Page last updated: 2024-11-06

prednisolone and Minimal Disease, Residual

prednisolone has been researched along with Minimal Disease, Residual in 20 studies

Prednisolone: A glucocorticoid with the general properties of the corticosteroids. It is the drug of choice for all conditions in which routine systemic corticosteroid therapy is indicated, except adrenal deficiency states.
prednisolone : A glucocorticoid that is prednisone in which the oxo group at position 11 has been reduced to the corresponding beta-hydroxy group. It is a drug metabolite of prednisone.

Research Excerpts

ExcerptRelevanceReference
"Availability of measurement of minimal residual disease (MRD) at an early time point with a reduced-cost method is of clinical relevance."2.74Risk of relapse of childhood acute lymphoblastic leukemia is predicted by flow cytometric measurement of residual disease on day 15 bone marrow. ( Arico, M; Basso, G; Benetello, A; Biondi, A; Buldini, B; Conter, V; Dworzak, MN; Gaipa, G; Maglia, O; Masera, G; Ratei, R; Silvestri, D; Valsecchi, MG; Veltroni, M, 2009)
"In children with acute lymphoblastic leukemia (ALL), the level of minimal residual disease (MRD) at the end of induction strongly predicts outcome, presumably because it measures both drug sensitivity and the number of leukemic cells requiring elimination."2.68Relationship between minimal residual disease and outcome in adult acute lymphoblastic leukemia. ( Bradstock, K; Brisco, J; Enno, A; Hughes, E; McCaul, K; Morley, AA; Neoh, SH; Sykes, PJ; Szer, J, 1996)
"Even though acute lymphoblastic leukemia (ALL) responds well to chemotherapy, relapse remains the major problem."2.41Low relapse rate in children with acute lymphoblastic leukemia after risk-directed therapy. ( Botsonis, A; Moschovi, M; Papadopoulou, AL; Tsangaris, GT; Tzortzatou-Stathopoulou, F, 2001)
"acute lymphoblastic leukemia-type chemotherapy that incorporated high-dose cytarabine was effective in achieving an minimal residual disease-negativity rate of 69% in evaluated patients, which was also predictive of better outcome."1.56Clinicoepidemiologic Profile and Outcome Predicted by Minimal Residual Disease in Children With Mixed-phenotype Acute Leukemia Treated on a Modified MCP-841 Protocol at a Tertiary Cancer Institute in India. ( Banavali, S; Gujral, S; Myint, HH; Narula, G; Patkar, N; Prasad, M; Subramanian, P; Tandon, S; Tembhare, P, 2020)
"Multivariate analysis revealed that minimal residual disease positive and time interval between induction IA and Protocol M of more than 70 days were independent adverse factors for EFS and OS."1.51Long-term outcomes of modified BFM-95 regimen in adults with newly diagnosed standard-risk acute lymphoblastic leukemia: a retrospective single-center study. ( Cai, X; Chen, X; Li, C; Liang, Y; Wang, H; Xia, Z, 2019)
"The ratio of minimal residual disease was 0."1.38[Detection and impact of minimal residual disease on outcome of chronic lymphocytic leukemia]. ( Bozsó, T; Iványi, JL; Plander, M; Skrapits, J; Szendrei, T, 2012)
"t(12;21)(p1 3;q22), the most frequent chromosomal translocation found in childhood acute lymphoblastic leukemia (ALL), occurs in approximately 25% of B-lineage ALL cases and has been claimed to carry a good prognosis."1.32Post-induction residual disease in translocation t(12;21)-positive childhood ALL. ( Clausen, N; Jonmundsson, GK; Madsen, HO; Nyvold, C; Ryder, LP; Schmiegelow, K; Seyfarth, J; Wesenberg, F, 2003)
"Most prognostic factors in childhood acute lymphoblastic leukemia (ALL) are informative for groups of patients, whereas new approaches are needed to predict the efficacy of chemotherapy for the individual patient."1.31Post-induction residual leukemia in childhood acute lymphoblastic leukemia quantified by PCR correlates with in vitro prednisolone resistance. ( Kaspers, GJ; Knabe, N; Madsen, HO; Nyvold, C; Pieters, R; Rottier, MM; Ryder, LP; Schmiegelow, K; Seyfarth, J; Svejgaard, A, 2001)
"However, minimal residual disease (MRD) detected with DEK/CAN chimeric m-RNA by reverse transcription polymerase chain reaction (RT-PCR) was continuously observed, although decreased quantitatively, following several courses of consolidation and intensification chemotherapies."1.30[The detection of minimal residual disease by DEK/CAN chimeric m-RNA in a case of AML M2 with translocation t(6;9) (p23;q34) after chemotherapy and peripheral blood stem cell transplantation]. ( Ando, T; Ariyoshi, K; Hikiji, K; Kobayashi, M; Shinohara, K; Toyosawa, M, 1997)

