ip, AH1
Choi, WW2
Liu, S1
Wei, X2
Yin, Q2
Mi, R2
Wang, P2
Zhao, H1
Han, L1
Song, Y1
Yılmaz Karapınar, D1
Karadaş, N1
Önder Siviş, Z1
Balkan, C1
Kavaklı, K1
Aydınok, Y1
Xu, H1
Giri, S1
Hamdeh, S1
Bhatt, VR1
Schwarz, JK1
Michel, C1
von Bonin, M2
Rehberger, M1
Hessmann, E1
Inselmann, S1
Solovey, M1
Wang, Y1
Sohlbach, K1
Charles, J1
Ten Haaf, A1
Ellenrieder, V1
Gattenlöhner, S1
Bornhäuser, M2
Lim, Y1
Gondek, L1
Wang, Q1
Ma, H2
Chang, E1
Huso, DL1
Foerster, S1
Marchionni, L1
McGovern, K1
Watkins, DN1
Peacock, CD1
Merchant, AA1
Matsui, W1
Tschan-Plessl, A1
Halter, JP1
Heim, D1
Medinger, M1
Passweg, JR1
Gerull, S1
De Freitas, T1
Marktel, S1
Piemontese, S1
Carrabba, MG1
Tresoldi, C1
Messina, C1
Lupo Stanghellini, MT1
Assanelli, A1
Corti, C1
Bernardi, M1
Peccatori, J1
Vago, L1
Ciceri, F1
Muppidi, MR1
Portwood, S1
Griffiths, EA1
Thompson, JE1
Ford, LA1
Freyer, CW1
Wetzler, M1
Wang, ES1
Badar, T1
Nogueras-Gonzalez, GM1
Garcia Manero, G1
Kadia, TM1
Wierda, WG1
Patel, K1
Oran, B1
Champlin, R1
Wang, R1
Xia, L1
Gabrilove, J1
Waxman, S1
Jing, Y1
Dahl, NA1
Michaels, ST1
McMasters, RL1
Chandra, S1
O'Brien, MM1
Wang, F1
Liu, Z1
Zeng, J1
Zhu, H1
Li, J1
Cheng, X1
Jiang, T1
Zhang, L1
Zhang, C1
Chen, T1
Liu, T1
Jia, Y1
Röllig, C2
Hüttmann, A1
Baldus, CD1
Brandts, CH1
Einsele, H1
Schäfer-Eckart, K2
Krause, SW2
Mackensen, A2
Herbst, R1
Hänel, M1
Kiani, A1
Frickhofen, N1
Kullmer, J1
Kaiser, U1
Link, H1
Geer, T1
Junghanß, C2
Repp, R1
Heits, F1
Dürk, H1
Hase, J1
Klut, IM1
Illmer, T2
Parmentier, S1
Görner, M1
Schetelig, J1
Kramer, M2
Mihaila, RG1
Tavil, B1
Isgandarova, F1
Bayhan, T1
Unal, S1
Kuskonmaz, B1
Gumruk, F1
Cetin, M1
Ernst, J1
Schäfer, V1
Rinke, J1
Wittig, S1
Beck, JF1
Ernst, T1
Gruhn, B1
Lindblad, O1
Cordero, E1
Puissant, A1
Macaulay, L1
Ramos, A1
Kabir, NN1
Vallon-Christersson, J1
Haraldsson, K1
Hemann, MT1
Borg, Å1
Levander, F1
Stegmaier, K1
Pietras, K1
Rönnstrand, L1
Kazi, JU1
Gu, B1
Chen, GH1
Shen, HJ1
Ma, X1
Fu, CC1
Han, Y1
Tang, XW1
Miao, M1
Qiu, HY1
Sun, AN1
Wu, DP1
Fan, Z1
Jiang, Q1
Gao, Y1
Liu, Q1
Greenblatt, SM1
Shirley, CM1
Duffield, AS1
Nguyen, B1
Jung, E1
Aplan, PD1
Ghiaur, G1
Huang, A1
Ju, HQ1
Liu, K1
Zhan, G1
Liu, D1
Wen, S1
Huang, P1
Hu, Y1
Liu, XS1
Long, H1
Huang, YX1
Xu, JH1
Zhu, JY1
DU, QF1
Wu, BY1
Dovey, OM1
Chen, B1
Mupo, A1
Friedrich, M1
Grove, CS1
Cooper, JL1
Lee, B1
Varela, I1
Huang, Y2
Vassiliou, GS1
Yi, H1
Zeng, D1
Shen, Z1
Liao, J1
Zhang, X1
Kong, P1
Smith, AM1
Dun, MD1
Lee, EM1
Harrison, C1
Kahl, R1
Flanagan, H1
Panicker, N1
Mashkani, B1
Don, AS1
Morris, J1
Toop, H1
Powell, JA1
Guthridge, MA1
Moore, A1
Ashman, LK1
Skelding, KA1
Enjeti, A1
Verrills, NM1
Brunner, AM1
Wadleigh, M1
Collier, K1
Ballen, KK1
Cutler, CS1
Nikiforow, S1
Koreth, J1
Deangelo, DJ1
Alyea, EP1
Stone, RM1
Soiffer, RJ1
Zu, YL1
Zhang, YL1
Zhou, J1
Han, LJ1
Zhao, HF1
Gui, RR1
Hou, YJ1
Osone, S1
Imamura, T1
Kanayama, T1
Tsuma, Y1
Kawashima-Goto, S1
Nakatani, T1
Sugimoto, A1
Takai, A1
Miyachi, M1
Tamura, S1
Ishida, H1
Hosoi, H1
Ho, ES1
He, BL1
Wong, WW1
Cher, CY1
Ng, NK1
Cheung, AM2
Ip, HW1
So, CC1
Tamburini, J1
So, CW1
Ho, DN1
Au, CH1
Chan, TL1
Ma, ES1
Liang, R1
Hu, J1
Ying, SW1
Han, XY1
Zheng, YL1
Huang, H1
Mahdi, AJ1
Gosrani, D1
Chakraborty, M1
Rees, A1
Conner, C1
Wilson, K1
Rayment, R1
Alvares, C1
Fleischmann, M1
Schnetzke, U1
Schrenk, KG1
Schmidt, V1
Sayer, HG1
Hilgendorf, I1
Hochhaus, A2
Kowolik, CM1
Lin, M1
Xie, J1
Overman, LE1
Horne, DA1
Rautenberg, C1
Nachtkamp, K1
Dienst, A2
Schmidt, PV1
Heyn, C1
Kondakci, M1
Germing, U1
Haas, R3
Sid, S1
Rey, J1
Charbonnier, A1
D'Incan, E1
Mohty, B1
Blaise, D1
Vey, N1
Safaian, NN2
Czibere, A2
Bruns, I2
Fenk, R2
Reinecke, P1
Mori, S1
Andreef, M1
Zarrinkar, PP1
Gunawardane, RN1
Cramer, MD1
Gardner, MF1
Brigham, D1
Belli, B1
Karaman, MW1
Pallares, G1
Chao, Q1
Sprankle, KG1
Patel, HK1
Armstrong, RC1
James, J1
Bhagwat, SS1
Lee, SH1
Paietta, E1
Racevskis, J1
Wiernik, PH1
Sato, T2
Murphy, KM1
Stine, A2
Büchner, T1
Jones, D2
Konopleva, MY1
Pierce, SR1
Byrd, A1
Bekele, BN1
Fesler, MJ2
Richart, JM1
Petruska, PJ1
Cho, E1
Gore, SD1
McDevitt, M1
Zhao, M1
Carducci, MA1
Winkler, J1
Rech, D1
Kallert, S1
Rech, J1
Meidenbauer, N1
Roesler, W1
Spies-Weisshart, B1
Klink, A1
Muegge, LO1
Fricke, HJ1
Zhao, W1
Zhang, T1
Qu, B1
Wu, X1
Meng, F1
Gu, Y1
Shu, Y1
Shen, Y1
Sun, Y1
Xu, Q1
Zohren, F1
Saure, C1
Verstovsek, S1
Mathews, S1
Sorà, F2
Chiusolo, P2
Metafuni, E2
Bellesi, S2
Giammarco, S2
Laurenti, L2
Ausoni, G1
Zini, G1
Bayer, AJ1
Mario, B1
Leone, G2
Sica, S2
Yang, X1
Knapper, S1
White, P1
Galkin, S1
Burnett, A1
Kraljacic, BC1
Arguello, M1
Amri, A1
Cormack, G1
Borden, K1
Niu, H2
Rose, C1
Panetta, JC1
Yang, S1
Pounds, S1
Fan, Y1
Calabrese, C1
Rehg, JE1
Campana, D2
Zhou, XJ1
Zhang, SJ1
Shen, YF1
Liesveld, JL1
Rosell, KE1
Bechelli, J1
Lu, C1
Messina, P1
Mulford, D1
Ifthikharuddin, JJ1
Phillips Ii, GL1
Sharma, M1
Bayraktar, UD1
Chiattone, A1
Bashir, Q1
Giralt, S1
Chen, J1
Qazilbash, M1
Kebriaei, P1
McCue, D1
de Lima, M1
Coustan-Smith, E1
Furmanski, BD1
Mascara, GP1
Heym, KM1
Christensen, R1
Onciu, M1
Shurtleff, SA1
Pounds, SB1
Pui, CH1
Ribeiro, RC1
Al-Kali, A1
Abril, C1
Za, T1
Mohan, BP1
How, GF1
Loh, Y1
Linn, YC2
Watt, TC1
Shaid, S1
Hentrich, M1
Schleyer, E1
Ritter, B1
Pflüger, KH1
Haibach, M1
Secchiero, P3
Melloni, E2
Voltan, R3
Norcio, A1
Celeghini, C2
Zauli, G3
Faisal, A1
Gonzalez de Castro, D1
Bavetsias, V1
Sun, C1
Atrash, B1
Valenti, M1
de Haven Brandon, A1
Avery, S1
Mair, D1
Mirabella, F1
Swansbury, J1
Pearson, AD1
Workman, P1
Blagg, J1
Raynaud, FI1
Eccles, SA1
Linardopoulos, S1
Fung, TK1
Ho, C1
Han, HH1
Ma, AC1
Lok, S1
Eaves, C1
Ricciardi, MR1
Scerpa, MC1
Bergamo, P1
Ciuffreda, L1
Petrucci, MT1
Chiaretti, S1
Tavolaro, S1
Mascolo, MG1
Abrams, SL1
Steelman, LS1
Tsao, T1
Marchetti, A1
Del Bufalo, D1
Cognetti, F1
Foà, R1
McCubrey, JA1
Tafuri, A1
Milella, M1
Fey, M1
Kröger, M1
Reiter, A1
Heinicke, T1
Müller, L1
Brugger, W1
Vöhringer, M1
Mori, M1
Schultheis, B1
Baldus, C1
Swords, R1
Freeman, C1
Giles, F1
Martínez-López, J1
Castro, N1
Rueda, D1
Canal, A1
Grande, C1
Ayala, R1
Ongari, M1
Tiribelli, M1
di Iasio, MG1
Lanza, F1
Tisato, V1
Tan, P1
Jin, L1
Tabe, Y1
Lu, H1
Miida, T1
Macdonald, DA1
Assouline, SE1
Brandwein, J1
Kamel-Reid, S1
Eisenhauer, EA1
Couban, S1
Caplan, S1
Foo, A1
Walsh, W1
Leber, B1
Weisberg, E1
Sattler, M1
Al-Riyami, AZ1
Hudoba, M1
Young, S1
Forrest, D1
Tong, FK1
Chow, S2
Hedley, D1
Kancha, RK1
Grundler, R1
Peschel, C1
Ruvolo, VR1
McQueen, T2
Evans, RL1
Bornmann, WG1
McCubrey, J1
Shi, YX1
Harris, D1
Ling, X1
Quintás-Cardama, A1
Hedley, DW1
Goolsby, C1
Shankey, TV1
Minkin, P1
Shimada, A1
Dahl, GV1
Rubnitz, J1
Lucas, DL2
Tanuma, S1
Davies, PJ1
Wright, DG1
Johnson, GS2
Tamulevicius, P1
Streffer, C1
Tanizawa, A1
Kubota, M1
Takimoto, T1
Akiyama, Y1
Seto, S1
Kiriyama, Y1
Mikawa, H1

