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busulfan and Chronic Disease

busulfan has been researched along with Chronic Disease in 104 studies

Chronic Disease: Diseases which have one or more of the following characteristics: they are permanent, leave residual disability, are caused by nonreversible pathological alteration, require special training of the patient for rehabilitation, or may be expected to require a long period of supervision, observation, or care (Dictionary of Health Services Management, 2d ed). For epidemiological studies chronic disease often includes HEART DISEASES; STROKE; CANCER; and diabetes (DIABETES MELLITUS, TYPE 2).

Research Excerpts

ExcerptRelevanceReference
"To reduce the incidence of graft-versus-host disease (GVHD), we added Thymoglobulin (THY) to dose-adjusted oral busulfan plus cyclophosphamide (targeted BUCY)."9.12Reduced incidence of acute and chronic graft-versus-host disease with the addition of thymoglobulin to a targeted busulfan/cyclophosphamide regimen. ( Anasetti, C; Appelbaum, FR; Boeckh, M; Deeg, HJ; Doney, KC; Flowers, ME; Hansen, JA; Heimfeld, S; Kiem, HP; Martin, PJ; McCune, JS; Myerson, D; Nash, RA; O'Donnell, PV; Radich, JP; Sandmaier, BM; Scott, BL; Sorror, ML; Storb, R; Storer, BE; Warren, EH; Witherspoon, RP; Woolfrey, A, 2006)
"Eighty-three patients with various chronic myeloproliferative disorders [polycythemia vera (PV), essential thrombocytosis (ET), idiopathic myelofibrosis (IMF)] were analyzed for the occurrence of acute myeloid leukemia (AML) and myelodysplasia (MDS) during treatment with hydroxyurea (HU) alone or HU following treatment with busulphan (BU)."7.72Acute leukemia and myelodysplasia in patients with a Philadelphia chromosome negative chronic myeloproliferative disorder treated with hydroxyurea alone or with hydroxyurea after busulphan. ( Hasselbalch, HC; Nielsen, I, 2003)
" We reviewed our experience using busulfan and cyclophosphamide (CY), instead of TBI, as the preparative regimen for allogeneic BMT to study the incidence and relationship to graft-versus-host disease (GVHD) of post-treatment eosinophilia."7.69Eosinophilia after allogeneic bone marrow transplantation using the busulfan and cyclophosphamide preparative regimen. ( Bolwell, BJ; Kalaycioglu, ME, 1994)
"Clofarabine has potent antileukemia activity and its inclusion in reduced-intensity conditioning (RIC) allogeneic hematopoietic stem cell transplantation (HSCT) for acute leukemia could potentially improve outcomes."6.82Phase II Trial of Reduced-Intensity Busulfan/Clofarabine Conditioning with Allogeneic Hematopoietic Stem Cell Transplantation for Patients with Acute Myeloid Leukemia, Myelodysplastic Syndromes, and Acute Lymphoid Leukemia. ( Alyea, E; Ballen, KK; Chen, YB; Cutler, C; Dey, BR; Driscoll, J; El-Jawahri, A; Ho, VT; Hunnewell, C; Li, S; McAfee, SL; Poliquin, C; Saylor, M; Soiffer, RJ; Spitzer, TR, 2016)
"Busulfan-treated patients had an increased risk of veno-occlusive disease (VOD) of the liver (12% v 1%, P =."6.69Increased risk of chronic graft-versus-host disease, obstructive bronchiolitis, and alopecia with busulfan versus total body irradiation: long-term results of a randomized trial in allogeneic marrow recipients with leukemia. Nordic Bone Marrow Transplanta ( Jacobsen, N; Lenhoff, S; Ljungman, P; Mellander, L; Nikoskelainen, J; Parkkali, T; Remberger, M; Ringdén, O; Ruutu, T; Sallerfors, B; Vindeløv, L; Volin, L, 1999)
" For graft-versus-host disease (GVHD) prophylaxis, cyclosporine and methotrexate were administered."5.24Reduced-Intensity Conditioning with Busulfan, Fludarabine, and Antithymocyte Globulin for Hematopoietic Cell Transplantation from Unrelated or Haploidentical Family Donors in Patients with Acute Myeloid Leukemia in Remission. ( Baek, S; Choi, EJ; Choi, Y; Jeon, M; Jo, JC; Joo, YD; Kang, YA; Kang, YL; Kim, DY; Kim, H; Kim, SH; Ko, SH; Lee, JH; Lee, KH; Lee, YS; Lim, SN; Park, HS; Seol, M; Yun, SC, 2017)
"Fifty patients with high-risk hematologic malignancies, underwent an unmanipulated haploidentical bone marrow transplantation (BMT), followed by posttransplantation high-dose cyclophosphamide (PT-CY): the myeloablative (MA) conditioning consisted of thiotepa, busulfan, fludarabine (n = 35), or total body irradiation (TBI), fludarabine (n = 15)."5.17Unmanipulated haploidentical bone marrow transplantation and posttransplantation cyclophosphamide for hematologic malignancies after myeloablative conditioning. ( Bacigalupo, A; Ballerini, F; Bregante, S; Di Grazia, C; Dominietto, A; Geroldi, S; Ghiso, A; Gualandi, F; Lamparelli, T; Luchetti, S; Miglino, M; Raiola, AM; Van Lint, MT; Varaldo, R, 2013)
"To reduce the incidence of graft-versus-host disease (GVHD), we added Thymoglobulin (THY) to dose-adjusted oral busulfan plus cyclophosphamide (targeted BUCY)."5.12Reduced incidence of acute and chronic graft-versus-host disease with the addition of thymoglobulin to a targeted busulfan/cyclophosphamide regimen. ( Anasetti, C; Appelbaum, FR; Boeckh, M; Deeg, HJ; Doney, KC; Flowers, ME; Hansen, JA; Heimfeld, S; Kiem, HP; Martin, PJ; McCune, JS; Myerson, D; Nash, RA; O'Donnell, PV; Radich, JP; Sandmaier, BM; Scott, BL; Sorror, ML; Storb, R; Storer, BE; Warren, EH; Witherspoon, RP; Woolfrey, A, 2006)
"We have reported a lower incidence of acute graft-versus-host disease (aGVHD) with a novel conditioning regimen using low-dose rabbit antithymocyte globulin (ATG; Thymoglobulin [TG]) with fludarabine and intravenous busulfan (FluBuTG)."3.74Outcomes following HSCT using fludarabine, busulfan, and thymoglobulin: a matched comparison to allogeneic transplants conditioned with busulfan and cyclophosphamide. ( Agovi, MA; Bacigalupo, A; Bahlis, NJ; Ballen, K; Bredeson, CN; Brown, C; Chaudhry, MA; Horowitz, MM; Kurian, S; Muehlenbien, CE; Quinlan, D; Rizzo, JD; Russell, JA; Savoie, L; Stewart, DA; Zhang, MJ, 2008)
" In this report, we analyzed the outcome of 101 high-risk patients (70 hematologic and 31 nonhematologic malignancies) who received an HLA-identical sibling allo-SCT after RIC, including fludarabine, busulfan, and antithymocyte globulin (ATG)."3.72Graft-versus-host disease following allogeneic transplantation from HLA-identical sibling with antithymocyte globulin-based reduced-intensity preparative regimen. ( Bay, JO; Bilger, K; Blaise, D; Chabannon, C; Choufi, B; Coso, D; Faucher, C; Maraninchi, D; Mohty, M; Stoppa, AM; Tournilhac, O; Vey, N; Viens, P, 2003)
"Eighty-three patients with various chronic myeloproliferative disorders [polycythemia vera (PV), essential thrombocytosis (ET), idiopathic myelofibrosis (IMF)] were analyzed for the occurrence of acute myeloid leukemia (AML) and myelodysplasia (MDS) during treatment with hydroxyurea (HU) alone or HU following treatment with busulphan (BU)."3.72Acute leukemia and myelodysplasia in patients with a Philadelphia chromosome negative chronic myeloproliferative disorder treated with hydroxyurea alone or with hydroxyurea after busulphan. ( Hasselbalch, HC; Nielsen, I, 2003)
" Graft-versus-host disease (GVHD) prophylaxis was attempted with cyclosporine A (CYA) and methotrexate."3.70[Severe hepatic veno-occlusive disease (VOD) which was successfully treated with supportive therapy, but subsequently developed late-recurrence]. ( Hirabayashi, N; Ikeda, Y; Ishida, A; Matsuoka, S; Moriki, T; Okamoto, S; Wakui, M; Watanabe, R, 1998)
" We reviewed our experience using busulfan and cyclophosphamide (CY), instead of TBI, as the preparative regimen for allogeneic BMT to study the incidence and relationship to graft-versus-host disease (GVHD) of post-treatment eosinophilia."3.69Eosinophilia after allogeneic bone marrow transplantation using the busulfan and cyclophosphamide preparative regimen. ( Bolwell, BJ; Kalaycioglu, ME, 1994)
"Clofarabine has potent antileukemia activity and its inclusion in reduced-intensity conditioning (RIC) allogeneic hematopoietic stem cell transplantation (HSCT) for acute leukemia could potentially improve outcomes."2.82Phase II Trial of Reduced-Intensity Busulfan/Clofarabine Conditioning with Allogeneic Hematopoietic Stem Cell Transplantation for Patients with Acute Myeloid Leukemia, Myelodysplastic Syndromes, and Acute Lymphoid Leukemia. ( Alyea, E; Ballen, KK; Chen, YB; Cutler, C; Dey, BR; Driscoll, J; El-Jawahri, A; Ho, VT; Hunnewell, C; Li, S; McAfee, SL; Poliquin, C; Saylor, M; Soiffer, RJ; Spitzer, TR, 2016)
" In summary, the combination of treosulfan and fludarabine is a safe and efficient conditioning regimen."2.71Treosulfan and fludarabine: a new toxicity-reduced conditioning regimen for allogeneic hematopoietic stem cell transplantation. ( Casper, J; Dölken, G; Freund, M; Hammer, U; Hartung, G; Kiefer, T; Kleine, HD; Knauf, W; Knopp, A; Steiner, B; Wegener, R; Wilhelm, S; Wolff, D, 2004)
"Busulfan-treated patients had an increased risk of veno-occlusive disease (VOD) of the liver (12% v 1%, P =."2.69Increased risk of chronic graft-versus-host disease, obstructive bronchiolitis, and alopecia with busulfan versus total body irradiation: long-term results of a randomized trial in allogeneic marrow recipients with leukemia. Nordic Bone Marrow Transplanta ( Jacobsen, N; Lenhoff, S; Ljungman, P; Mellander, L; Nikoskelainen, J; Parkkali, T; Remberger, M; Ringdén, O; Ruutu, T; Sallerfors, B; Vindeløv, L; Volin, L, 1999)
"Development of myelofibrosis in IMF is obviously due to disease progression unrelated to stage at diagnosis and not significantly influenced by treatment modalities."2.42Therapy-related changes of the bone marrow in chronic idiopathic myelofibrosis. ( Diehl, V; Hülsemann, R; Kvasnicka, HM; Schmitt-Gräff, A; Thiele, J, 2004)
"Chronic granulocytic leukemia, chronic lymphocytic leukemia and its variants, and hairy cell leukemia are characterized by prominent organ infiltration and marrow replacement, with a course consisting of years."2.36The chronic leukemias. ( Liepman, MK, 1980)
"The most common primary cancer was acute lymphoblastic leukemia (22 patients, 31."1.56Factors predicting endocrine late effects in childhood cancer survivors from a Japanese hospital. ( Kazukawa, I; Kihara, M; Minagawa, M; Mori, K; Shimazaki, S, 2020)
"Hydroxyurea and myelosan were mostly used as cytostatic drugs while erythrocyte mass transfusions and hemoexfusions (phlebotomy)--for life-support."1.32[Choice of therapy and overall survival in patients with chronic myeloproliferative diseases]. ( Pop, VP; Rukavitsyn, OA; Seriakov, AP, 2004)
"Dyskeratosis congenita is recognized by its dermal lesions and constitutional aplastic anemia in some cases."1.30Correction of bone marrow failure in dyskeratosis congenita by bone marrow transplantation. ( Alimoghadam, K; Ghahremani, G; Ghavamzadeh, A; Jahani, M; Khodabandeh, A; Nasseri, P, 1999)
"Philadelphia chromosome-positive chronic myelogenous leukemia was diagnosed in a now 37-year old woman 16 years ago."1.30Chronic myelogenous leukemia in chronic phase for 16 years: ongoing hematological remission and late minor cytogenetic response under minimal interferon maintenance therapy. ( Fiegl, M; Jäger, U; Mitterbauer, G; Pirc-Danoewinata, H; Weltermann, A, 1999)
" Thus, targeting avoided much of the variability in BU Css seen in other studies and appears to have allowed for an increase in oral dosing from 8 mg/kg to 10."1.29Busulfan, cyclophosphamide and fractionated total body irradiation for autologous or syngeneic marrow transplantation for acute and chronic myelogenous leukemia: phase I dose escalation of busulfan based on targeted plasma levels. ( Appelbaum, FR; Bensinger, WI; Buckner, CD; Clift, R; Demirer, T; Fefer, A; Lambert, K; Sanders, J; Slattery, JT; Storb, R, 1996)
"Cancrum oris is predominantly seen in children in underdeveloped countries where widespread malnutrition, dehydration and epidemic infections are present."1.28Cancrum oris-like lesions. ( Cheng, LH; Nash, ES; Smart, K, 1991)
"Busulfan was stopped, and only supportive treatment was given."1.27Busulfan-induced sideroblastic anemia. ( Fernandez, LA; Zayed, E, 1988)
"When busulfan treatment was resumed, hematologic response and decrease of hepatomegaly and splenomegaly reoccurred."1.27Remission of chronic idiopathic myelofibrosis to busulfan treatment. ( Chang, JC; Gross, HM, 1988)
"A case of typical idiopathic myelofibrosis turning into polycythaemia vera 6 years after diagnosis is reported."1.27[Development of polycythemia vera during chronic idiopathic myelofibrosis]. ( Covaz, E; Mazzanti, G; Paladini, G; Tosato, F, 1985)
"Chronic granulocytic leukemia developed in a 59-year-old woman who had previously received a total of 21 mCi -32P for polycythemia vera."1.25Polycythemia vera treated with -32p and myleran: development of chronic granulocytic leukemia with chromosomal abnormalities in one patient. ( Sandnes, K; Staven, P; VAN DER Hagen, CB; Vogt, E, 1975)

