Daunorubicin Versus Mitoxantrone Versus Idarubicin As Induction and Consolidation Chemotherapy for Adults With Acute Myeloid Leukemia: The EORTC and GIMEMA Groups Study AML-10

去甲柔比星 米托蒽醌 医学 柔红霉素 阿糖胞苷 依托泊苷 内科学 髓系白血病 化疗 白血病 外科 诱导化疗 肿瘤科 胃肠病学
作者
Franco Mandelli,Marco Vignetti,Stefan Suciu,Roberto Stasi,M C Petti,Giovanna Meloni,Petra Muus,Filippo Marmont,Jean‐Pierre Marie,Boris Labar,Xavier Thomas,Francesco Di Raimondo,R. Willemze,Vincenzo Liso,Felicetto Ferrara,Liliana Baila,Paola Fazi,R Zittoun,Sergio Amadori,Théo de Witte
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:27 (32): 5397-5403 被引量:175
标识
DOI:10.1200/jco.2008.20.6490
摘要

Purpose To compare the antitumor efficacy of three different anthracyclines in combination with cytarabine and etoposide in adult patients with newly diagnosed acute myeloid leukemia (AML). Patients and Methods We randomly assigned 2,157 patients (age range, 15 to 60 years) to receive intensive induction-consolidation chemotherapy containing either daunorubicin, idarubicin, or mitoxantrone. After achieving complete remission (CR), patients were assigned to undergo either allogeneic or autologous stem-cell transplantation (SCT), depending on the availability of a sibling donor. Results The overall CR rate (69%) was similar in the three groups. Autologous SCT was performed in 37% of cases in the daunorubicin arm versus only 29% and 31% in mitoxantrone and idarubicin, respectively (P < .001). However, the disease-free survival (DFS) and survival from CR were significantly shorter in the daunorubicin arm: the 5-year DFS was 29% versus 37% and 37% in mitoxantrone and idarubicin, respectively. The proportion of patients who underwent allogeneic SCT (22%) was equivalent in the three treatment groups, and the outcome was similar as well: the 5-year overall survival rates were 34%, 34%, and 31%, respectively. Conclusion In adult patients with AML who do not receive an allogeneic SCT, the use of mitoxantrone or idarubicin instead of daunorubicin enhances the long-term efficacy of chemotherapy.
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