Clinical Trials (11)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Phase 1 Open-label Study of KPT-9274 in Patients With Relapsed and Refractory Acute Myeloid Leukemia[NCT04914845]Phase 140 participants (Anticipated)Interventional2021-08-27Recruiting
Phase I/II Study of Sorafenib and 5-Azacitidine for the Treatment of Patients With Refractory or Relapsed Acute Leukemia and Myelodysplastic Syndrome (MDS) - (VZ-MDS-PI-0227)[NCT01254890]Phase 1/Phase 260 participants (Actual)Interventional2011-01-31Completed
Phase I Trial of Sorafenib Maintenance Therapy for Patients With FLT3-ITD AML After Allogeneic Stem Cell Transplantation[NCT01398501]Phase 122 participants (Actual)Interventional2011-08-31Completed
Multicenter, Observational Trial to Determine the Response Rate of Sorafenib and Donor Lymphocyte Infusions (DLI) Versus Best Available Treatment (BAT) in FLT3-ITD-mutant AML Relapse After Allogeneic Hematopoietic Cell Transplantation[NCT02867891]396 participants (Actual)Observational2001-03-31Completed
A Double-blind, Placebo-controlled, Randomized, Multicenter Phase-II Trial to Assess the Efficacy of Sorafenib Added to Standard Primary Therapy in Patients With Newly Diagnosed AML ≤60 Years of Age[NCT00893373]Phase 2276 participants (Actual)Interventional2009-03-31Completed
Prospective Evaluation of Sorafenib Combined With Standard Therapy in Newly Diagnosed Adult Core-binding Factor Acute Myeloid Leukemia: an Open-label , Randomised Controlled, Multicenter Phase II Trial[NCT05404516]Phase 288 participants (Anticipated)Interventional2020-01-01Recruiting
Sorafenib for Prophylaxis of Leukemia Relapse in Allogeneic Hematopoietic Stem Cell Transplant Recipients With FLT3-ITD Positive Acute Myeloid Leukemia[NCT02474290]Phase 2/Phase 3202 participants (Actual)Interventional2015-06-20Completed
Phase I Study of BAY 43-9006 (NSC 724772) in Patients With Acute Leukemias, Myelodysplastic Syndromes and Chronic Myeloid Leukemia in Blast Phase[NCT00217646]Phase 136 participants (Actual)Interventional2005-10-31Completed
A Phase II Pilot Study of VELCADE in Patients With MDS[NCT00262873]Phase 28 participants (Actual)Interventional2005-05-31Completed
A Pilot, Pharmacodynamic Correlate Trial of Sirolimus in Combination With Chemotherapy (Idarubicin, Cytarabine) for the Treatment of Newly Diagnosed Acute Myelogenous Leukemia[NCT01822015]Early Phase 155 participants (Actual)Interventional2013-03-15Completed
A Phase II Study of Azacitidine and Sirolimus for the Treatment of High Risk Myelodysplastic Syndrome or Acute Myeloid Leukemia Refractory to or Not Eligible for Intensive Chemotherapy[NCT01869114]Phase 257 participants (Actual)Interventional2013-07-08Active, not recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Phase I: Maximum Tolerated Dose (MTD) of Sorafenib Given With Azacitidine

MTD is defined as highest dose level in which 6 patients treated with at most 1 experiencing a dose limiting toxicity (DLT) during 1st cycle. One cycle of therapy is 7 days of azacitidine (AZA) and 28 days of sorafenib. Starting dose of Sorafenib is 200 mg twice a day azacitidine (NCT01254890)
Timeframe: 28 day cycle

Interventionmg/twice daily (Number)
Azacitidine + Sorafenib400

Phase II: Number of Participants With Response

Response according to International Working Group response criteria for Acute myeloid leukemia (AML) (JCO 2003; 21: 4642-9): CR defined by presence of <5% blasts in the bone marrow (BM), with >1 X 10^9/L neutrophils and >100 x 10^9/L platelets in the peripheral blood (PB) with no detectable extramedullary disease. Participants who met the above criteria but had neutrophil or platelet counts less than the stated values were considered to have achieved CRi (CR with incomplete recovery of PB counts) or CR with incomplete platelet recovery (CRp) if CR but platelets < 100 x 10^9/L but ≥ 50 x 10^9/L and platelet transfusion independent. Partial response (PR) required all of the hematologic values for a CR but with a decrease of >/= 50% in the percentage of blasts to 5% to 25% in the BM aspirate. (NCT01254890)
Timeframe: 90 days

Interventionparticipants (Number)
Complete Response (CR)Complete Remission Without Platelet Recovery (CRi)Partial ResponseComplete Response (CRp)No Response
Azacitidine + Sorafenib8101623

Number of Participants Who Experienced an Adverse Event

(NCT00262873)
Timeframe: For 21 days/course for up to 12 courses

Interventionparticipants (Number)
Bortezomib6

Average Number of Colony Forming Unit-granulocyte-macrophages in Bone Marrow

Colony forming unit-granulocyte-macrophage (CFU-GM) progenitors, erythroid burst forming units (BFU-E), and leukemia colony forming units (CFU-L) were measured at day 0 and day 14 of cycle 1. Five × 10(4) light density cell for granulocyte-macrophage colony forming unit (CFU-GM) or erythroid burst forming unit (BFU-E) assays were plated in 0.9% methylcellulose, 30% FCS, 2 mmol/L L-glutamine, 10-4 mol/L β-mercaptoethanol, and 1% BSA with 3U/ml human erythropoietin, 10 ng/ml GM-CSF, 10 ng/ml IL-3, and 50 ng/ml stem cell factor (SCF) (c-kit ligand). For leukemia colony forming units (CFU-Ls), the plating mixture was comparable with the exception that the cytokines utilized were 4 U/ml erythropoietin, 10 ng/ml GM-CSF, 10 ng/ml IL-3, 100 ng/ml c-kit ligand, and 100 ng/ml Flt3 ligand. The methylcellulose mixture and associated reagents were purchased from Stem Cell Technologies (Vancouver, BC). Colonies were scored at Day 14 and were defined as > 20 grouped cells. (NCT00262873)
Timeframe: day 14

Interventionnumber of colonies per 50000 cell plated (Mean)
pre bortezomibpost bortezomib
Bortezomib16.128.6