Research

Studies (104)

TimeframeStudies, this research(%)All Research%
pre-199046 (44.23)18.7374
1990's16 (15.38)18.2507
2000's20 (19.23)29.6817
2010's18 (17.31)24.3611
2020's4 (3.85)2.80

Authors

AuthorsStudies
Xuan, L1
Dai, M1
Jiang, E1
Wang, Y1
Huang, F1
Fan, Z1
Xu, N1
Nie, D1
Liang, X1
Chen, H2
Ye, J1
Shi, P1
Liu, H1
Jin, H1
Lin, R1
Yan, C1
Zhang, Y1
Sun, J1
Han, M1
Liu, Q1
Sevrin, F1
Kolesnikov-Gauthier, H1
Cougnenc, O1
Bogart, E1
Schleiermacher, G1
Courbon, F1
Gambart, M1
Giraudet, AL1
Corradini, N1
Badel, JN1
Rault, E1
Oudoux, A1
Deley, MCL1
Valteau-Couanet, D1
Defachelles, AS1
Shimazaki, S1
Kazukawa, I1
Mori, K1
Kihara, M1
Minagawa, M1
Araqi Houssaini, L1
Hali, F1
Quessar, A1
Marnissi, F1
Chiheb, S1
Lee, KH2
Lee, JH4
Kim, DY2
Park, HS1
Choi, EJ1
Ko, SH1
Seol, M1
Lee, YS1
Kang, YA1
Jeon, M1
Baek, S1
Kang, YL1
Kim, SH2
Yun, SC1
Kim, H1
Jo, JC1
Choi, Y1
Joo, YD1
Lim, SN1
Sun, L1
Wang, N1
Chen, Y1
Tang, L1
Xing, C1
Lu, N1
Shi, Y1
Ma, Y1
Lin, F1
Yu, K1
Feng, J1
Pagliardini, T1
Castagna, L3
Harbi, S2
Porta, MD1
Rey, J2
Fürst, S3
Bramanti, S1
Saillard, C2
Legrand, F1
Maisano, V1
Faucher, C4
Granata, A3
Hospital, MA1
Lining, W1
Weiller, PJ1
Calmels, B2
Charbonnier, A2
Lemarie, C3
Chabannon, C5
Vey, N3
Mokart, D1
Blaise, D5
Devillier, R2
Kharfan-Dabaja, MA1
Anasetti, C2
Fernandez, HF1
Perkins, J1
Ochoa-Bayona, JL1
Pidala, J1
Perez, LE1
Ayala, E1
Field, T1
Alsina, M1
Nishihori, T1
Locke, F1
Pinilla-Ibarz, J1
Tomblyn, M1
Crocchiolo, R2
El-Cheikh, J2
Signori, A1
Oudin, C2
Mohty, B1
Bouabdallah, R1
Stoppa, AM2
Broussais-Guillaumot, F1
Abedin, S1
Peres, E1
Levine, JE1
Choi, S1
Yanik, G1
Couriel, DR1
Shin, SH1
Kim, JH1
Jeon, YW1
Yoon, JH1
Yahng, SA1
Lee, SE1
Choi, YS1
Lee, S2
Kim, HJ3
Min, CK2
Lee, JW2
Min, WS2
Kim, YJ2
Aldenhoven, M1
Jones, SA1
Bonney, D1
Borrill, RE1
Coussons, M1
Mercer, J1
Bierings, MB1
Versluys, B1
van Hasselt, PM1
Wijburg, FA1
van der Ploeg, AT1
Wynn, RF1
Boelens, JJ1
Piñana, JL2
Sanz, J1
Esquirol, A1
Martino, R2
Picardi, A1
Barba, P1
Parody, R1
Gayoso, J1
Montesinos, P1
Guidi, S1
Terol, MJ1
Moscardó, F1
Solano, C1
Arcese, W1
Sanz, MA1
Sierra, J2
Sanz, G1
El-Jawahri, A1
Li, S1
Ballen, KK1
Cutler, C1
Dey, BR1
Driscoll, J1
Hunnewell, C1
Ho, VT1
McAfee, SL1
Poliquin, C1
Saylor, M1
Soiffer, RJ1
Spitzer, TR1
Alyea, E1
Chen, YB1
Ravinet, A1
Cabrespine, A1
Socié, G1
Milpied, N1
Yakoub Agha, I1
Nguyen, S1
Michallet, M2
Menard, AL1
Maillard, N1
Mohty, M3
Suarez, F1
Huynh, A1
Marchand, T1
Deteix, C1
Cassuto, JP1
Maury, S1
Chevallier, P1
Reman, O1
Peffault de Latour, R1
Bay, JO3
Fuji, S1
Kim, SW1
Yano, S1
Hagiwara, S1
Nakamae, H1
Hidaka, M1
Ito, T1
Ohashi, K1
Hatanaka, K1
Takami, A1
Kurosawa, S1
Yamashita, T1
Yamaguchi, T1
Fukuda, T2
Jaiswal, SR1
Chakrabarti, A1
Chatterjee, S1
Bhargava, S1
Ray, K1
O'Donnell, P1
Chakrabarti, S1
Ji, YS1
Lee, MS1
Min, CW1
Park, SK1
Yun, J1
Kim, KH1
Kim, CK1
Lee, KT1
Won, JH1
Hong, DS1
Bredeson, CN1
Zhang, MJ2
Agovi, MA1
Bacigalupo, A2
Bahlis, NJ1
Ballen, K1
Brown, C1
Chaudhry, MA1
Horowitz, MM1
Kurian, S1
Quinlan, D1
Muehlenbien, CE1
Russell, JA1
Savoie, L1
Rizzo, JD1
Stewart, DA1
Au, BK1
Au, MA1
Chien, JW1
Law, J1
Cowan, MJ1
Dvorak, CC1
Musick, L1
Long-Boyle, JR1
Baxter-Lowe, LA1
Horn, B1
Raiola, AM1
Dominietto, A1
Ghiso, A1
Di Grazia, C1
Lamparelli, T1
Gualandi, F1
Bregante, S1
Van Lint, MT1
Geroldi, S1
Luchetti, S1
Ballerini, F1
Miglino, M1
Varaldo, R1
Shirasugi, N1
Adams, AB1
Durham, MM1
Lukacher, AE1
Xu, H1
Rees, P1
Cowan, SR1
Williams, MA1
Pearson, TC1
Larsen, CP1
Buhr, T1
Büsche, G1
Choritz, H1
Länger, F1
Kreipe, H1
Choufi, B2
Bilger, K2
Tournilhac, O1
Coso, D1
Viens, P2
Maraninchi, D2
Mineishi, S1
Kanda, Y1
Saito, T1
Nakai, K1
Makimoto, A1
Kami, M1
Tanosaki, R2
Wakasugi, H1
Tobinai, K2
Takaue, Y2
Kröger, N2
Einsele, H1
Wolff, D2
Casper, J2
Freund, M2
Derigs, G1
Wandt, H1
Schäfer-Eckart, K1
Wittkowsky, G1
Schmitz, N1
Krüger, W1
Zabelina, T2
Renges, H1
Ayuk, F1
Krüll, A1
Zander, A2
Boiron, JM1
Cahn, JY1
Gratecos, N1
Sotto, JJ1
François, S1
Fleury, J1
Gravis, G1
Viret, F1
Braud, AC1
Bardou, VJ1
Knauf, W1
Kiefer, T1
Steiner, B1