Research

Studies (20)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (10.00)18.2507
2000's7 (35.00)29.6817
2010's10 (50.00)24.3611
2020's1 (5.00)2.80

Authors

AuthorsStudies
Myint, HH1
Tandon, S1
Narula, G1
Prasad, M1
Subramanian, P1
Patkar, N1
Tembhare, P1
Gujral, S1
Banavali, S1
Li, C1
Cai, X1
Chen, X1
Liang, Y1
Xia, Z1
Wang, H1
Mei, YY1
Gao, C1
Cui, L1
Zhao, XX1
Zhao, W1
Li, WJ1
Wang, KL1
Jiang, J1
Zhang, RD1
Xie, J1
Shi, HW1
Wang, B1
Zhang, YH1
Ma, XL1
Zhou, X1
Wu, MY1
Li, ZG1
Koh, K1
Tomizawa, D1
Moriya Saito, A1
Watanabe, T1
Miyamura, T1
Hirayama, M1
Takahashi, Y1
Ogawa, A1
Kato, K1
Sugita, K1
Sato, T1
Deguchi, T1
Hayashi, Y1
Takita, J1
Takeshita, Y1
Tsurusawa, M1
Horibe, K1
Mizutani, S1
Ishii, E1
Kim, DY1
Joo, YD1
Lim, SN1
Kim, SD1
Lee, JH3
Kim, DH1
Kim, K1
Jung, CW1
Kim, I1
Yoon, SS1
Park, S1
Ahn, JS1
Yang, DH1
Lee, JJ1
Lee, HS1
Kim, YS1
Mun, YC1
Kim, H1
Park, JH1
Moon, JH1
Sohn, SK1
Lee, SM1
Lee, WS1
Kim, KH1
Won, JH1
Hyun, MS1
Park, J1
Shin, HJ1
Chung, JS1
Lee, H1
Eom, HS1
Lee, GW1
Cho, YU1
Jang, S1
Park, CJ1
Chi, HS1
Lee, KH1
Campana, D1
Pui, CH1
Lönnerholm, G2
Thörn, I2
Sundström, C2
Frost, BM2
Abrahamsson, J1
Behrendtz, M1
Heldrup, J1
Jacobsson, S1
Li, A1
Olofsson, T1
Porwit, A2
Söderhäll, S2
Larsson, R2
Forestier, E2
Basso, G1
Veltroni, M1
Valsecchi, MG1
Dworzak, MN1
Ratei, R1
Silvestri, D1
Benetello, A1
Buldini, B1
Maglia, O1
Masera, G1
Conter, V1
Arico, M1
Biondi, A1
Gaipa, G1
Flaegstad, T1
Heyman, M1
Jonsson, OG1
Harila-Saari, A1
Madsen, HO3
Schmiegelow, K3
Wesenberg, F2
Vettenranta, K1
Lauten, M1
Möricke, A1
Beier, R1
Zimmermann, M1
Stanulla, M1
Meissner, B1
Odenwald, E1
Attarbaschi, A1
Niemeyer, C1
Niggli, F1
Riehm, H1
Schrappe, M1
Krejci, M1
Doubek, M1
Brychtova, Y1
Stehlikova, O1
Chovancova, J1
Tichy, B1
Francova, HS1
Navratil, M1
Tomiska, M1
Horky, O1
Pospisilova, S1
Mayer, J1
Plander, M1
Skrapits, J1
Bozsó, T1
Szendrei, T1
Iványi, JL1
Styczynski, J1
Piatkowska, M1
Jaworska-Posadzy, A1
Czyzewski, K1
Kubicka, M1
Kolodziej, B1
Kurylo-Rafinska, B1
Debski, R1
Pogorzala, M1
Wysocki, M1
Seyfarth, J2
Nyvold, C2
Ryder, LP2
Clausen, N1
Jonmundsson, GK1
Avilés, A1
Neri, N1
Delgado, S1
Pérez, F1
Nambo, MJ1
Cleto, S1
Talavera, A1
Huerta-Guzmán, J1
Hirt, C1
Schüler, F1
Kiefer, T1
Schwenke, C1
Haas, A1
Niederwieser, D1
Neser, S1
Assmann, M1
Srock, S1
Rohrberg, R1
Dachselt, K1
Leithäuser, M1
Rabkin, CS1
Herold, M1
Dölken, G1
Brisco, J1
Hughes, E1
Neoh, SH1
Sykes, PJ1
Bradstock, K1
Enno, A1
Szer, J1
McCaul, K1
Morley, AA1
Toyosawa, M1
Shinohara, K1
Ariyoshi, K1
Ando, T1
Kobayashi, M1
Hikiji, K1
Pieters, R1
Rottier, MM1
Knabe, N1
Svejgaard, A1
Kaspers, GJ1
Tzortzatou-Stathopoulou, F1
Papadopoulou, AL1
Moschovi, M1
Botsonis, A1
Tsangaris, GT1