Average Number of Erthroid Burst Forming Units in Bone Marrow

Colony forming unit-granulocyte-macrophage (CFU-GM) progenitors, erythroid burst forming units (BFU-E), and leukemia colony forming units (CFU-L) were measured at day 0 and day 14 of cycle 1. Five × 10(4) light density cell for granulocyte-macrophage colony forming unit (CFU-GM) or erythroid burst forming unit (BFU-E) assays were plated in 0.9% methylcellulose, 30% FCS, 2 mmol/L L-glutamine, 10-4 mol/L β-mercaptoethanol, and 1% BSA with 3U/ml human erythropoietin, 10 ng/ml GM-CSF, 10 ng/ml IL-3, and 50 ng/ml stem cell factor (SCF) (c-kit ligand). For leukemia colony forming units (CFU-Ls), the plating mixture was comparable with the exception that the cytokines utilized were 4 U/ml erythropoietin, 10 ng/ml GM-CSF, 10 ng/ml IL-3, 100 ng/ml c-kit ligand, and 100 ng/ml Flt3 ligand. The methylcellulose mixture and associated reagents were purchased from Stem Cell Technologies (Vancouver, BC). Colonies were scored at Day 14 and were defined as > 20 grouped cells. (NCT00262873)
Timeframe: day 14

Interventionnumber of colonies per 50000 cell plated (Mean)
pre bortezomibpost bortezomib
Bortezomib14.7514.75

Average Number of Leukemia Forming Units in Bone Marrow

Colony forming unit-granulocyte-macrophage (CFU-GM) progenitors, erythroid burst forming units (BFU-E), and leukemia colony forming units (CFU-L) were measured at day 0 and day 14 of cycle 1. Five × 10(4) light density cell for granulocyte-macrophage colony forming unit (CFU-GM) or erythroid burst forming unit (BFU-E) assays were plated in 0.9% methylcellulose, 30% FCS, 2 mmol/L L-glutamine, 10-4 mol/L β-mercaptoethanol, and 1% BSA with 3U/ml human erythropoietin, 10 ng/ml GM-CSF, 10 ng/ml IL-3, and 50 ng/ml stem cell factor (SCF) (c-kit ligand). For leukemia colony forming units (CFU-Ls), the plating mixture was comparable with the exception that the cytokines utilized were 4 U/ml erythropoietin, 10 ng/ml GM-CSF, 10 ng/ml IL-3, 100 ng/ml c-kit ligand, and 100 ng/ml Flt3 ligand. The methylcellulose mixture and associated reagents were purchased from Stem Cell Technologies (Vancouver, BC). Colonies were scored at Day 14 and were defined as > 20 grouped cells. (NCT00262873)
Timeframe: day 14

Interventionnumber of colonies per 50000 cell plated (Mean)
pre bortezomibpost bortezomib
Bortezomib27.6554.28

Average Percentage of Light Density Cells in Apoptosis

The CD34+ fraction of light density marrow obtained from patients at baseline and while receiving bortezomib were assessed through measurement of Annexin V (assay obtained form R&D Systems) and by flow cytometry analysis. (NCT00262873)
Timeframe: day 14

Interventionpercentage of apoptotic cells (Mean)
pre bortezomibpost bortezomib
Bortezomib6.6811.37

Interleukin 6 Levels in Serum

"interleukin-6 levels were measured by enzyme-linked immunosorbant assay ELISA in serum from participants exposed to bortezomib.~Levels were measured at Day 0 and Day 14 of cycle 1 of the clinical trial." (NCT00262873)
Timeframe: day 14

Interventionpg/ml (Mean)
pre bortezomibpost bortezomib
Bortezomib6.88.6

Vascular Endothelial Growth Factor (VEGF) Levels in Serum

VEGF levels were measured by ELISA (R&DSystems) in serum from participants exposed to bortezomib. Levels were measured at Day 0 and Day 14 of cycle 1 of the clinical trial. (NCT00262873)
Timeframe: day 14

Interventionpg/ml (Mean)
pre bortezomibpost bortezomib
Bortezomib402254

Reviews

14 reviews available for niacinamide and Acute Myelogenous Leukemia

ArticleYear
Rapid induction of complete molecular remission by sequential therapy with LDAC and sorafenib in FLT3-ITD-positive patients unfit for intensive treatment: two cases and review of the literature.
    Journal of hematology & oncology, 2013, Jun-11, Volume: 6

    Topics: Aged; Antibody Specificity; Antineoplastic Combined Chemotherapy Protocols; Cytarabine; Female; fms-

2013
Allogeneic stem cell transplantation and targeted therapy for FLT3/ITD+ acute myeloid leukemia: an update.
    Expert review of hematology, 2014, Volume: 7, Issue:2

    Topics: Carbazoles; Drug Resistance, Neoplasm; fms-Like Tyrosine Kinase 3; Furans; Hematopoietic Stem Cell T

2014
Investigational FMS-like tyrosine kinase 3 inhibitors in treatment of acute myeloid leukemia.
    Expert opinion on investigational drugs, 2014, Volume: 23, Issue:7

    Topics: Animals; Antineoplastic Agents; Benzimidazoles; Benzothiazoles; Drug Resistance, Neoplasm; fms-Like

2014
[Sorafenib in combination with chemotherapy as induction therapy for FLT3-ITD positive acute myeloid leukemia:nine cases report and literatures review].
    Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2015, Volume: 36, Issue:3

    Topics: Humans; Leukemia, Myeloid, Acute; Niacinamide; Phenylurea Compounds; Sorafenib

2015
Hypertension and Life-Threatening Bleeding in Children with Relapsed Acute Myeloblastic Leukemia Treated with FLT3 Inhibitors.
    Turkish journal of haematology : official journal of Turkish Society of Haematology, 2015, Volume: 32, Issue:3

    Topics: Acidosis; Acute Kidney Injury; Adenine Nucleotides; Antineoplastic Combined Chemotherapy Protocols;

2015
A minireview on NHE1 inhibitors. A rediscovered hope in oncohematology.
    Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia, 2015, Volume: 159, Issue:4

    Topics: Amiloride; Antineoplastic Agents; Apoptosis; Cation Transport Proteins; Cell Line, Tumor; DNA Damage

2015
Potential role of sorafenib in the treatment of acute myeloid leukemia.
    Leukemia & lymphoma, 2008, Volume: 49, Issue:12

    Topics: Benzenesulfonates; Drug Delivery Systems; Humans; Leukemia, Myeloid, Acute; Niacinamide; Phenylurea

2008
Maintenance therapy in acute myeloid leukemia revisited: will new agents rekindle an old interest?
    Current opinion in hematology, 2010, Volume: 17, Issue:2

    Topics: Azacitidine; Benzenesulfonates; Decitabine; Enzyme Inhibitors; Humans; Leukemia, Myeloid, Acute; Nia

2010
[Progression of sorafenib in the treatment of acute myeloid leukemia].
    Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2011, Volume: 32, Issue:5

    Topics: Antineoplastic Agents; Benzenesulfonates; Humans; Leukemia, Myeloid, Acute; Niacinamide; Phenylurea

2011
Molecular targeted therapy in acute myeloid leukemia.
    Hematology (Amsterdam, Netherlands), 2012, Volume: 17 Suppl 1

    Topics: Animals; Antineoplastic Agents; Benzenesulfonates; Benzothiazoles; fms-Like Tyrosine Kinase 3; Human

2012
Targeting the FMS-like tyrosine kinase 3 in acute myeloid leukemia.
    Leukemia, 2012, Volume: 26, Issue:10

    Topics: Benzenesulfonates; Benzothiazoles; Carbazoles; CCAAT-Enhancer-Binding Protein-alpha; fms-Like Tyrosi

2012
State of the art of the therapeutic perspective of sorafenib against hematological malignancies.
    Current medicinal chemistry, 2012, Volume: 19, Issue:28

    Topics: Apoptosis; Clinical Trials as Topic; fms-Like Tyrosine Kinase 3; Hematologic Neoplasms; Humans; Leuk

2012
FLT3 kinase inhibitors in the management of acute myeloid leukemia.
    Clinical lymphoma & myeloma, 2007, Volume: 8 Suppl 1

    Topics: Benzenesulfonates; Carbazoles; Clinical Trials as Topic; fms-Like Tyrosine Kinase 3; Furans; Humans;

2007
Pharmacodynamic monitoring of molecular-targeted agents in the peripheral blood of leukemia patients using flow cytometry.
    Toxicologic pathology, 2008, Volume: 36, Issue:1

    Topics: Antineoplastic Agents; Benzenesulfonates; Clinical Trials, Phase I as Topic; Drug Monitoring; Flow C

2008
Pharmacodynamic monitoring of molecular-targeted agents in the peripheral blood of leukemia patients using flow cytometry.
    Toxicologic pathology, 2008, Volume: 36, Issue:1

    Topics: Antineoplastic Agents; Benzenesulfonates; Clinical Trials, Phase I as Topic; Drug Monitoring; Flow C

2008
Pharmacodynamic monitoring of molecular-targeted agents in the peripheral blood of leukemia patients using flow cytometry.
    Toxicologic pathology, 2008, Volume: 36, Issue:1

    Topics: Antineoplastic Agents; Benzenesulfonates; Clinical Trials, Phase I as Topic; Drug Monitoring; Flow C

2008
Pharmacodynamic monitoring of molecular-targeted agents in the peripheral blood of leukemia patients using flow cytometry.
    Toxicologic pathology, 2008, Volume: 36, Issue:1