Hammer, U1
Wegener, R1
Kleine, HD1
Wilhelm, S1
Knopp, A1
Hartung, G1
Dölken, G1
Nielsen, I1
Hasselbalch, HC1
JOSEPHSEN, JO2
KLIMA, R1
BEYREDER, J1
HERZOG, E1
SHERMAN, SI2
KUZ'MIN, DS2
ROZANOVA, LM2
KISELEVA, AN2
POVERGO, NS2
VAKULENKO, AD2
DUHAMEL, G1
Thiele, J1
Kvasnicka, HM1
Schmitt-Gräff, A1
Hülsemann, R1
Diehl, V1
Schetelig, J1
Bornhäuser, M2
Kiehl, M1
Schwerdtfeger, R1
Runde, V1
Held, TK1
Thiede, C2
Fauser, AA1
Beelen, D1
Ehninger, G2
Siegert, W1
Rukavitsyn, OA1
Pop, VP1
Seriakov, AP1
Lu, DP1
Dong, L1
Wu, T1
Huang, XJ1
Han, W1
Liu, DH1
Gao, ZY1
Chen, YH1
Xu, LP1
Zhang, YC1
Ren, HY1
Li, D1
Liu, KY1
Deeg, HJ1
Storer, BE1
Boeckh, M1
Martin, PJ1
McCune, JS1
Myerson, D1
Heimfeld, S1
Flowers, ME1
Doney, KC1
Hansen, JA1
Kiem, HP1
Nash, RA1
O'Donnell, PV1
Radich, JP1
Sandmaier, BM1
Scott, BL1
Sorror, ML1
Warren, EH1
Witherspoon, RP1
Woolfrey, A1
Appelbaum, FR2
Storb, R2
Cho, BS1
Cho, SG1
Kim, SY1
Eom, KS1
Kim, DW1
Kim, CC1
Valcárcel, D1
Caballero, D1
Martin, J1
Ferra, C1
Nieto, JB1
Sampol, A1
Bernal, MT1
Vazquez, L1
Ribera, JM1
Besalduch, J1
Moraleda, JM1
Carrera, D1
Brunet, MS1
Perez-Simón, JA1
Yamasaki, S1
Heike, Y1
Mori, S1
Maruyama, D1
Kato, R1
Usui, E1
Koido, K1
Kim, S1
Teshima, T1
Molyneux, G1
Gibson, FM1
Whayman, M1
Turton, JA1
Advani, SH1
Dinshaw, KA1
Nair, CN1
Ramakrishnan, G1
Phillips, GL2
Herzig, GP1
Beschorner, WE1
Padmanabhan, K1
Subramanian, R1
Vaidyanathan, CV1
Liepman, MK1
Woodruff, RK1
Ljungman, P2
Hassan, M1
Békássy, AN1
Ringdén, O2
Oberg, G1
Ohnishi, K1
Ohno, R1
Tomonaga, M1
Kamada, N1
Onozawa, K1
Kuramoto, A1
Dohy, H1
Mizoguchi, H1
Miyawaki, S1
Tsubaki, K1
Kalaycioglu, ME1
Bolwell, BJ1
Xun, CQ1
Thompson, JS1
Jennings, CD1
Brown, SA1
Widmer, MB1
Vowels, M1
Chan, LL1
Giri, N1
Russell, S1
Lam-Po-Tang, R1
von Bueltzingsloewen, A1
Belanger, R1
Perreault, C1
Bonny, Y1
Roy, DC1
Lalonde, Y1
Boileau, J1
Kassis, J1
Lavallee, R1
Lacombe, M1
Tura, S1
Demirer, T1
Buckner, CD1
Bensinger, WI1
Sanders, J1
Lambert, K1
Clift, R1
Fefer, A1
Slattery, JT1
Arslan, O1
Akan, H1
Koç, H1
Beksaç, M1
Ilhan, O1
Ozcan, M1
Yalçín, S1
Gürman, G1
Konuk, N1
Uysal, A1
Khoroshko, ND1
Turkina, AG1
Zhuravlev, VS1
Sokolova, MA1
Mikhaĭlova, IN1
Zakharova, AV1
Domracheva, EV1
Semenova, EA1
Matsuoka, S1
Okamoto, S1
Ishida, A1
Wakui, M1
Watanabe, R1
Moriki, T1
Ikeda, Y1
Hirabayashi, N1
Ghavamzadeh, A1
Alimoghadam, K1
Nasseri, P1
Jahani, M1
Khodabandeh, A1
Ghahremani, G1
Remberger, M1
Ruutu, T1
Nikoskelainen, J1
Volin, L1
Vindeløv, L1
Parkkali, T1
Lenhoff, S1
Sallerfors, B1
Mellander, L1
Jacobsen, N1
Fiegl, M1
Mitterbauer, G1
Weltermann, A1
Pirc-Danoewinata, H1
Jäger, U1
Platzbecker, U1
Jenke, A1
Helwig, A1
Plettig, R1
Freiberg-Richter, J1
Röllig, C1
Geissler, G1
Lutterbeck, K1
Oelschlagel, U1
Taketani, T1
Kikuchi, A1
Inatomi, J1
Hanada, R1
Kawaguchi, H1
Ida, K1
Oh-Ishi, T1
Arai, T1
Kishimoto, H1
Yamamoto, K1
Atanasov, K1
Baltov, I1
Kirova, V1
Vakrilov, V1
Tzvetkova, T1
Das, KV1
Thomas, M1
Pilla, MV1
Pugsley, CA1
Forbes, IJ1
Morley, AA2
Trainor, KJ1
Seshadri, RS1
Spiers, AS4
Whittaker, JA2
Khurshid, M2
Staven, P1
VAN DER Hagen, CB1
Vogt, E1
Sandnes, K1
Liew, A1
Baikie, AG2
Barikie, AG1
Bartnall, JA1
Cox, JI1
Jacobs, P1
Dubovsky, D1
King, H1
Sealy, R1
Gunz, FW1
Nevill, TJ1
Shepherd, JD1
Reece, DE1
Barnett, MJ1
Nantel, SH1
Klingemann, HG1
Nash, ES1
Cheng, LH1
Smart, K1
Brito-Babapulle, F1
Bowcock, SJ1
Marcus, RE1
Apperley, J1
Th'ng, KH1
Dowding, C1
Rassool, F1
Guo, AP1
Catovsky, D1
Galton, DA1
Manoharan, A1
Fernandez, LA1
Zayed, E1
Chang, JC1
Gross, HM1
Paladini, G1
Tosato, F1
Mazzanti, G1
Covaz, E1
Thompson, EN1
Soothill, JF1
Resnick, M1
Myerson, RM1
Rorvik, TO1
Pietschmann, H1
Kolarz, G2
Prandota, J1
Hunstein, W1
Hughes, HR1
Salmon, M1
Orsini, A1
Giraud, F1
Perrimond, H1
Gonggryp, N1
Markum, AH1
Abdulsalam, M1
Muslichan, S1
Iskandar, W1
Hoshino, A1
Gibson, OM1
Burgess, MA1
Stanley, LG1
Koza, I1
Cerný, V1
Bohunický, L1
Hal'ko, J1
Ujházy, V1
Petrek, C1
Krizan, Z1
Olesen, J1
Videbaek, A1
Brichta, G1
Reimer, EE1
Stoiber, T1
Pietsehmann, H1
Regele, H1
Marcovitch, H1
Morowitz, DA1
Allen, LW1
Kirsner, JB1