Clinical Trials (3)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Tasigna® (Nilotinib) Plus Multi-Agent Chemotherapy for Newly-Diagnosed Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia[NCT00844298]Phase 291 participants (Actual)Interventional2009-01-31Completed
Ponatinib Plus Reduced-intensity Chemotherapy in the First-line Treatment of Adult Patients With Ph-positive Acute Lymphoblastic Leukemia[NCT04554459]Phase 232 participants (Anticipated)Interventional2021-02-16Active, not recruiting
Treatment Protocol for Newky Diagnosed Adult Ph-Chromosome Positive (BCR::ABL1) Acute Lymphoblastic Leukemia (LALPh2022)[NCT06175702]150 participants (Anticipated)Observational2023-12-25Not yet recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Proportion of Patients Achieving Hematologic and Molecular Complete Remission (CR) After Induction Therapy

approximate time: at the recovery of cytopenia (NCT00844298)
Timeframe: 1 month

Interventionpercentage of analyzable subjects (Number)
Nilotinib+mVPD91

Reviews

2 reviews available for prednisolone and Minimal Disease, Residual

ArticleYear
Minimal residual disease-guided therapy in childhood acute lymphoblastic leukemia.
    Blood, 2017, 04-06, Volume: 129, Issue:14

    Topics: Antineoplastic Combined Chemotherapy Protocols; Asparaginase; Child, Preschool; Cyclophosphamide; Da

2017
Low relapse rate in children with acute lymphoblastic leukemia after risk-directed therapy.
    Journal of pediatric hematology/oncology, 2001, Volume: 23, Issue:9

    Topics: Adolescent; Antineoplastic Combined Chemotherapy Protocols; Asparaginase; Bone Marrow; Bone Marrow T

2001

Trials

7 trials available for prednisolone and Minimal Disease, Residual

ArticleYear
Nilotinib combined with multiagent chemotherapy for newly diagnosed Philadelphia-positive acute lymphoblastic leukemia.
    Blood, 2015, Aug-06, Volume: 126, Issue:6

    Topics: Adolescent; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Daunorubicin; Drug Administ

2015
Nilotinib combined with multiagent chemotherapy for newly diagnosed Philadelphia-positive acute lymphoblastic leukemia.
    Blood, 2015, Aug-06, Volume: 126, Issue:6