    Topics: Antineoplastic Agents; Benzenesulfonates; Clinical Trials, Phase I as Topic; Drug Monitoring; Flow C

2008

Trials

17 trials available for niacinamide and Acute Myelogenous Leukemia

ArticleYear
Phase 2 study of azacytidine plus sorafenib in patients with acute myeloid leukemia and FLT-3 internal tandem duplication mutation.
    Blood, 2013, Jun-06, Volume: 121, Issue:23

    Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Azacitidine; Feasibi

2013
Sorafenib in combination with intensive chemotherapy in elderly patients with acute myeloid leukemia: results from a randomized, placebo-controlled trial.
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2013, Sep-01, Volume: 31, Issue:25

    Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Double-Blind Method; Female

2013
Reasons for non-completion of health related quality of life evaluations in pediatric acute myeloid leukemia: a report from the Children's Oncology Group.
    PloS one, 2013, Volume: 8, Issue:9

    Topics: Adolescent; Boronic Acids; Bortezomib; Child; Child, Preschool; Female; Group Processes; Hematopoiet

2013
Final report of phase II study of sorafenib, cytarabine and idarubicin for initial therapy in younger patients with acute myeloid leukemia.
    Leukemia, 2014, Volume: 28, Issue:7

    Topics: Antineoplastic Combined Chemotherapy Protocols; Cytarabine; Humans; Idarubicin; Leukemia, Myeloid, A

2014
Phase I trial of maintenance sorafenib after allogeneic hematopoietic stem cell transplantation for fms-like tyrosine kinase 3 internal tandem duplication acute myeloid leukemia.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2014, Volume: 20, Issue:12

    Topics: Adult; Aged; Allografts; Disease-Free Survival; Female; fms-Like Tyrosine Kinase 3; Graft vs Host Di

2014
Addition of sorafenib versus placebo to standard therapy in patients aged 60 years or younger with newly diagnosed acute myeloid leukaemia (SORAML): a multicentre, phase 2, randomised controlled trial.
    The Lancet. Oncology, 2015, Volume: 16, Issue:16

    Topics: Adult; Age Factors; Antibiotics, Antineoplastic; Antimetabolites, Antineoplastic; Antineoplastic Com

2015
Addition of sorafenib versus placebo to standard therapy in patients aged 60 years or younger with newly diagnosed acute myeloid leukaemia (SORAML): a multicentre, phase 2, randomised controlled trial.
    The Lancet. Oncology, 2015, Volume: 16, Issue:16

    Topics: Adult; Age Factors; Antibiotics, Antineoplastic; Antimetabolites, Antineoplastic; Antineoplastic Com

2015
Addition of sorafenib versus placebo to standard therapy in patients aged 60 years or younger with newly diagnosed acute myeloid leukaemia (SORAML): a multicentre, phase 2, randomised controlled trial.
    The Lancet. Oncology, 2015, Volume: 16, Issue:16

    Topics: Adult; Age Factors; Antibiotics, Antineoplastic; Antimetabolites, Antineoplastic; Antineoplastic Com

2015
Addition of sorafenib versus placebo to standard therapy in patients aged 60 years or younger with newly diagnosed acute myeloid leukaemia (SORAML): a multicentre, phase 2, randomised controlled trial.
    The Lancet. Oncology, 2015, Volume: 16, Issue:16

    Topics: Adult; Age Factors; Antibiotics, Antineoplastic; Antimetabolites, Antineoplastic; Antineoplastic Com

2015
Homoharringtonine (omacetaxine mepesuccinate) as an adjunct for FLT3-ITD acute myeloid leukemia.
    Science translational medicine, 2016, 10-05, Volume: 8, Issue:359

    Topics: Adult; Aged; Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Bone Ma

2016
Sorafenib and azacitidine as salvage therapy for relapse of FLT3-ITD mutated AML after allo-SCT.
    European journal of haematology, 2017, Volume: 98, Issue:4

    Topics: Adult; Allografts; Azacitidine; Disease-Free Survival; Female; fms-Like Tyrosine Kinase 3; Hematopoi

2017
Phase I/II study of combination therapy with sorafenib, idarubicin, and cytarabine in younger patients with acute myeloid leukemia.
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2010, Apr-10, Volume: 28, Issue:11

    Topics: Adolescent; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Benzenesulfonates; Cytarabi

2010
Phase I study of sorafenib in patients with refractory or relapsed acute leukemias.
    Haematologica, 2011, Volume: 96, Issue:1

    Topics: Adult; Aged; Aged, 80 and over; Benzenesulfonates; Female; Humans; Leukemia, Lymphocytic, Chronic, B

2011
Proteasome inhibition in myelodysplastic syndromes and acute myelogenous leukemia cell lines.
    Cancer investigation, 2011, Volume: 29, Issue:7

    Topics: Antineoplastic Agents; Apoptosis; Arsenic Trioxide; Arsenicals; Azacitidine; Benzenesulfonates; Boro

2011
Phase I pharmacokinetic and pharmacodynamic study of the multikinase inhibitor sorafenib in combination with clofarabine and cytarabine in pediatric relapsed/refractory leukemia.
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2011, Aug-20, Volume: 29, Issue:24

    Topics: Adenine Nucleotides; Adolescent; Antineoplastic Combined Chemotherapy Protocols; Arabinonucleosides;

2011
Sorafenib treatment of FLT3-ITD(+) acute myeloid leukemia: favorable initial outcome and mechanisms of subsequent nonresponsiveness associated with the emergence of a D835 mutation.
    Blood, 2012, May-31, Volume: 119, Issue:22

    Topics: Adult; Aldehyde Dehydrogenase; Aldehyde Dehydrogenase 1 Family; Animals; Antineoplastic Agents; Benz

2012
The sorafenib plus nutlin-3 combination promotes synergistic cytotoxicity in acute myeloid leukemic cells irrespectively of FLT3 and p53 status.
    Haematologica, 2012, Volume: 97, Issue:11

    Topics: Antineoplastic Agents; Drug Synergism; Female; fms-Like Tyrosine Kinase 3; HL-60 Cells; Humans; Imid

2012
A phase I/II study of sorafenib in combination with low dose cytarabine in elderly patients with acute myeloid leukemia or high-risk myelodysplastic syndrome from the National Cancer Institute of Canada Clinical Trials Group: trial IND.186.
    Leukemia & lymphoma, 2013, Volume: 54, Issue:4

    Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Cytarabine; Female; fms-Lik

2013
Pharmacodynamic monitoring of BAY 43-9006 (Sorafenib) in phase I clinical trials involving solid tumor and AML/MDS patients, using flow cytometry to monitor activation of the ERK pathway in peripheral blood cells.
    Cytometry. Part B, Clinical cytometry, 2006, Volume: 70, Issue:3

    Topics: Aged; Aged, 80 and over; Antigens, CD; Antigens, CD34; Antigens, Differentiation, Myelomonocytic; Be

2006
Pharmacodynamic monitoring of BAY 43-9006 (Sorafenib) in phase I clinical trials involving solid tumor and AML/MDS patients, using flow cytometry to monitor activation of the ERK pathway in peripheral blood cells.
    Cytometry. Part B, Clinical cytometry, 2006, Volume: 70, Issue:3

    Topics: Aged; Aged, 80 and over; Antigens, CD; Antigens, CD34; Antigens, Differentiation, Myelomonocytic; Be

2006
Pharmacodynamic monitoring of BAY 43-9006 (Sorafenib) in phase I clinical trials involving solid tumor and AML/MDS patients, using flow cytometry to monitor activation of the ERK pathway in peripheral blood cells.
    Cytometry. Part B, Clinical cytometry, 2006, Volume: 70, Issue:3

    Topics: Aged; Aged, 80 and over; Antigens, CD; Antigens, CD34; Antigens, Differentiation, Myelomonocytic; Be

2006
Pharmacodynamic monitoring of BAY 43-9006 (Sorafenib) in phase I clinical trials involving solid tumor and AML/MDS patients, using flow cytometry to monitor activation of the ERK pathway in peripheral blood cells.
    Cytometry. Part B, Clinical cytometry, 2006, Volume: 70, Issue:3

    Topics: Aged; Aged, 80 and over; Antigens, CD; Antigens, CD34; Antigens, Differentiation, Myelomonocytic; Be

2006
Mutant FLT3: a direct target of sorafenib in acute myelogenous leukemia.
    Journal of the National Cancer Institute, 2008, Feb-06, Volume: 100, Issue:3

    Topics: Animals; Antineoplastic Agents; Apoptosis; Benzenesulfonates; Cell Line, Tumor; Cell Survival; Fluor

2008

Other Studies

106 other studies available for niacinamide and Acute Myelogenous Leukemia

ArticleYear
Sorafenib maintenance after hematopoietic stem cell transplantation improves outcome of FLT3-ITD-mutated acute myeloid leukemia.
    International journal of hematology, 2022, Volume: 116, Issue:6

    Topics: fms-Like Tyrosine Kinase 3; Hematopoietic Stem Cell Transplantation; Humans; Leukemia, Myeloid, Acut

2022
[The clinical safety and efficacy of the patients of acute myeloid leukemia with FLT3-ITD positive treated with sorafenib in combination with venetoclax and azactitidine regimen].
    Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2022, 11-14, Volume: 43, Issue:11