Clinical Trials (10)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Phase I Trial of Haploidentical Natural Killer (NK) Cells in Combination With Pemetrexed in Patients With Stage IV Non-Small Cell Lung Cancer (NSCLC)[NCT03366064]Phase 15 participants (Actual)Interventional2017-11-09Completed
Allogeneic HCT From Donor-sources of Matched-sibling, Matched-unrelated, or Haploidentical-family Donors Using Uniform Conditioning Regimen of Busulfan, Fludarabine, and Antithymocyte Globulin for AML in Remission - an Observational Study[NCT03337568]110 participants (Anticipated)Observational2017-04-01Recruiting
Trial Of Double Umbilical Cord Blood Transplantation[NCT00763490]Phase 220 participants (Actual)Interventional2008-12-31Completed
The Use of Granulocyte Transfusions After Umbilical Cord Blood Transplant for Leukaemia: A Prospective, Non-randomised, Single-centre Study to Evaluate Safety and Immune Reconstitution[NCT05425043]20 participants (Anticipated)Interventional2021-09-14Recruiting
Phase I/II Study Evaluating Safety and Efficacy of Autologous Hematopoietic Stem and Progenitor Cells Genetically Modified With IDUA Lentiviral Vector Encoding for the Human α-L-iduronidase Gene for the Treatment of Patients Affected by Mucopolysaccharido[NCT03488394]Phase 1/Phase 28 participants (Actual)Interventional2018-05-11Active, not recruiting
PRO#1278: A Phase III Study of Fludarabine and Busulfan Versus Fludarabine, Busulfan and Low Dose Total Body Irradiation in Patients Receiving an Allogeneic Hematopoietic Stem Cell Transplant[NCT01366612]Phase 353 participants (Actual)Interventional2010-06-16Terminated (stopped due to Lack of Accrual)
Bone Marrow Transplantation HLA Haploidentical After a Reduced Intensity Conditioning and Prevention of GvHD Based on Post-transplant Cyclophosphamide Administration in Patients With Severe Sickle Cell Disease[NCT03240731]Phase 218 participants (Anticipated)Interventional2017-08-10Active, not recruiting
Allogeneic Stem Cell Transplantation With Alternative Donor in Treatment of Hematologic Malignancy[NCT02487069]876 participants (Actual)Interventional2015-06-30Completed
Single Arm, Open Label, Phase I Study for Dose and Schedule Finding of Decitabine in Patients With Higher-risk MDS and MDS/AML Receiving Allogeneic Stem Cell Transplantation[NCT01277484]Phase 119 participants (Actual)Interventional2011-01-31Active, not recruiting
Non-Myeloablative Allogeneic Peripheral Blood Mobilized Hematopoietic Precursor Cell Transplantation for Chronic Phase CML[NCT00001144]Phase 250 participants Interventional1999-10-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Percentage of Participants Alive at 1 Year After Transplant

One-year survival rate after transplant (NCT00763490)
Timeframe: 1 year

Interventionpercentage of participants (Number)
Double Cord Blood Tranplant40

Percentage of Patients Alive at the End of the Trial

Event Free Survival (EFS) was determined. Patients were followed up to 5 years (median time of 2.35 years). (NCT00763490)
Timeframe: 5 Years

Interventionpercentage of patients (Number)
Double Cord Blood Tranplant35

Cumulative Incidence of Neutrophil and Platelet Engraftment

The failure to achieve a neutrophil count > 500/uL or a platelet count >30.0 x 10e9 /L within 35 days of the stem cell infusion will be defined as primary engraftment failure. (NCT00763490)
Timeframe: Day 35

Interventionpercentage of participants (Number)
Cumulative incidence of platlet engraftmentCumulative incidence of neutrophil engraftment
Double Cord Blood Tranplant7389

Incidence of Acute (Grade II-IV) and Chronic Graft-vs-host Disease(GVHD)

"The percentage of patients with acute GVHD (Grade II-IV) was determined at 100 days. Patients were followed up to 5 years and the percentage of patients that developed chronic GVHD at the end of the study was tabulated.~Acute GVHD is staged and graded (grade 0-IV, where grade 0 is no involvement and involvement increases by grade) by the number and extent of organ involvement. Patients can have involvement of three organs: skin (rash/dermatitis), liver (hepatitis/jaundice), and gastrointestinal tract (abdominal pain/diarrhea)." (NCT00763490)
Timeframe: Up to 5 years

Interventionpercentage of patients (Number)
Acute GVHD (Grades II-IV)Chronic GVHD
Double Cord Blood Tranplant4035

To Compare the Relapse Rate at 1 Year of Patients With Myeloid Malignancies Receiving Each Treatment

(NCT01366612)
Timeframe: 1 year

InterventionPercent (Number)
Group 138.9
Group 218.8

Reviews

8 reviews available for busulfan and Chronic Disease

ArticleYear
Therapy-related changes of the bone marrow in chronic idiopathic myelofibrosis.
    Histology and histopathology, 2004, Volume: 19, Issue:1

    Topics: Animals; Antineoplastic Agents; Antineoplastic Agents, Alkylating; Biopsy; Bone Marrow; Busulfan; Ch

2004
Destruction of the intestinal mucosa after bone marrow transplantation and graft-versus-host disease.
    Survey and synthesis of pathology research, 1984, Volume: 3, Issue:3

    Topics: Acute Disease; Bone Marrow Transplantation; Busulfan; Chronic Disease; Combined Modality Therapy; Cy

1984
The chronic leukemias.
    The Medical clinics of North America, 1980, Volume: 64, Issue:4

    Topics: Adult; Busulfan; Chromosomes, Human, 21-22 and Y; Chronic Disease; Humans; Leukemia; Leukemia, Hairy

1980
Chronic myeloid leukaemia.
    Australian and New Zealand journal of medicine, 1981, Volume: 11, Issue:6

    Topics: Acute Disease; Adult; Bone Marrow Transplantation; Busulfan; Cell Transformation, Neoplastic; Child,

1981
The management of elderly patients with myeloproliferative disorders.
    Hematological oncology, 1993, Volume: 11 Suppl 1

    Topics: Adult; Age Factors; Aged; Bone Marrow Transplantation; Busulfan; Chronic Disease; Humans; Hydroxyure

1993
The treatment of chronic granulocytic leukaemia.
    British journal of haematology, 1976, Volume: 32, Issue:3

    Topics: Adult; Blood Transfusion; Busulfan; Cell Transformation, Neoplastic; Chronic Disease; Humans; Immuno

1976
[Chemotherapy of chronic leukemias].
    Polskie Archiwum Medycyny Wewnetrznej, 1974, Volume: 51, Issue:3

