Literature DB >> 10475617

A phase III comparison of high dose ARA-C (HIDAC) versus HIDAC plus mitoxantrone in the treatment of first relapsed or refractory acute myeloid leukemia Southwest Oncology Group Study.

C Karanes1, K J Kopecky, D R Head, M R Grever, H E Hynes, E H Kraut, R H Vial, A Lichtin, S Nand, W E Samlowski, F R Appelbaum.   

Abstract

The aim of this study is to determine whether the addition of mitoxantrone to high dose cytarabine improves the outcome of treatment in patients with relapsed or refractory acute myeloid leukemia (AML). One hundred and sixty-two eligible patients, 14-76 years of age, with AML either in first relapse or that failed to respond to initial remission induction therapy, with no CNS involvement were randomized to receive therapy with cytarabine 3 gm/M2 i.v. over 2 h every 12 h for 12 doses on days 1-6 (Arm I) (HIDAC); or HIDAC plus mitoxantrone 10 mg/M2 i.v. daily on days 7 9 (Arm II) (HIDAC + M). Patients achieving complete remission were treated with three courses of consolidation including HIDAC (Ara-C 3 gm/M2 i.v. 12 h days 1 3; 2 gm/M2 over age 50) alone (ARM I) or with mitoxantrone (10 mg/M2 i.v. day 1) (ARM II). Among 162 patients (81 HIDAC, 81 HIDAC + M) evaluated for induction toxicity, there were 10 (12%) induction deaths with HIDAC and 13 (17%) with HIDAC + M (2-tailed P = 0.65). Most early deaths were due to infection and/or hemorrhage. Among 162 patients evaluated for responses to induction therapy, 26/81 (32%) HIDAC and 36/81 (44%) HIDAC + M patients achieved complete remission (two-tailed P = 0.15). Although this difference was not statistically significant in univariate analysis, it was after adjusting for the effects of WBC and PMN percentage in multivariate analysis (P=0.013). Median survivals from study entry were 8 months (HIDAC) and 6 months (HIDAC + M); 2-tailed logrank P = 0.58. Among 48 patients registered for consolidation, the median disease-free survivals from that registration were 8 months with HIDAC and 11 months with HIDAC + M (P = 0.60). There were three treatment-related deaths during consolidation (1 HIDAC, 2 HIDAC + M), all due to infections. In this randomized trial, the addition of mitoxantrone to high-dose cytarabine was associated with a trend toward a higher CR rate. There was less evidence for an advantage in disease-free or overall survival, although any such conclusion is limited by the size of the study.

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Year:  1999        PMID: 10475617     DOI: 10.1016/s0145-2126(99)00087-9

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


  20 in total

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4.  A phase 1 study of azacitidine with high-dose cytarabine and mitoxantrone in high-risk acute myeloid leukemia.

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Journal:  Blood Adv       Date:  2020-02-25

5.  High dose cytarabine, mitoxantrone and l-asparaginase (HAMA) salvage for relapsed or refractory acute myeloid leukemia (AML) in the elderly.

Authors:  Tamjeed Ahmed; Scott Holwerda; Heidi D Klepin; Scott Isom; Leslie R Ellis; Susan Lyerly; Megan Manuel; Sarah Dralle; Dmitriy Berenzon; Bayard L Powell; Timothy S Pardee
Journal:  Leuk Res       Date:  2015-06-01       Impact factor: 3.156

Review 6.  Acute myeloid leukemia in adults.

Authors:  L D Cripe; S Hinton
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7.  How I treat relapsed or refractory AML.

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8.  Clofarabine plus cytarabine compared with cytarabine alone in older patients with relapsed or refractory acute myelogenous leukemia: results from the CLASSIC I Trial.

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Journal:  J Clin Oncol       Date:  2012-05-14       Impact factor: 44.544

9.  Randomized phase II trial of cytosine arabinoside with and without the CHK1 inhibitor MK-8776 in relapsed and refractory acute myeloid leukemia.

Authors:  Jonathan A Webster; Raoul Tibes; Larry Morris; Amanda L Blackford; Mark Litzow; Mrinal Patnaik; Gary L Rosner; Ivana Gojo; Robert Kinders; Lihua Wang; L Austin Doyle; Catherine J Huntoon; Larry M Karnitz; Scott H Kaufmann; Judith E Karp; B Douglas Smith
Journal:  Leuk Res       Date:  2017-09-20       Impact factor: 3.715

10.  Molecular remission and response patterns in patients with mutant-IDH2 acute myeloid leukemia treated with enasidenib.

Authors:  Eytan M Stein; Courtney D DiNardo; Amir T Fathi; Daniel A Pollyea; Richard M Stone; Jessica K Altman; Gail J Roboz; Manish R Patel; Robert Collins; Ian W Flinn; Mikkael A Sekeres; Anthony S Stein; Hagop M Kantarjian; Ross L Levine; Paresh Vyas; Kyle J MacBeth; Alessandra Tosolini; Jason VanOostendorp; Qiang Xu; Ira Gupta; Thomas Lila; Alberto Risueno; Katharine E Yen; Bin Wu; Eyal C Attar; Martin S Tallman; Stéphane de Botton
Journal:  Blood       Date:  2018-12-03       Impact factor: 25.476

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