    Topics: Antineoplastic Agents; Bridged Bicyclo Compounds, Heterocyclic; fms-Like Tyrosine Kinase 3; Humans;

2022
A Prospective Study of Peritransplant Sorafenib for Patients with FLT3-ITD Acute Myeloid Leukemia Undergoing Allogeneic Transplantation.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2020, Volume: 26, Issue:2

    Topics: fms-Like Tyrosine Kinase 3; Hematopoietic Stem Cell Transplantation; Humans; Leukemia, Myeloid, Acut

2020
Nicotinamide Metabolism Mediates Resistance to Venetoclax in Relapsed Acute Myeloid Leukemia Stem Cells.
    Cell stem cell, 2020, 11-05, Volume: 27, Issue:5

    Topics: Bridged Bicyclo Compounds, Heterocyclic; Humans; Leukemia, Myeloid, Acute; Neoplastic Stem Cells; Ni

2020
Targeting LSCs: Peeling Back the Curtain on the Metabolic Complexities of AML.
    Cell stem cell, 2020, 11-05, Volume: 27, Issue:5

    Topics: Bridged Bicyclo Compounds, Heterocyclic; Humans; Leukemia, Myeloid, Acute; Neoplastic Stem Cells; Ni

2020
Genome-wide CRISPR screen identifies regulators of MAPK and MTOR pathways mediating sorafenib resistance in acute myeloid leukemia.
    Haematologica, 2022, 01-01, Volume: 107, Issue:1

    Topics: Antineoplastic Agents; Cell Line, Tumor; Clustered Regularly Interspaced Short Palindromic Repeats;

2022
Efficacy and feasibility of sorafenib as a maintenance agent after allogeneic hematopoietic stem cell transplantation for Fms-like tyrosine kinase 3-mutated acute myeloid leukemia.
    Cancer, 2017, Aug-01, Volume: 123, Issue:15

    Topics: Adolescent; Adult; Antineoplastic Agents; Chemotherapy, Adjuvant; Disease-Free Survival; Feasibility

2017
Phosphoproteome Analysis Reveals Differential Mode of Action of Sorafenib in Wildtype and Mutated FLT3 Acute Myeloid Leukemia (AML) Cells.
    Molecular & cellular proteomics : MCP, 2017, Volume: 16, Issue:7

    Topics: Cell Line, Tumor; Cell Proliferation; Cell Survival; fms-Like Tyrosine Kinase 3; Gene Regulatory Net

2017
Midostaurin Gets FDA Nod for AML.
    Cancer discovery, 2017, Volume: 7, Issue:7

    Topics: Drug Approval; fms-Like Tyrosine Kinase 3; Humans; Leukemia, Myeloid, Acute; Niacinamide; Phenylurea

2017
Adaptation to TKI Treatment Reactivates ERK Signaling in Tyrosine Kinase-Driven Leukemias and Other Malignancies.
    Cancer research, 2017, 10-15, Volume: 77, Issue:20

    Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Benzamides; Cell Line, Tumor; Cell Prolifer

2017
Long-term survival of sorafenib-treated FLT3-ITD-positive acute myeloid leukaemia patients relapsing after allogeneic stem cell transplantation.
    European journal of cancer (Oxford, England : 1990), 2017, Volume: 86

    Topics: Adolescent; Adult; Aged; Antineoplastic Agents; Biomarkers, Tumor; Disease Progression; Disease-Free

2017
The sorafenib anti-relapse effect after alloHSCT is associated with heightened alloreactivity and accumulation of CD8+PD-1+ (CD279+) lymphocytes in marrow.
    PloS one, 2018, Volume: 13, Issue:1

    Topics: Antineoplastic Agents; Bone Marrow Cells; CD8 Antigens; Female; Hematopoietic Stem Cell Transplantat

2018
[Sorafenib combined with chemotherapy and donor lymphocyte infusion as salvage therapy in patients with FLT3-positive acute myeloid leukemia relapse after allogeneic hematopoietic stem cell transplantation].
    Zhonghua nei ke za zhi, 2018, May-01, Volume: 57, Issue:5

    Topics: Antineoplastic Agents; Combined Modality Therapy; Disease-Free Survival; fms-Like Tyrosine Kinase 3;

2018
Activity of ponatinib against clinically-relevant AC220-resistant kinase domain mutants of FLT3-ITD.
    Blood, 2013, Apr-18, Volume: 121, Issue:16

    Topics: Amino Acid Sequence; Amino Acid Substitution; Benzothiazoles; Cell Line, Tumor; Drug Resistance, Neo

2013
Simultaneous inhibition of aberrant cancer kinome using rationally designed polymer-protein core-shell nanomedicine.
    Nanomedicine : nanotechnology, biology, and medicine, 2013, Volume: 9, Issue:8

    Topics: Antineoplastic Agents; Cell Line, Tumor; Drug Delivery Systems; Everolimus; Humans; Leukemia, Myeloi

2013
Emergence of polyclonal FLT3 tyrosine kinase domain mutations during sequential therapy with sorafenib and sunitinib in FLT3-ITD-positive acute myeloid leukemia.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2013, Oct-15, Volume: 19, Issue:20

    Topics: Adolescent; Alleles; Animals; Antineoplastic Agents; Cell Line, Tumor; Child; Drug Resistance, Neopl

2013
[Sorafenib monotherapy for FLT3-ITD positive acute myeloid leukemia: a case report].
    Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2013, Volume: 34, Issue:8

    Topics: fms-Like Tyrosine Kinase 3; Humans; Leukemia, Myeloid, Acute; Male; Middle Aged; Mutation; Niacinami

2013
Crenolanib is active against models of drug-resistant FLT3-ITD-positive acute myeloid leukemia.
    Blood, 2013, Nov-21, Volume: 122, Issue:22

    Topics: Animals; Antineoplastic Agents; Benzimidazoles; Cell Line, Tumor; Cell Survival; Drug Resistance, Ne

2013
Sorafenib as monotherapy or in association with cytarabine and clofarabine for the treatment of relapsed/refractory FLT3 ITD-positive advanced acute myeloid leukemia.
    Clinical lymphoma, myeloma & leukemia, 2014, Volume: 14, Issue:1

    Topics: Adenine Nucleotides; Adult; Arabinonucleosides; Clofarabine; Cytarabine; Female; fms-Like Tyrosine K

2014
Preclinical evaluation of AMG 925, a FLT3/CDK4 dual kinase inhibitor for treating acute myeloid leukemia.
    Molecular cancer therapeutics, 2014, Volume: 13, Issue:4

    Topics: Animals; Apoptosis; Cell Cycle; Cell Line, Tumor; Cell Proliferation; Cyclin-Dependent Kinase 4; Dos

2014
A novel tescalcin-sodium/hydrogen exchange axis underlying sorafenib resistance in FLT3-ITD+ AML.
    Blood, 2014, Apr-17, Volume: 123, Issue:16

    Topics: Animals; Antineoplastic Agents; Calcium-Binding Proteins; Cation Transport Proteins; Cells, Cultured

2014
Reversal of acquired drug resistance in FLT3-mutated acute myeloid leukemia cells via distinct drug combination strategies.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2014, May-01, Volume: 20, Issue:9

    Topics: Animals; Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Cell Survival; DNA Mutational Analysis;

2014
Sorafenib plus all-trans retinoic acid for AML patients with FLT3-ITD and NPM1 mutations.
    European journal of haematology, 2014, Volume: 93, Issue:6

    Topics: Adolescent; Adult; Antineoplastic Combined Chemotherapy Protocols; Fatal Outcome; Female; fms-Like T

2014
Treatment with FLT3 inhibitor in patients with FLT3-mutated acute myeloid leukemia is associated with development of secondary FLT3-tyrosine kinase domain mutations.
    Cancer, 2014, Jul-15, Volume: 120, Issue:14

    Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Benzothiazoles; Carbazoles; DNA Mutational An

2014
Sorafenib is tolerable and improves clinical outcomes in patients with FLT3-ITD acute myeloid leukemia prior to stem cell transplant and after relapse post-transplant.
    American journal of hematology, 2014, Volume: 89, Issue:9

    Topics: Adult; Aged; Antineoplastic Agents; Female; fms-Like Tyrosine Kinase 3; Hematopoietic Stem Cell Tran

2014
Use of sorafenib for post-transplant relapse in FLT3/ITD-positive acute myelogenous leukemia: maturation induction and cytotoxic effect.
    Haematologica, 2014, Volume: 99, Issue:11

    Topics: Antineoplastic Agents; Bone Marrow; Female; fms-Like Tyrosine Kinase 3; Gene Duplication; Hematopoie

2014
Extensive Squamous Cell Carcinoma of the Skin Related to Use of Sorafenib for Treatment of FLT3-Mutant Acute Myeloid Leukemia.
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2016, Mar-10, Volume: 34, Issue:8

    Topics: Aged; Antineoplastic Agents; Carcinoma, Squamous Cell; fms-Like Tyrosine Kinase 3; Humans; Leukemia,

2016
Sorafenib priming may augment salvage chemotherapy in relapsed and refractory FLT3-ITD-positive acute myeloid leukemia.
    Blood cancer journal, 2014, Aug-08, Volume: 4

    Topics: Adolescent; Adult; Antineoplastic Agents; Female; fms-Like Tyrosine Kinase 3; Humans; Leukemia, Myel