    Topics: Antineoplastic Agents; Busulfan; Chlorambucil; Chronic Disease; Cyclophosphamide; Humans; Hydroxyure

1974
[Therapeutic considerations in chronic myeloid leukemia].
    Medizinische Klinik, 1974, Mar-08, Volume: 69, Issue:10

    Topics: Busulfan; Chronic Disease; Cytarabine; Humans; Hydrocarbons, Brominated; Leukemia, Myeloid; Mannitol

1974

Trials

20 trials available for busulfan and Chronic Disease

ArticleYear
The effect of granulocyte-colony stimulating factor, decitabine, and busulfan-cyclophosphamide versus busulfan-cyclophosphamide conditioning on relapse in patients with myelodysplastic syndrome or secondary acute myeloid leukaemia evolving from myelodyspl
    The Lancet. Haematology, 2023, Volume: 10, Issue:3

    Topics: Anemia, Refractory, with Excess of Blasts; Busulfan; Chronic Disease; Cyclophosphamide; Decitabine;

2023
Phase II study of
    Pediatric blood & cancer, 2023, Volume: 70, Issue:11

    Topics: 3-Iodobenzylguanidine; Adolescent; Busulfan; Child; Child, Preschool; Chronic Disease; Humans; Melph

2023
Reduced-Intensity Conditioning with Busulfan, Fludarabine, and Antithymocyte Globulin for Hematopoietic Cell Transplantation from Unrelated or Haploidentical Family Donors in Patients with Acute Myeloid Leukemia in Remission.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2017, Volume: 23, Issue:9

    Topics: Acute Disease; Adolescent; Adult; Aged; Antilymphocyte Serum; Busulfan; Chronic Disease; Cyclophosph

2017
Reduced-Intensity Conditioning with Busulfan, Fludarabine, and Antithymocyte Globulin for Hematopoietic Cell Transplantation from Unrelated or Haploidentical Family Donors in Patients with Acute Myeloid Leukemia in Remission.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2017, Volume: 23, Issue:9

    Topics: Acute Disease; Adolescent; Adult; Aged; Antilymphocyte Serum; Busulfan; Chronic Disease; Cyclophosph

2017
Reduced-Intensity Conditioning with Busulfan, Fludarabine, and Antithymocyte Globulin for Hematopoietic Cell Transplantation from Unrelated or Haploidentical Family Donors in Patients with Acute Myeloid Leukemia in Remission.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2017, Volume: 23, Issue:9

    Topics: Acute Disease; Adolescent; Adult; Aged; Antilymphocyte Serum; Busulfan; Chronic Disease; Cyclophosph

2017
Reduced-Intensity Conditioning with Busulfan, Fludarabine, and Antithymocyte Globulin for Hematopoietic Cell Transplantation from Unrelated or Haploidentical Family Donors in Patients with Acute Myeloid Leukemia in Remission.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2017, Volume: 23, Issue:9

    Topics: Acute Disease; Adolescent; Adult; Aged; Antilymphocyte Serum; Busulfan; Chronic Disease; Cyclophosph

2017
Unrelated Donor Peripheral Blood Stem Cell Transplantation for Patients with β-Thalassemia Major Based on a Novel Conditioning Regimen.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2019, Volume: 25, Issue:8

    Topics: Acute Disease; Adult; Allografts; Antilymphocyte Serum; beta-Thalassemia; Busulfan; Child; Child, Pr

2019
Thiotepa, Fludarabine, and Busulfan Conditioning Regimen before T Cell-Replete Haploidentical Transplantation with Post-Transplant Cyclophosphamide for Acute Myeloid Leukemia: A Bicentric Experience of 100 Patients.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2019, Volume: 25, Issue:9

    Topics: Adult; Aged; Allografts; Busulfan; Chronic Disease; Cyclophosphamide; Disease-Free Survival; Female;

2019
Phase II study of CD4+-guided pentostatin lymphodepletion and pharmacokinetically targeted busulfan as conditioning for hematopoietic cell allografting.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2013, Volume: 19, Issue:7

    Topics: Acute Disease; Adult; Aged; Antineoplastic Agents; Busulfan; CD4 Lymphocyte Count; CD4-Positive T-Ly

2013
Double umbilical cord blood transplantation after novel myeloablative conditioning using a regimen of fludarabine, busulfan, and total lymphoid irradiation.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2014, Volume: 20, Issue:12

    Topics: Acute Disease; Adolescent; Adult; Aged; Busulfan; Child; Child, Preschool; Chronic Disease; Cord Blo

2014
Umbilical cord blood transplantation in adults with advanced hodgkin's disease: high incidence of post-transplant lymphoproliferative disease.
    European journal of haematology, 2016, Volume: 96, Issue:2

    Topics: Acute Disease; Adult; Antilymphocyte Serum; Busulfan; Chronic Disease; Cord Blood Stem Cell Transpla

2016
Phase II Trial of Reduced-Intensity Busulfan/Clofarabine Conditioning with Allogeneic Hematopoietic Stem Cell Transplantation for Patients with Acute Myeloid Leukemia, Myelodysplastic Syndromes, and Acute Lymphoid Leukemia.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2016, Volume: 22, Issue:1

    Topics: Adenine Nucleotides; Adult; Aged; Arabinonucleosides; Busulfan; Chronic Disease; Clofarabine; Female

2016
A prospective multicenter study of unrelated bone marrow transplants using a reduced-intensity conditioning regimen with low-dose ATG-F.
    Bone marrow transplantation, 2016, Volume: 51, Issue:3

    Topics: Adult; Aged; Allografts; Antilymphocyte Serum; Bone Marrow Transplantation; Busulfan; Chronic Diseas

2016
Haploidentical Peripheral Blood Stem Cell Transplantation with Post-Transplantation Cyclophosphamide in Children with Advanced Acute Leukemia with Fludarabine-, Busulfan-, and Melphalan-Based Conditioning.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2016, Volume: 22, Issue:3

    Topics: Acute Disease; Adolescent; Adult; Allografts; Busulfan; Child; Child, Preschool; Chronic Disease; Cy

2016
Busulfan, fludarabine, and alemtuzumab as a reduced toxicity regimen for children with malignant and nonmalignant diseases improves engraftment and graft-versus-host disease without delaying immune reconstitution.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2012, Volume: 18, Issue:11

    Topics: Adolescent; Alemtuzumab; Antibodies, Monoclonal, Humanized; B-Lymphocytes; Busulfan; Child; Child, P

2012
Unmanipulated haploidentical bone marrow transplantation and posttransplantation cyclophosphamide for hematologic malignancies after myeloablative conditioning.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2013, Volume: 19, Issue:1

    Topics: Acute Disease; Adolescent; Adult; Aged; Antineoplastic Agents; Bone Marrow Transplantation; Busulfan

2013
Myeloablative intensified conditioning regimen with in vivo T-cell depletion (ATG) followed by allografting in patients with advanced multiple myeloma. A phase I/II study of the German Study-group Multiple Myeloma (DSMM).
    Bone marrow transplantation, 2003, Volume: 31, Issue:11

    Topics: Acute Disease; Adult; Antilymphocyte Serum; Busulfan; Chronic Disease; Cyclophosphamide; Disease-Fre

2003
Treosulfan and fludarabine: a new toxicity-reduced conditioning regimen for allogeneic hematopoietic stem cell transplantation.
    Blood, 2004, Jan-15, Volume: 103, Issue:2

    Topics: Acute Disease; Adult; Aged; Alkylating Agents; Busulfan; Chronic Disease; Family; Female; Histocompa

2004
Reduced incidence of acute and chronic graft-versus-host disease with the addition of thymoglobulin to a targeted busulfan/cyclophosphamide regimen.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2006, Volume: 12, Issue:5

    Topics: Acute Disease; Adolescent; Adult; Aged; Antilymphocyte Serum; Busulfan; Cause of Death; Child; Chron

2006
The beneficial effect of chronic graft-versus-host disease on the clinical outcome of transplantation with fludarabine/busulfan-based reduced-intensity conditioning for patients with de novo myelodysplastic syndrome.
    International journal of hematology, 2007, Volume: 85, Issue:5

    Topics: Adolescent; Adult; Antineoplastic Agents; Busulfan; Chronic Disease; Female; Follow-Up Studies; Graf

2007
A randomized trial comparing interferon-alpha with busulfan for newly diagnosed chronic myelogenous leukemia in chronic phase.
    Blood, 1995, Aug-01, Volume: 86, Issue:3

    Topics: Adult; Blood Cell Count; Bone Marrow; Busulfan; Chronic Disease; Female; Humans; Interferon-alpha; L

1995
Increased risk of chronic graft-versus-host disease, obstructive bronchiolitis, and alopecia with busulfan versus total body irradiation: long-term results of a randomized trial in allogeneic marrow recipients with leukemia. Nordic Bone Marrow Transplanta
    Blood, 1999, Apr-01, Volume: 93, Issue:7