    Topics: Adolescent; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Daunorubicin; Drug Administ

2015
Nilotinib combined with multiagent chemotherapy for newly diagnosed Philadelphia-positive acute lymphoblastic leukemia.
    Blood, 2015, Aug-06, Volume: 126, Issue:6

    Topics: Adolescent; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Daunorubicin; Drug Administ

2015
Nilotinib combined with multiagent chemotherapy for newly diagnosed Philadelphia-positive acute lymphoblastic leukemia.
    Blood, 2015, Aug-06, Volume: 126, Issue:6

    Topics: Adolescent; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Daunorubicin; Drug Administ

2015
Nilotinib combined with multiagent chemotherapy for newly diagnosed Philadelphia-positive acute lymphoblastic leukemia.
    Blood, 2015, Aug-06, Volume: 126, Issue:6

    Topics: Adolescent; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Daunorubicin; Drug Administ

2015
Nilotinib combined with multiagent chemotherapy for newly diagnosed Philadelphia-positive acute lymphoblastic leukemia.
    Blood, 2015, Aug-06, Volume: 126, Issue:6

    Topics: Adolescent; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Daunorubicin; Drug Administ

2015
Nilotinib combined with multiagent chemotherapy for newly diagnosed Philadelphia-positive acute lymphoblastic leukemia.
    Blood, 2015, Aug-06, Volume: 126, Issue:6

    Topics: Adolescent; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Daunorubicin; Drug Administ

2015
Nilotinib combined with multiagent chemotherapy for newly diagnosed Philadelphia-positive acute lymphoblastic leukemia.
    Blood, 2015, Aug-06, Volume: 126, Issue:6

    Topics: Adolescent; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Daunorubicin; Drug Administ

2015
Nilotinib combined with multiagent chemotherapy for newly diagnosed Philadelphia-positive acute lymphoblastic leukemia.
    Blood, 2015, Aug-06, Volume: 126, Issue:6

    Topics: Adolescent; Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Daunorubicin; Drug Administ

2015
Risk of relapse of childhood acute lymphoblastic leukemia is predicted by flow cytometric measurement of residual disease on day 15 bone marrow.
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2009, Nov-01, Volume: 27, Issue:31

    Topics: Adrenal Cortex Hormones; Antineoplastic Combined Chemotherapy Protocols; Bone Marrow; Dexamethasone;

2009
Prediction of outcome by early bone marrow response in childhood acute lymphoblastic leukemia treated in the ALL-BFM 95 trial: differential effects in precursor B-cell and T-cell leukemia.
    Haematologica, 2012, Volume: 97, Issue:7

    Topics: Antineoplastic Combined Chemotherapy Protocols; Asparaginase; Biomarkers; Bone Marrow; Child; Child,

2012
Fludarabine with cytarabine followed by reduced-intensity conditioning and allogeneic hematopoietic stem cell transplantation in patients with poor-risk chronic lymphocytic leukemia.
    Annals of hematology, 2013, Volume: 92, Issue:2

    Topics: Adult; Alemtuzumab; Antibodies, Monoclonal, Humanized; Antibodies, Monoclonal, Murine-Derived; Antin

2013
Residual disease after chemotherapy in aggressive malignant lymphoma: the role of radiotherapy.
    Medical oncology (Northwood, London, England), 2005, Volume: 22, Issue:4

    Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Cyclophosphamide; Doxorubicin; Female;

2005
Rapid and sustained clearance of circulating lymphoma cells after chemotherapy plus rituximab: clinical significance of quantitative t(14;18) PCR monitoring in advanced stage follicular lymphoma patients.
    British journal of haematology, 2008, Volume: 141, Issue:5

    Topics: Adult; Aged; Antibodies, Monoclonal; Antibodies, Monoclonal, Murine-Derived; Antineoplastic Combined

2008
Relationship between minimal residual disease and outcome in adult acute lymphoblastic leukemia.
    Blood, 1996, Jun-15, Volume: 87, Issue:12