2014
Synergistic cytotoxicity of sorafenib with busulfan and nucleoside analogs in human FMS-like tyrosine kinase 3 internal tandem duplications-positive acute myeloid leukemia cells.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2014, Volume: 20, Issue:11

    Topics: Adenine Nucleotides; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Arabinonucleosides;

2014
FLT3 and CDK4/6 inhibitors: signaling mechanisms and tumor burden in subcutaneous and orthotopic mouse models of acute myeloid leukemia.
    Journal of pharmacokinetics and pharmacodynamics, 2014, Volume: 41, Issue:6

    Topics: Animals; Benzothiazoles; Cell Line, Tumor; Cyclin-Dependent Kinase 4; Cyclin-Dependent Kinase 6; Dis

2014
Inhibition of c-Kit by tyrosine kinase inhibitors.
    Haematologica, 2015, Volume: 100, Issue:3

    Topics: Aminopyridines; Antineoplastic Agents; Benzothiazoles; Biomarkers; Bone Marrow; Cell Line, Tumor; Cl

2015
Pushing the limits: defeating leukemia stem cells by depleting telomerase.
    Cell stem cell, 2014, Dec-04, Volume: 15, Issue:6

    Topics: Animals; Humans; Indoles; Leukemia, Myeloid, Acute; Neoplastic Stem Cells; Niacinamide; Telomerase;

2014
Telomerase inhibition effectively targets mouse and human AML stem cells and delays relapse following chemotherapy.
    Cell stem cell, 2014, Dec-04, Volume: 15, Issue:6

    Topics: Animals; Apoptosis; Cell Cycle Checkpoints; Cells, Cultured; Disease Models, Animal; Gene Expression

2014
Sorafenib Maintenance Appears Safe and Improves Clinical Outcomes in FLT3-ITD Acute Myeloid Leukemia After Allogeneic Hematopoietic Cell Transplantation.
    Clinical lymphoma, myeloma & leukemia, 2015, Volume: 15, Issue:5

    Topics: Adult; Antineoplastic Agents; Combined Modality Therapy; fms-Like Tyrosine Kinase 3; Gene Duplicatio

2015
Sorafenib treatment following hematopoietic stem cell transplant in pediatric FLT3/ITD acute myeloid leukemia.
    Pediatric blood & cancer, 2015, Volume: 62, Issue:6

    Topics: Adolescent; Adult; Antineoplastic Agents; Child; fms-Like Tyrosine Kinase 3; Graft vs Host Disease;

2015
Sorafenib induces paradoxical phosphorylation of the extracellular signal-regulated kinase pathway in acute myeloid leukemia cells lacking FLT3-ITD mutation.
    Leukemia & lymphoma, 2015, Volume: 56, Issue:9

    Topics: Animals; Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Cell Proliferation; Extracellular Signa

2015
Azacitidine as post-remission consolidation for sorafenib-induced remission of Fms-like tyrosine kinase-3 internal tandem duplication positive acute myeloid leukemia.
    Haematologica, 2015, Volume: 100, Issue:7

    Topics: Animals; Antineoplastic Agents; Apoptosis; Azacitidine; Cell Line, Tumor; Drug Administration Schedu

2015
[CLAG regimen in combination with sorafenib in the treatment of refractory acute myeloid leukemia:a case report].
    Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2015, Volume: 36, Issue:4

    Topics: Antineoplastic Combined Chemotherapy Protocols; Humans; Leukemia, Myeloid, Acute; Niacinamide; Pheny

2015
Sorafenib in Relapsed AML With FMS-Like Receptor Tyrosine Kinase-3 Internal Tandem Duplication Mutation.
    Journal of the National Comprehensive Cancer Network : JNCCN, 2015, Volume: 13, Issue:5

    Topics: Aged; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; fms-Like Tyrosine Kinas

2015
NFATc1 as a therapeutic target in FLT3-ITD-positive AML.
    Leukemia, 2015, Volume: 29, Issue:7

    Topics: Apoptosis; Biomarkers, Tumor; Blotting, Western; Cell Proliferation; Cyclosporine; Drug Resistance,

2015
Integration of Hedgehog and mutant FLT3 signaling in myeloid leukemia.
    Science translational medicine, 2015, Jun-10, Volume: 7, Issue:291

    Topics: Animals; Cell Compartmentation; Cell Line, Tumor; Cell Proliferation; Cell Survival; Disease Progres

2015
Synergistic effect of sorafenib and cGvHD in patients with high-risk FLT3-ITD+AML allows long-term disease control after allogeneic transplantation.
    Annals of hematology, 2015, Volume: 94, Issue:11

    Topics: Adult; Aged; Female; fms-Like Tyrosine Kinase 3; Graft vs Host Disease; Hematopoietic Stem Cell Tran

2015
High rate of hematological responses to sorafenib in FLT3-ITD acute myeloid leukemia relapsed after allogeneic hematopoietic stem cell transplantation.
    European journal of haematology, 2016, Volume: 96, Issue:6

    Topics: Adult; Aged; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Combined Modalit

2016
Decitabine and Sorafenib Therapy in FLT-3 ITD-Mutant Acute Myeloid Leukemia.
    Clinical lymphoma, myeloma & leukemia, 2015, Volume: 15 Suppl

    Topics: Azacitidine; Cell Line, Tumor; Decitabine; Female; fms-Like Tyrosine Kinase 3; Humans; Leukemia, Mye

2015
Improvement in clinical outcome of FLT3 ITD mutated acute myeloid leukemia patients over the last one and a half decade.
    American journal of hematology, 2015, Volume: 90, Issue:11

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Analysis of Variance; Antineoplastic Agents; Female; fms

2015
Sorafenib Inhibition of Mcl-1 Accelerates ATRA-Induced Apoptosis in Differentiation-Responsive AML Cells.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2016, Mar-01, Volume: 22, Issue:5

    Topics: Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Cell Differentiation; Gene Expression Reg

2016
Azacitidine and Sorafenib Therapy in a Pediatric Patient With Refractory Acute Myeloid Leukemia With Monosomy 7 and Somatic PTPN11 Mutation.
    Pediatric blood & cancer, 2016, Volume: 63, Issue:3

    Topics: Antimetabolites, Antineoplastic; Antineoplastic Agents; Azacitidine; Child, Preschool; Chromosome De

2016
Metformin synergistically sensitizes FLT3-ITD-positive acute myeloid leukemia to sorafenib by promoting mTOR-mediated apoptosis and autophagy.
    Leukemia research, 2015, Volume: 39, Issue:12

    Topics: Adaptor Proteins, Signal Transducing; AMP-Activated Protein Kinases; Antineoplastic Agents; Apoptosi

2015
Sorafenib and novel multikinase inhibitors in AML.
    The Lancet. Oncology, 2015, Volume: 16, Issue:16

    Topics: Antineoplastic Combined Chemotherapy Protocols; Female; Humans; Leukemia, Myeloid, Acute; Male; Neoa

2015
Sorafenib-induced Posterior Reversible Encephalopathy Syndrome in a Child With FLT3-ITD-positive Acute Myeloid Leukemia.
    Journal of pediatric hematology/oncology, 2016, Volume: 38, Issue:3

    Topics: Antineoplastic Agents; Child; fms-Like Tyrosine Kinase 3; Humans; Leukemia, Myeloid, Acute; Male; Ne

2016
Continuous molecular remission and regression of side effects after discontinuation of salvage therapy with sorafenib and donor lymphocyte infusions in a young patient with relapsed AML.
    Annals of hematology, 2016, Volume: 95, Issue:6

    Topics: Alopecia; Antineoplastic Agents; Child, Preschool; Female; Humans; Leukemia, Myeloid, Acute; Lymphoc

2016
Aberrant activation of the PI3K/mTOR pathway promotes resistance to sorafenib in AML.
    Oncogene, 2016, 09-29, Volume: 35, Issue:39

    Topics: Animals; Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Cell Proliferation; Drug Resistance, Ne

2016
[Improved clinical outcome of acute myeloid leukemia with FLT3-ITD mutation treated with sorafenib].
    Zhonghua nei ke za zhi, 2016, Apr-01, Volume: 55, Issue:4

    Topics: Antineoplastic Agents; Disease-Free Survival; fms-Like Tyrosine Kinase 3; Graft vs Host Disease; Hem

2016
[Sorafenib as salvage therapy in refractory relapsed acute myeloid leukemia with positive FLT3 mutation].
    Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2016, Volume: 37, Issue:4

    Topics: Antineoplastic Agents; Disease-Free Survival; fms-Like Tyrosine Kinase 3; Graft vs Host Disease; Hem

2016
All-trans retinoic acid synergizes with FLT3 inhibition to eliminate FLT3/ITD+ leukemia stem cells in vitro and in vivo.
    Blood, 2016, 06-09, Volume: 127, Issue:23

    Topics: Animals; Cell Death; Cell Line, Tumor; Drug Resistance, Neoplasm; Drug Synergism; fms-Like Tyrosine

2016
Metabolic alterations and drug sensitivity of tyrosine kinase inhibitor resistant leukemia cells with a FLT3/ITD mutation.
    Cancer letters, 2016, 07-28, Volume: 377, Issue:2

    Topics: Angiogenesis Inhibitors; Animals; Apoptosis; Cell Line, Tumor; Cell Proliferation; Deoxyglucose; Dos