    Topics: Adolescent; Adult; Alopecia; Bone Marrow Transplantation; Bronchiolitis Obliterans; Busulfan; Catara

1999
Dose-reduced conditioning and allogeneic hematopoietic stem cell transplantation from unrelated donors in 42 patients.
    Clinical cancer research : an official journal of the American Association for Cancer Research, 2001, Volume: 7, Issue:8

    Topics: Acute Disease; Adolescent; Adult; Aged; Antilymphocyte Serum; Antineoplastic Combined Chemotherapy P

2001

Other Studies

76 other studies available for busulfan and Chronic Disease

ArticleYear
Factors predicting endocrine late effects in childhood cancer survivors from a Japanese hospital.
    Endocrine journal, 2020, Feb-28, Volume: 67, Issue:2

    Topics: Adolescent; Adult; Antineoplastic Agents; Brain Neoplasms; Busulfan; Cancer Survivors; Child; Chroni

2020
[Cutaneous complications following hematopoietic stem cell transplantation].
    Bulletin du cancer, 2021, Volume: 108, Issue:9

    Topics: Acute Disease; Adolescent; Adult; Allografts; Busulfan; Candidiasis; Chickenpox; Child; Chronic Dise

2021
National Institutes of Health classification for chronic graft-versus-host disease predicts outcome of allo-hematopoietic stem cell transplant after fludarabine-busulfan-antithymocyte globulin conditioning regimen.
    Leukemia & lymphoma, 2014, Volume: 55, Issue:5

    Topics: Adolescent; Adult; Aged; Antilymphocyte Serum; Antineoplastic Combined Chemotherapy Protocols; Busul

2014
Antithymocyte globulin in reduced-intensity conditioning regimen allows a high disease-free survival exempt of long-term chronic graft-versus-host disease.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2014, Volume: 20, Issue:3

    Topics: Adult; Aged; Antilymphocyte Serum; Antineoplastic Agents; Busulfan; Chronic Disease; Female; Graft v

2014
Feasible outcomes of T cell-replete haploidentical stem cell transplantation with reduced-intensity conditioning in patients with myelodysplastic syndrome.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2015, Volume: 21, Issue:2

    Topics: Acute Disease; Adult; Aged; Antilymphocyte Serum; Busulfan; Chronic Disease; Female; Graft vs Host D

2015
Hematopoietic cell transplantation for mucopolysaccharidosis patients is safe and effective: results after implementation of international guidelines.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2015, Volume: 21, Issue:6

    Topics: Acute Disease; Busulfan; Child; Child, Preschool; Chronic Disease; Cord Blood Stem Cell Transplantat

2015
Hematopoietic cell transplantation for mucopolysaccharidosis patients is safe and effective: results after implementation of international guidelines.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2015, Volume: 21, Issue:6

    Topics: Acute Disease; Busulfan; Child; Child, Preschool; Chronic Disease; Cord Blood Stem Cell Transplantat

2015
Hematopoietic cell transplantation for mucopolysaccharidosis patients is safe and effective: results after implementation of international guidelines.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2015, Volume: 21, Issue:6

    Topics: Acute Disease; Busulfan; Child; Child, Preschool; Chronic Disease; Cord Blood Stem Cell Transplantat

2015
Hematopoietic cell transplantation for mucopolysaccharidosis patients is safe and effective: results after implementation of international guidelines.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2015, Volume: 21, Issue:6

    Topics: Acute Disease; Busulfan; Child; Child, Preschool; Chronic Disease; Cord Blood Stem Cell Transplantat

2015
Impact of Thymoglobulin by Stem Cell Source (Peripheral Blood Stem Cell or Bone Marrow) After Myeloablative Stem Cell Transplantation From HLA 10/10-Matched Unrelated Donors: A Report From the Société Française de Greffe de Moelle et de Thérapie Cellulair
    Transplantation, 2016, Volume: 100, Issue:8

    Topics: Adolescent; Adult; Antilymphocyte Serum; Bone Marrow Transplantation; Busulfan; Chi-Square Distribut

2016
Does anti-thymocyte globulin have a place in busulfan/fludarabine conditioning for matched related donor hematopoietic stem cell transplantation?
    The Korean journal of internal medicine, 2016, Volume: 31, Issue:4

    Topics: Acute Disease; Adult; Antilymphocyte Serum; Busulfan; Chronic Disease; Disease-Free Survival; Drug T

2016
Outcomes following HSCT using fludarabine, busulfan, and thymoglobulin: a matched comparison to allogeneic transplants conditioned with busulfan and cyclophosphamide.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2008, Volume: 14, Issue:9

    Topics: Acute Disease; Adolescent; Adult; Aged; Antibodies, Monoclonal; Antilymphocyte Serum; Busulfan; Chro

2008
Bronchiolitis obliterans syndrome epidemiology after allogeneic hematopoietic cell transplantation.
    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2011, Volume: 17, Issue:7

    Topics: Adolescent; Adult; Aged; Bone Marrow Transplantation; Bronchiolitis Obliterans; Busulfan; Chronic Di

2011
Prevention of chronic rejection in murine cardiac allografts: a comparison of chimerism- and nonchimerism-inducing costimulation blockade-based tolerance induction regimens.
    Journal of immunology (Baltimore, Md. : 1950), 2002, Sep-01, Volume: 169, Issue:5

    Topics: Acute Disease; Animals; Bone Marrow Cells; Bone Marrow Transplantation; Busulfan; Chronic Disease; C

2002
Evolution of myelofibrosis in chronic idiopathic myelofibrosis as evidenced in sequential bone marrow biopsy specimens.
    American journal of clinical pathology, 2003, Volume: 119, Issue:1

    Topics: Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Bone Marrow; Busulfan; Chroni

2003
Graft-versus-host disease following allogeneic transplantation from HLA-identical sibling with antithymocyte globulin-based reduced-intensity preparative regimen.
    Blood, 2003, Jul-15, Volume: 102, Issue:2

    Topics: Acute Disease; Adolescent; Adult; Antilymphocyte Serum; Busulfan; Chronic Disease; Disease Progressi

2003
Impact of graft-versus-host disease in reduced-intensity stem cell transplantation (RIST) for patients with haematological malignancies.
    British journal of haematology, 2003, Volume: 121, Issue:2

    Topics: Acute Disease; Adolescent; Adult; Aged; Busulfan; Chronic Disease; Cladribine; Cyclophosphamide; Dis

2003
Reduced-intensity preparative regimen and allogeneic stem cell transplantation for advanced solid tumors.
    Blood, 2004, Jan-15, Volume: 103, Issue:2

    Topics: Acute Disease; Adult; Antilymphocyte Serum; Bone Marrow Transplantation; Busulfan; Chronic Disease;

2004
Acute leukemia and myelodysplasia in patients with a Philadelphia chromosome negative chronic myeloproliferative disorder treated with hydroxyurea alone or with hydroxyurea after busulphan.
    American journal of hematology, 2003, Volume: 74, Issue:1

    Topics: Acute Disease; Alkylating Agents; Busulfan; Chronic Disease; Drug Therapy, Combination; Female; Huma

2003
[Myleran in chronic myelogenic leukemia].
    Nordisk medicin, 1956, Oct-18, Volume: 56, Issue:42

    Topics: Busulfan; Chronic Disease; Humans; Leukemia; Leukemia, Myeloid

1956
[Myleran in chronic myelogenic leukemia].
    Nordisk medicin, 1956, Oct-18, Volume: 56, Issue:42

    Topics: Busulfan; Chronic Disease; Humans; Leukemia; Leukemia, Myeloid

1956
[Myleran in chronic myelogenic leukemia].
    Nordisk medicin, 1956, Oct-18, Volume: 56, Issue:42

    Topics: Busulfan; Chronic Disease; Humans; Leukemia; Leukemia, Myeloid

1956
[Myleran in chronic myelogenic leukemia].
    Nordisk medicin, 1956, Oct-18, Volume: 56, Issue:42

    Topics: Busulfan; Chronic Disease; Humans; Leukemia; Leukemia, Myeloid

1956
[Cytostatic prolonged therapy in chronic leukemia].
    Wiener medizinische Wochenschrift (1946), 1957, May-11, Volume: 107, Issue:18-19

    Topics: Busulfan; Chronic Disease; Humans; Leukemia; Leukemia, Myeloid

1957
[Comparative evaluation of the effectiveness of certain therapeutic methods in chronic leukemias; roentgen rays, radioactive phosphorus, urethane, embichine, arsenic, myleran. IV].
    Problemy gematologii i perelivaniia krovi, 1959, Volume: 4, Issue:1

    Topics: Arsenic; Busulfan; Chronic Disease; Leukemia; Phosphorus; Phosphorus, Dietary; Radioactivity; Uretha

1959
[Comparative evaluation of the effectiveness of certain therapeutic methods in chronic leukemias; roentgen rays, radioactive phosphorus, urethane, embichine, arsenic, myleran. V].
    Problemy gematologii i perelivaniia krovi, 1959, Volume: 4, Issue:5