    Topics: Adolescent; Adult; Age Factors; Aged; Antineoplastic Combined Chemotherapy Protocols; Asparaginase;

1996

Other Studies

11 other studies available for prednisolone and Minimal Disease, Residual

ArticleYear
Clinicoepidemiologic Profile and Outcome Predicted by Minimal Residual Disease in Children With Mixed-phenotype Acute Leukemia Treated on a Modified MCP-841 Protocol at a Tertiary Cancer Institute in India.
    Journal of pediatric hematology/oncology, 2020, Volume: 42, Issue:7

    Topics: Acute Disease; Adolescent; Antineoplastic Combined Chemotherapy Protocols; Child; Child, Preschool;

2020
Long-term outcomes of modified BFM-95 regimen in adults with newly diagnosed standard-risk acute lymphoblastic leukemia: a retrospective single-center study.
    International journal of hematology, 2019, Volume: 110, Issue:4

    Topics: Adult; Antineoplastic Combined Chemotherapy Protocols; Asian People; Asparaginase; Cohort Studies; C

2019
[Evaluation of the efficacy of two successive protocols on pediatric acute lymphoblastic leukemia with E2A-PBX1 fusion gene].
    Zhonghua er ke za zhi = Chinese journal of pediatrics, 2013, Volume: 51, Issue:6

    Topics: Adolescent; Antineoplastic Combined Chemotherapy Protocols; Child; Child, Preschool; Daunorubicin; D

2013
Early use of allogeneic hematopoietic stem cell transplantation for infants with MLL gene-rearrangement-positive acute lymphoblastic leukemia.
    Leukemia, 2015, Volume: 29, Issue:2

    Topics: Antineoplastic Agents; Child, Preschool; Disease-Free Survival; Female; Gene Rearrangement; Hematopo

2015
In vitro cellular drug sensitivity at diagnosis is correlated to minimal residual disease at end of induction therapy in childhood acute lymphoblastic leukemia.
    Leukemia research, 2009, Volume: 33, Issue:1

    Topics: Adolescent; Antineoplastic Combined Chemotherapy Protocols; Child; Child, Preschool; Doxorubicin; Hu

2009
In vitro cellular drug resistance adds prognostic information to other known risk-factors in childhood acute lymphoblastic leukemia.
    Leukemia research, 2011, Volume: 35, Issue:4

    Topics: Adolescent; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Bone Marrow Cells

2011
[Detection and impact of minimal residual disease on outcome of chronic lymphocytic leukemia].
    Orvosi hetilap, 2012, Oct-14, Volume: 153, Issue:41

    Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Cyclophosphamide; Disease-Free Survival

2012
Comparison of prognostic value of in vitro drug resistance and bone marrow residual disease on day 15 of therapy in childhood acute lymphoblastic leukemia.
    Anticancer research, 2012, Volume: 32, Issue:12

    Topics: Adolescent; Antineoplastic Agents; Asparaginase; Bone Marrow; Child; Child, Preschool; Daunorubicin;

2012
Post-induction residual disease in translocation t(12;21)-positive childhood ALL.
    Medical and pediatric oncology, 2003, Volume: 40, Issue:2

    Topics: Adolescent; Antineoplastic Combined Chemotherapy Protocols; Child; Child, Preschool; Chromosomes, Hu

2003
[The detection of minimal residual disease by DEK/CAN chimeric m-RNA in a case of AML M2 with translocation t(6;9) (p23;q34) after chemotherapy and peripheral blood stem cell transplantation].
    [Rinsho ketsueki] The Japanese journal of clinical hematology, 1997, Volume: 38, Issue:1

    Topics: Adolescent; Antineoplastic Combined Chemotherapy Protocols; Chromosomes, Human, Pair 6; Chromosomes,

1997
Post-induction residual leukemia in childhood acute lymphoblastic leukemia quantified by PCR correlates with in vitro prednisolone resistance.
    Leukemia, 2001, Volume: 15, Issue:7

    Topics: Adolescent; Child; Child, Preschool; Drug Resistance, Neoplasm; Humans; Infant; Neoplasm, Residual;

2001