2016
[Clinical Efficacy of Sorafenib Combined with Low Dose Cytarabine for Treating Patients with FLT3+ Relapsed and Refractory Acute Myeloid Leukemia].
    Zhongguo shi yan xue ye xue za zhi, 2016, Volume: 24, Issue:2

    Topics: Cytarabine; fms-Like Tyrosine Kinase 3; Humans; Leukemia, Myeloid, Acute; Niacinamide; Phenylurea Co

2016
Identification of a germline F692L drug resistance variant in cis with Flt3-internal tandem duplication in knock-in mice.
    Haematologica, 2016, Volume: 101, Issue:8

    Topics: Animals; Benzothiazoles; Drug Resistance; fms-Like Tyrosine Kinase 3; Gene Knock-In Techniques; Germ

2016
Integrin alphavbeta3 enhances β-catenin signaling in acute myeloid leukemia harboring Fms-like tyrosine kinase-3 internal tandem duplication mutations: implications for microenvironment influence on sorafenib sensitivity.
    Oncotarget, 2016, Jun-28, Volume: 7, Issue:26

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Apoptosis; beta Catenin; Cell Line, Tumor; Cell Survival

2016
Activation of protein phosphatase 2A in FLT3+ acute myeloid leukemia cells enhances the cytotoxicity of FLT3 tyrosine kinase inhibitors.
    Oncotarget, 2016, Jul-26, Volume: 7, Issue:30

    Topics: Animals; Cell Line, Tumor; Enzyme Activation; Fingolimod Hydrochloride; fms-Like Tyrosine Kinase 3;

2016
Haematopoietic cell transplantation with and without sorafenib maintenance for patients with FLT3-ITD acute myeloid leukaemia in first complete remission.
    British journal of haematology, 2016, Volume: 175, Issue:3

    Topics: Adult; Aged; Antineoplastic Agents; Combined Modality Therapy; Female; fms-Like Tyrosine Kinase 3; H

2016
[The efficacy of sorafenib to prevent relapse in patients with FLT3-ITD mutation positive acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation].
    Zhonghua nei ke za zhi, 2016, Aug-01, Volume: 55, Issue:8

    Topics: Antineoplastic Agents; Combined Modality Therapy; Disease-Free Survival; Female; fms-Like Tyrosine K

2016
Sorafenib Therapy for Pediatric Acute Myeloid Leukemia with FMS-like Tyrosine Kinase 3-internal Tandem Duplication Mutations: 2 Case Reports.
    Journal of pediatric hematology/oncology, 2017, Volume: 39, Issue:4

    Topics: Child; Child, Preschool; Drug Administration Schedule; Female; fms-Like Tyrosine Kinase 3; Hematopoi

2017
Sorafenib-induced Thyroiditis in FMS-like Tyrosine Kinase 3-internal Tandem Duplication-mutated Acute Myeloid Leukemia.
    Chinese medical journal, 2016, 10-20, Volume: 129, Issue:20

    Topics: Adult; Female; fms-Like Tyrosine Kinase 3; Humans; Leukemia, Myeloid, Acute; Mutation; Niacinamide;

2016
Successful molecular targeted treatment of AML in pregnancy with Azacitidine and Sorafenib with no adverse fetal outcomes.
    British journal of haematology, 2018, Volume: 180, Issue:4

    Topics: Adult; Antineoplastic Combined Chemotherapy Protocols; Azacitidine; Female; Humans; Leukemia, Myeloi

2018
Outcome of FLT3-ITD-positive acute myeloid leukemia: impact of allogeneic stem cell transplantation and tyrosine kinase inhibitor treatment.
    Journal of cancer research and clinical oncology, 2017, Volume: 143, Issue:2

    Topics: Adult; Aged; Antineoplastic Agents; Disease-Free Survival; Female; fms-Like Tyrosine Kinase 3; Gene

2017
NT1721, a novel epidithiodiketopiperazine, exhibits potent in vitro and in vivo efficacy against acute myeloid leukemia.
    Oncotarget, 2016, Dec-27, Volume: 7, Issue:52

    Topics: Animals; Cell Line, Tumor; Cytarabine; DNA (Cytosine-5-)-Methyltransferase 1; Humans; Leukemia, Myel

2016
Treatment of Post-transplant Relapse of FLT3-ITD Mutated AML Using 5-Azacytidine and Sorafenib Bitherapy.
    Clinical lymphoma, myeloma & leukemia, 2017, Volume: 17, Issue:4

    Topics: Antineoplastic Combined Chemotherapy Protocols; Azacitidine; fms-Like Tyrosine Kinase 3; Hematopoiet

2017
Sorafenib (Nexavar) induces molecular remission and regression of extramedullary disease in a patient with FLT3-ITD+ acute myeloid leukemia.
    Leukemia research, 2009, Volume: 33, Issue:2

    Topics: Benzenesulfonates; fms-Like Tyrosine Kinase 3; Humans; Leukemia, Myeloid, Acute; Niacinamide; Phenyl

2009
AC220 is a uniquely potent and selective inhibitor of FLT3 for the treatment of acute myeloid leukemia (AML).
    Blood, 2009, Oct-01, Volume: 114, Issue:14

    Topics: Animals; Benzenesulfonates; Benzothiazoles; Bone Marrow; Carbazoles; Cell Line, Tumor; Cell Prolifer

2009
Complete resolution of leukemia cutis with sorafenib in an acute myeloid leukemia patient with FLT3-ITD mutation.
    American journal of hematology, 2009, Volume: 84, Issue:10

    Topics: Aged; Antineoplastic Agents; Benzenesulfonates; fms-Like Tyrosine Kinase 3; Humans; Leukemia, Myeloi

2009
FLT3-mutant allelic burden and clinical status are predictive of response to FLT3 inhibitors in AML.
    Blood, 2010, Feb-18, Volume: 115, Issue:7

    Topics: Alleles; Antineoplastic Agents; Benzenesulfonates; Benzothiazoles; Carbazoles; Cell Death; Cell Line

2010
A case of blast clearance on sorafenib in relapsed FLT3-ITD acute myeloid leukemia: evidence of efficacy continues to mount.
    Leukemia research, 2010, Volume: 34, Issue:10

    Topics: Antineoplastic Agents; Benzenesulfonates; Blast Crisis; fms-Like Tyrosine Kinase 3; Humans; Leukemia

2010
A pharmacodynamic study of sorafenib in patients with relapsed and refractory acute leukemias.
    Leukemia, 2010, Volume: 24, Issue:8

    Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Benzenesulfonates; Extracellular Signal-Regul

2010
Sorafenib induces sustained molecular remission in FLT3-ITD positive AML with relapse after second allogeneic stem cell transplantation without exacerbation of acute GVHD: a case report.
    Leukemia research, 2010, Volume: 34, Issue:10

    Topics: Adult; Antineoplastic Agents; Benzenesulfonates; Female; fms-Like Tyrosine Kinase 3; Graft vs Host D

2010
Secondary resistance to sorafenib in two patients with acute myeloid leukemia (AML) harboring FLT3-ITD mutations.
    Annals of hematology, 2011, Volume: 90, Issue:4

    Topics: Aged; Antineoplastic Agents; Benzenesulfonates; Drug Resistance, Neoplasm; Fatal Outcome; fms-Like T

2011
[Sorafenib in relapsed and refractory FLT3-ITD positive acute myeloid leukemia: a novel treatment option].
    Deutsche medizinische Wochenschrift (1946), 2010, Volume: 135, Issue:38

    Topics: Adult; Aged; Antineoplastic Agents; Benzenesulfonates; Combined Modality Therapy; DNA Mutational Ana

2010
Sorafenib induces apoptosis in HL60 cells by inhibiting Src kinase-mediated STAT3 phosphorylation.
    Anti-cancer drugs, 2011, Volume: 22, Issue:1

    Topics: Apoptosis; Benzenesulfonates; Cell Cycle; Cell Growth Processes; Cell Line, Tumor; Cell Survival; DN

2011
Sorafenib treatment in 13 patients with acute myeloid leukemia and activating FLT3 mutations in combination with chemotherapy or as monotherapy.
    Acta haematologica, 2010, Volume: 124, Issue:3

    Topics: Adult; Antineoplastic Agents; Benzenesulfonates; Enzyme Activation; Female; fms-Like Tyrosine Kinase

2010
Sorafenib for refractory FMS-like tyrosine kinase receptor-3 (FLT3/ITD+) acute myeloid leukemia after allogenic stem cell transplantation.
    Leukemia research, 2011, Volume: 35, Issue:3

    Topics: Adult; Antineoplastic Agents; Benzenesulfonates; Drug Resistance, Neoplasm; fms-Like Tyrosine Kinase

2011
Marked bone marrow hypoplasia associated with sorafenib-induced marrow blast clearance in two patients with FLT3-ITD acute myeloid leukemia.
    Leukemia research, 2011, Volume: 35, Issue:3

    Topics: Aged; Antineoplastic Agents; Benzenesulfonates; Blast Crisis; Bone Marrow Diseases; fms-Like Tyrosin

2011
FLT3 ligand impedes the efficacy of FLT3 inhibitors in vitro and in vivo.
    Blood, 2011, Mar-24, Volume: 117, Issue:12

    Topics: Antineoplastic Agents; Benzenesulfonates; Carbazoles; Cells, Cultured; Drug Antagonism; fms-Like Tyr