    Topics: Arsenic; Busulfan; Chronic Disease; Leukemia; Phosphorus; Phosphorus, Dietary; Radioactivity; Uretha

1959
[CHRONIC LEUKEMIA. RECENT DATA ON ITS DIAGNOSIS AND TREATMENT].
    Concours medical, 1963, Nov-16, Volume: 85

    Topics: Busulfan; Child; Chronic Disease; Leukemia; Leukemia, Myeloid; Neoplasms

1963
Reduced-intensity conditioning with busulfan and fludarabine with or without antithymocyte globulin in HLA-identical sibling transplantation--a retrospective analysis.
    Bone marrow transplantation, 2004, Volume: 33, Issue:5

    Topics: Acute Disease; Adult; Aged; Antilymphocyte Serum; Busulfan; Chronic Disease; Combined Modality Thera

2004
[Choice of therapy and overall survival in patients with chronic myeloproliferative diseases].
    Voprosy onkologii, 2004, Volume: 50, Issue:4

    Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Antineoplastic Agents, Alkylating; Busulfan;

2004
Conditioning including antithymocyte globulin followed by unmanipulated HLA-mismatched/haploidentical blood and marrow transplantation can achieve comparable outcomes with HLA-identical sibling transplantation.
    Blood, 2006, Apr-15, Volume: 107, Issue:8

    Topics: Acute Disease; Adolescent; Adult; Antilymphocyte Serum; Antineoplastic Combined Chemotherapy Protoco

2006
Sustained remissions of high-risk acute myeloid leukemia and myelodysplastic syndrome after reduced-intensity conditioning allogeneic hematopoietic transplantation: chronic graft-versus-host disease is the strongest factor improving survival.
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2008, Feb-01, Volume: 26, Issue:4

    Topics: Adult; Aged; Busulfan; Chronic Disease; Disease-Free Survival; Drug Therapy, Combination; Female; Gr

2008
Infectious complications in chronic graft-versus-host disease: a retrospective study of 145 recipients of allogeneic hematopoietic stem cell transplantation with reduced- and conventional-intensity conditioning regimens.
    Transplant infectious disease : an official journal of the Transplantation Society, 2008, Volume: 10, Issue:4

    Topics: Adolescent; Adult; Aged; Aspergillosis; Bacteremia; Busulfan; Catheterization, Central Venous; Chron

2008
Serum FLT-3 ligand in a busulphan-induced model of chronic bone marrow hypoplasia in the female CD-1 mouse.
    International journal of experimental pathology, 2008, Volume: 89, Issue:2

    Topics: Animals; Antineoplastic Agents, Alkylating; Blood Cell Count; Body Weight; Bone Marrow Cells; Bone M

2008
Total body irradiation in chronic myeloid leukemia.
    International journal of radiation oncology, biology, physics, 1983, Volume: 9, Issue:4

    Topics: Adolescent; Adult; Busulfan; Chronic Disease; Female; Humans; Leukemia, Myeloid; Leukocyte Count; Ma

1983
Intensive chemotherapy, total body irradiation, and autologous marrow transplantation for chronic granulocytic leukemia-blast phase: report of four additional cases.
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 1984, Volume: 2, Issue:5

    Topics: Adult; Bone Marrow; Bone Marrow Transplantation; Busulfan; Child; Chromosomes, Human, 21-22 and Y; C

1984
Chronic granulocytic leukemia with lymphadenopathy and leukemia cutis.
    The Journal of the Association of Physicians of India, 1982, Volume: 30, Issue:8

    Topics: Adult; Busulfan; Chronic Disease; Female; Humans; Leukemia, Myeloid; Lymphatic Metastasis; Skin; Ski

1982
Busulfan concentration in relation to permanent alopecia in recipients of bone marrow transplants.
    Bone marrow transplantation, 1995, Volume: 15, Issue:6

    Topics: Adolescent; Adult; Alopecia; Anemia, Aplastic; Bone Marrow Transplantation; Busulfan; Child; Child,

1995
Eosinophilia after allogeneic bone marrow transplantation using the busulfan and cyclophosphamide preparative regimen.
    Bone marrow transplantation, 1994, Volume: 14, Issue:1

    Topics: Adolescent; Adult; Bone Marrow Transplantation; Busulfan; Chronic Disease; Cyclophosphamide; Eosinop

1994
Effect of total body irradiation, busulfan-cyclophosphamide, or cyclophosphamide conditioning on inflammatory cytokine release and development of acute and chronic graft-versus-host disease in H-2-incompatible transplanted SCID mice.
    Blood, 1994, Apr-15, Volume: 83, Issue:8

    Topics: Acute Disease; Animals; Busulfan; Cell Transplantation; Chronic Disease; Cyclophosphamide; Cytokines

1994
Factors affecting hair regrowth after bone marrow transplantation.
    Bone marrow transplantation, 1993, Volume: 12, Issue:4

    Topics: Adolescent; Adult; Age Factors; Alopecia; Bone Marrow Purging; Bone Marrow Transplantation; Busulfan

1993
Acute graft-versus-host disease prophylaxis with methotrexate and cyclosporine after busulfan and cyclophosphamide in patients with hematologic malignancies.
    Blood, 1993, Feb-01, Volume: 81, Issue:3

    Topics: Adult; Busulfan; Chronic Disease; Combined Modality Therapy; Cyclophosphamide; Cyclosporine; Female;

1993
Busulfan, cyclophosphamide and fractionated total body irradiation for autologous or syngeneic marrow transplantation for acute and chronic myelogenous leukemia: phase I dose escalation of busulfan based on targeted plasma levels.
    Bone marrow transplantation, 1996, Volume: 17, Issue:4

    Topics: Acute Disease; Administration, Oral; Adolescent; Adult; Busulfan; Child; Child, Preschool; Chronic D

1996
Eosinophilia after allogeneic bone marrow transplantation using busulfan and cyclophosphamide conditioning regimen.
    Bone marrow transplantation, 1996, Volume: 18, Issue:1

    Topics: Bone Marrow Transplantation; Busulfan; Chronic Disease; Cyclophosphamide; Eosinophilia; Graft vs Hos

1996
[A modern therapeutic strategy in Ph-positive chronic myeloleukemia].
    Terapevticheskii arkhiv, 1996, Volume: 68, Issue:7

    Topics: Adolescent; Adult; Antineoplastic Agents, Alkylating; Antineoplastic Combined Chemotherapy Protocols

1996
[Severe hepatic veno-occlusive disease (VOD) which was successfully treated with supportive therapy, but subsequently developed late-recurrence].
    [Rinsho ketsueki] The Japanese journal of clinical hematology, 1998, Volume: 39, Issue:2

    Topics: Adult; Bone Marrow Transplantation; Busulfan; Chronic Disease; Cyclophosphamide; Cyclosporine; Graft

1998
Correction of bone marrow failure in dyskeratosis congenita by bone marrow transplantation.
    Bone marrow transplantation, 1999, Volume: 23, Issue:3

    Topics: Adolescent; Adult; Anemia, Aplastic; Bone Marrow Transplantation; Busulfan; Chronic Disease; Cycloph

1999
Chronic myelogenous leukemia in chronic phase for 16 years: ongoing hematological remission and late minor cytogenetic response under minimal interferon maintenance therapy.
    Leukemia & lymphoma, 1999, Volume: 35, Issue:3-4

    Topics: Adult; Antineoplastic Agents; Busulfan; Chronic Disease; Cytogenetics; Female; Humans; Hydroxyurea;

1999
Chronic active Epstein-Barr virus infection (CAEBV) successfully treated with allogeneic peripheral blood stem cell transplantation.
    Bone marrow transplantation, 2002, Volume: 29, Issue:6

    Topics: Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Busulfan; Child; Chronic Dise

2002
Chronic myelosis treatment with Myleran (Myelosan).
    Folia medica, 1978, Volume: 20, Issue:1

    Topics: Adult; Busulfan; Chronic Disease; Female; Humans; Leukemia, Myeloid; Male; Middle Aged

1978
Observations on the therapy of chronic granulocytic leukaemia (C.G.L.) in adults.
    The Journal of the Association of Physicians of India, 1977, Volume: 25, Issue:8

    Topics: Adolescent; Adult; Aged; Busulfan; Child; Chronic Disease; Female; Humans; India; Leukemia, Myeloid;

1977
Immunologic abnormalities in an animal model of chronic hypoplastic marrow failure induced by busulfan.
    Blood, 1978, Volume: 51, Issue:4

    Topics: Anemia, Aplastic; Animals; Antibody-Producing Cells; B-Lymphocytes; Blood Cell Count; Busulfan; Chro

1978
Chronic hypoplastic marrow failure and residual injury.
    Blood cells, 1978, Volume: 4, Issue:1-2

    Topics: Anemia, Aplastic; Animals; Bone Marrow; Bone Marrow Transplantation; Busulfan; Cell Division; Chroni

1978
Hypofibrinogenaemia as a cause of bleeding in chronic myeloid leukaemia.
    British medical journal, 1975, Mar-01, Volume: 1, Issue:5956

    Topics: Afibrinogenemia; Aged; Blood Cell Count; Bone Marrow Cells; Busulfan; Chronic Disease; Disseminated

1975
Polycythemia vera treated with -32p and myleran: development of chronic granulocytic leukemia with chromosomal abnormalities in one patient.
    Clinical genetics, 1975, Volume: 7, Issue:3

    Topics: Anemia, Hemolytic, Autoimmune; Busulfan; Chromosomes, Human, 1-3; Chromosomes, Human, 6-12 and X; Ch

1975
Neutrophil alkaline phosphatase score in chronic granulocytic leukaemia: effects of splenectomy and antileukaemic drugs.
    Journal of clinical pathology, 1975, Volume: 28, Issue:7

    Topics: Alkaline Phosphatase; Bone Marrow Cells; Busulfan; Chronic Disease; Clinical Enzyme Tests; Histocyto

1975
Cytogenetic studies of the spleen in chronic granulocytic leukaemia.
    Australian and New Zealand journal of medicine, 1975, Volume: 5, Issue:4

    Topics: Adult; Busulfan; Cell Line; Chromosome Aberrations; Chromosomes, Human, 21-22 and Y; Chronic Disease

1975
Splenic irradiation in the management of chronic granulocytic leukaemia.
    The Central African journal of medicine, 1975, Volume: 21, Issue:10

    Topics: Adult; Aged; Busulfan; Chronic Disease; Female; Humans; Leukemia, Myeloid; Male; Middle Aged; Radiat

1975
Diagnostic and therapeutic approach to chronic leukaemia.
    Australian and New Zealand journal of medicine, 1975, Volume: 5, Issue:6

    Topics: Busulfan; Chlorambucil; Chronic Disease; Diagnosis, Differential; Glucocorticoids; Leukemia; Leukemi

1975
Treatment of myelodysplastic syndrome with busulfan-cyclophosphamide conditioning followed by allogeneic BMT.
    Bone marrow transplantation, 1992, Volume: 10, Issue:5

    Topics: Acute Disease; Adult; Age Factors; Antineoplastic Combined Chemotherapy Protocols; Bone Marrow Trans

1992
Cancrum oris-like lesions.
    The British journal of oral & maxillofacial surgery, 1991, Volume: 29, Issue:1

    Topics: Ampicillin; Busulfan; Candida albicans; Chronic Disease; Diagnosis, Differential; Disease Susceptibi

1991
Autografting for patients with chronic myeloid leukaemia in chronic phase: peripheral blood stem cells may have a finite capacity for maintaining haemopoiesis.
    British journal of haematology, 1989, Volume: 73, Issue:1

    Topics: Adult; Antineoplastic Combined Chemotherapy Protocols; Busulfan; Chronic Disease; Combined Modality

1989
Remission of chronic idiopathic myelofibrosis to busulphan treatment.
    The American journal of the medical sciences, 1989, Volume: 297, Issue:2

    Topics: Busulfan; Chronic Disease; Humans; Primary Myelofibrosis

1989
Busulfan-induced sideroblastic anemia.
    American journal of hematology, 1988, Volume: 28, Issue:3

    Topics: Anemia, Sideroblastic; Bone Marrow; Busulfan; Chronic Disease; Cytarabine; Drug Therapy, Combination

1988
Remission of chronic idiopathic myelofibrosis to busulfan treatment.
    The American journal of the medical sciences, 1988, Volume: 295, Issue:5

    Topics: Aged; Biopsy; Bone Marrow; Busulfan; Chronic Disease; Drug Evaluation; Female; Humans; Male; Middle

1988
[Development of polycythemia vera during chronic idiopathic myelofibrosis].
    Minerva medica, 1985, Dec-22, Volume: 76, Issue:49-50

    Topics: Adult; Anemia, Myelophthisic; Busulfan; Chronic Disease; Hepatomegaly; Humans; Male; Platelet Count;

1985
Chronic granulomatous disease: quantitative clinicopathological relationships.
    Archives of disease in childhood, 1970, Volume: 45, Issue:239

    Topics: Adolescent; Anemia; Arthritis; Blood Proteins; Body Height; Body Weight; Busulfan; Child; Child, Pre

1970
Hypereosinophilic syndrome. Report of two cases, with prolonged courses.
    The American journal of medicine, 1971, Volume: 51, Issue:4

    Topics: Adult; Busulfan; Cardiomegaly; Chronic Disease; Cyclophosphamide; Eosinophilia; Eosinophils; Hepatom

1971
Chronic granulocytic leukaemia and chronic lymphocytic leukaemia.
    British medical journal, 1974, Nov-23, Volume: 4, Issue:5942

    Topics: Allopurinol; Amenorrhea; Busulfan; Chlorambucil; Chronic Disease; Drug Eruptions; Female; Hemolysis;

1974
[Polycythemia vera].
    Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1974, Nov-20, Volume: 94, Issue:32

    Topics: Busulfan; Chronic Disease; Diagnosis, Differential; Hemorrhage; Humans; Phosphorus Radioisotopes; Po

1974
[Myleran lung in chronic myelosis].
    Wiener Zeitschrift fur innere Medizin und ihre Grenzgebiete, 1973, Volume: 54, Issue:4

    Topics: Busulfan; Carcinoma; Chronic Disease; Diagnosis, Differential; Female; Humans; Leukemia, Myeloid; Lu

1973
Chronic granulocytic leukaemia.
    The Medical journal of Australia, 1974, Jul-06, Volume: 2, Issue:1

    Topics: Adult; Busulfan; Child; Chromosome Aberrations; Chromosomes, Human, 21-22 and Y; Chronic Disease; Di

1974
Neutrophil function in chronic granulocytic leukaemia before and after busulphan treatment.
    British journal of haematology, 1974, Volume: 28, Issue:4

    Topics: Busulfan; Chronic Disease; Humans; Leukemia, Myeloid; Muramidase; Neutrophils; Phagocytosis; Skin Wi

1974
[Antimetabolites and pregnancy. Normal child born to a mother under treatment 8 years for chronic myeloid leukemia].
    Bulletin de l'Academie nationale de medecine, 1972, Feb-01, Volume: 156, Issue:4

    Topics: Abortion, Therapeutic; Adolescent; Busulfan; Chronic Disease; Female; Humans; Leukemia, Myeloid; Leu

1972
Immunosuppressive agents in the treatment of chronic idiopathic thrombocytopenic purpura.
    Paediatrica Indonesiana, 1973, Volume: 13, Issue:3

    Topics: Antibodies; Azathioprine; Blood Platelets; Busulfan; Child; Child, Preschool; Chronic Disease; Drug

1973
Mitomycin C in the treatment of chronic myelogenous leukemia.
    Nagoya journal of medical science, 1967, Volume: 29, Issue:4

    Topics: Animals; Busulfan; Chronic Disease; Leukemia, Myeloid; Mercaptopurine; Mitomycins; Rats

1967
Cytogenetic remission in acute transformation of chronic granulocytic leukaemia.
    British medical journal, 1969, May-31, Volume: 2, Issue:5656

    Topics: Acute Disease; Aged; Aneuploidy; Bone Marrow Diseases; Busulfan; Cell Transformation, Neoplastic; Ch

1969
Blastic crisis of chronic myelogenous leukaemia.
    Neoplasma, 1969, Volume: 16, Issue:4

    Topics: Acute Disease; Adult; Antineoplastic Agents; Busulfan; Chronic Disease; Female; Hematopoiesis; Human

1969
[Chronic myelogenous leukemia. Results of therapy with busulfan].
    Nordisk medicin, 1969, Oct-09, Volume: 82, Issue:41

    Topics: Adult; Age Factors; Aged; Ambulatory Care; Blood Transfusion; Busulfan; Chronic Disease; Female; Fol

1969
[Chronic myelosis. Clinical picture and therapy].
    Wiener Zeitschrift fur innere Medizin und ihre Grenzgebiete, 1969, Volume: 50, Issue:6

    Topics: Antineoplastic Agents; Busulfan; Chronic Disease; Gold Isotopes; Leukemia, Myeloid; Pipobroman; Sple

1969
[Lung changes under busulfan therapy in a case of chronic myelosis].
    Zentralblatt fur allgemeine Pathologie u. pathologische Anatomie, 1970, Volume: 113, Issue:5

    Topics: Busulfan; Chronic Disease; Female; Humans; Leukocyte Count; Lung; Lung Diseases; Middle Aged; Primar

1970
Chronic granulomatous disease of childhood.
    Transactions of the Medical Society of London, 1970, Volume: 86

    Topics: Anti-Bacterial Agents; Busulfan; Child; Child, Preschool; Chronic Disease; Coloring Agents; Female;

1970
Thrombocytosis in chronic inflammatory bowel disease.
    Annals of internal medicine, 1968, Volume: 68, Issue:5

    Topics: Adolescent; Adult; Blood Cell Count; Blood Platelets; Bone Marrow Cells; Busulfan; Chronic Disease;

1968