2011
Inhibition of eIF4E with ribavirin cooperates with common chemotherapies in primary acute myeloid leukemia specimens.
    Leukemia, 2011, Volume: 25, Issue:7

    Topics: Aged; Antineoplastic Combined Chemotherapy Protocols; Benzenesulfonates; Binding, Competitive; Clini

2011
Activity of the multikinase inhibitor sorafenib in combination with cytarabine in acute myeloid leukemia.
    Journal of the National Cancer Institute, 2011, Jun-08, Volume: 103, Issue:11

    Topics: Animals; Antimetabolites, Antineoplastic; Antineoplastic Combined Chemotherapy Protocols; Apoptosis;

2011
Treatment of FLT3-ITD-positive acute myeloid leukemia relapsing after allogeneic stem cell transplantation with sorafenib.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2011, Volume: 17, Issue:12

    Topics: Adult; Aged; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Benzenesulfonate

2011
Patterns of molecular response to and relapse after combination of sorafenib, idarubicin, and cytarabine in patients with FLT3 mutant acute myeloid leukemia.
    Clinical lymphoma, myeloma & leukemia, 2011, Volume: 11, Issue:4

    Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Benzenesulfonates; Cytarabine; Female;

2011
Donor erythrocytosis induced by sorafenib treatment after allogeneic hematopoietic SCT in a patient with acute myeloid leukemia.
    Bone marrow transplantation, 2012, Volume: 47, Issue:6

    Topics: Adult; Antineoplastic Agents; Benzenesulfonates; Hematopoietic Stem Cell Transplantation; Humans; Le

2012
Sorafenib monotherapy gives sustainable suppression of FLT3 clone in untreated patients with FLT3-internal tandem duplication positive acute myeloid Leukaemia.
    British journal of haematology, 2012, Volume: 157, Issue:1

    Topics: Aged; Aged, 80 and over; Antineoplastic Agents; Female; fms-Like Tyrosine Kinase 3; Humans; Leukemia

2012
Sorafenib as treatment for relapsed or refractory pediatric acute myelogenous leukemia.
    Pediatric blood & cancer, 2012, Volume: 59, Issue:4

    Topics: Adolescent; Antineoplastic Agents; Benzenesulfonates; Child; Female; Humans; Leukemia, Myeloid, Acut

2012
Survey and analysis of the efficacy and prescription pattern of sorafenib in patients with acute myeloid leukemia.
    Leukemia & lymphoma, 2012, Volume: 53, Issue:6

    Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Benzenesulfonates; Data Collection; Female; H

2012
MCL1 down-regulation plays a critical role in mediating the higher anti-leukaemic activity of the multi-kinase inhibitor Sorafenib with respect to Dasatinib.
    British journal of haematology, 2012, Volume: 157, Issue:4

    Topics: Antineoplastic Agents; Benzenesulfonates; Cell Line, Tumor; Dasatinib; Down-Regulation; Humans; Leuk

2012
Selective FLT3 inhibition of FLT3-ITD+ acute myeloid leukaemia resulting in secondary D835Y mutation: a model for emerging clinical resistance patterns.
    Leukemia, 2012, Volume: 26, Issue:7

    Topics: Animals; Apoptosis; Aurora Kinases; Benzenesulfonates; Benzothiazoles; Blotting, Western; Cell Cycle

2012
Therapeutic potential of MEK inhibition in acute myelogenous leukemia: rationale for "vertical" and "lateral" combination strategies.
    Journal of molecular medicine (Berlin, Germany), 2012, Volume: 90, Issue:10

    Topics: Antineoplastic Agents; Apoptosis; Benzamides; Benzenesulfonates; Cell Proliferation; Cell Survival;

2012
High activity of sorafenib in FLT3-ITD-positive acute myeloid leukemia synergizes with allo-immune effects to induce sustained responses.
    Leukemia, 2012, Volume: 26, Issue:11

    Topics: Aged; Antineoplastic Agents; Benzenesulfonates; Female; fms-Like Tyrosine Kinase 3; Humans; Leukemia

2012
High activity of sorafenib in FLT3-ITD-positive acute myeloid leukemia synergizes with allo-immune effects to induce sustained responses.
    Leukemia, 2012, Volume: 26, Issue:11

    Topics: Aged; Antineoplastic Agents; Benzenesulfonates; Female; fms-Like Tyrosine Kinase 3; Humans; Leukemia

2012
High activity of sorafenib in FLT3-ITD-positive acute myeloid leukemia synergizes with allo-immune effects to induce sustained responses.
    Leukemia, 2012, Volume: 26, Issue:11

    Topics: Aged; Antineoplastic Agents; Benzenesulfonates; Female; fms-Like Tyrosine Kinase 3; Humans; Leukemia

2012
High activity of sorafenib in FLT3-ITD-positive acute myeloid leukemia synergizes with allo-immune effects to induce sustained responses.
    Leukemia, 2012, Volume: 26, Issue:11

    Topics: Aged; Antineoplastic Agents; Benzenesulfonates; Female; fms-Like Tyrosine Kinase 3; Humans; Leukemia

2012
Use of Sorafenib as an effective treatment in an AML patient carrying a new point mutation affecting the Juxtamembrane domain of FLT3.
    British journal of haematology, 2012, Volume: 158, Issue:4

    Topics: Aged; Amino Acid Sequence; Animals; Antineoplastic Agents; Benzenesulfonates; fms-Like Tyrosine Kina

2012
Limitations of targeted therapy with sorafenib in elderly high-risk myelodysplastic syndrome and acute myeloid leukemia.
    Leukemia & lymphoma, 2013, Volume: 54, Issue:4

    Topics: Female; Humans; Leukemia, Myeloid, Acute; Male; Myelodysplastic Syndromes; Niacinamide; Phenylurea C

2013
Mechanisms of apoptosis induction by simultaneous inhibition of PI3K and FLT3-ITD in AML cells in the hypoxic bone marrow microenvironment.
    Cancer letters, 2013, Feb-01, Volume: 329, Issue:1

    Topics: Antineoplastic Agents; Apoptosis; Bone Marrow; Cell Hypoxia; Cellular Microenvironment; Coculture Te

2013
A novel combination therapy approach for the treatment of acute myeloid leukemia: the multi-kinase inhibitor sorafenib and the HDM2 inhibitor nutlin-3.
    Haematologica, 2012, Volume: 97, Issue:11

    Topics: Antineoplastic Agents; Female; fms-Like Tyrosine Kinase 3; Humans; Imidazoles; Leukemia, Myeloid, Ac

2012
Sorafenib is effective for imatinib-resistant FIP1L1/PDGFRA T674I mutation-positive acute myeloid leukemia with eosinophilia.
    Leukemia & lymphoma, 2013, Volume: 54, Issue:8

    Topics: Antineoplastic Agents; Benzamides; Drug Resistance, Neoplasm; Humans; Imatinib Mesylate; Leukemia, M

2013
Sensitivity toward sorafenib and sunitinib varies between different activating and drug-resistant FLT3-ITD mutations.
    Experimental hematology, 2007, Volume: 35, Issue:10

    Topics: Antineoplastic Agents; Benzenesulfonates; Cell Line, Tumor; Drug Resistance, Neoplasm; Drug Screenin

2007
Sorafenib induces apoptosis of AML cells via Bim-mediated activation of the intrinsic apoptotic pathway.
    Leukemia, 2008, Volume: 22, Issue:4

    Topics: Apoptosis; Apoptosis Regulatory Proteins; Bcl-2-Like Protein 11; Benzenesulfonates; Cell Line; Drug

2008
Comparison of antitumor effects of multitargeted tyrosine kinase inhibitors in acute myelogenous leukemia.
    Molecular cancer therapeutics, 2008, Volume: 7, Issue:5

    Topics: Antineoplastic Agents; Apoptosis; Benzamides; Benzenesulfonates; Cell Cycle; Cell Line, Tumor; Cell

2008
Maturation of human promyelocytic leukemia cells induced by nicotinamide: evidence of a regulatory role for ADP-ribosylation of chromosomal proteins.
    Journal of cellular physiology, 1984, Volume: 121, Issue:2

    Topics: Acyltransferases; Adenosine Diphosphate Ribose; Cell Division; Cell Line; Cell Nucleus; Humans; Kine

1984
N-methylnicotinamide as a possible prognostic indicator of recovery from leukaemia in patients treated with total-body irradiation and bone marrow transplants.
    Strahlentherapie, 1984, Volume: 160, Issue:4

    Topics: Adult; Bone Marrow Transplantation; Female; Humans; Leukemia, Myeloid, Acute; Male; Niacinamide; Pro

1984
Prevention of adriamycin-induced interphase death by 3-aminobenzamide and nicotinamide in a human promyelocytic leukemia cell line.
    Biochemical and biophysical research communications, 1987, Apr-29, Volume: 144, Issue:2

    Topics: Benzamides; Cell Line; Cell Survival; DNA Damage; Doxorubicin; Humans; Interphase; Kinetics; Leukemi

1987
Formation of the N'-methylnicotinamide adenine dinucleotide derivative of NAD in intact rat pituitary tumor GH3 and human promyelocytic leukemia HL-60 cells.
    Archives of biochemistry and biophysics, 1986, Aug-15, Volume: 249, Issue:1

    Topics: Adenosine Triphosphate; Animals; Cell Line; Guanosine Triphosphate; Humans; Leukemia, Myeloid, Acute

1986