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Prognostic impact of number of induction courses to attain complete remission in patients with acute myeloid leukemia transplanted with either a matched sibling or human leucocyte antigen 10/10 or 9/10 unrelated donor: An Acute Leukemia Working Party European Society for Blood and Marrow Transplantation study

医学 危险系数 内科学 单变量分析 人类白细胞抗原 多元分析 诱导化疗 肿瘤科 髓系白血病 置信区间 白血病 移植 兄弟姐妹 比例危险模型 免疫学 化疗 抗原 发展心理学 心理学
作者
Justin Loke,Myriam Labopin,Charles Craddock,Gèrard Socié,Tobias Gedde‐Dahl,Didier Blaise,Édouard Forcade,Urpu Salmenniemi,Anne Huynh,Jurjen Versluis,Ibrahim Yakoub‐Agha,Hélène Labussière‐Wallet,Johan Maertens,Jakob Passweg,Claude-Éric Bulabois,Ludovic Gabellier,Stephan Mielke,Cristina Castilla‐Llorente,Éric Deconinck,Éolia Brissot,Arnon Nagler,Fabio Ciceri,Mohamad Mohty
出处
期刊:Cancer [Wiley]
卷期号:130 (15): 2642-2651
标识
DOI:10.1002/cncr.35308
摘要

Abstract Introduction For the majority of patients with acute myeloid leukemia (AML) an allogeneic stem cell transplant (SCT) in first complete remission (CR) is preferred. However, whether the number of courses required to achieve CR has a prognostic impact is unclear. It is unknown which factors remain important in patients requiring more than one course of induction to attain remission. Methods This Acute Leukaemia Working Party study from the European Society for Blood and Marrow Transplantation identified adults who received an allograft in first CR from either a fully matched sibling or 10/10 or 9/10 human leucocyte antigen (HLA)‐matched unrelated donor (HLA‐A, HLA‐B, HLA‐C, HLA‐DR, or HLA‐DQ). Univariate and multivariate analyses were undertaken to identify the prognostic impact of one or two courses of induction to attain CR. Results A total of 4995 patients were included with 3839 (77%) patients attaining a CR following one course of induction chemotherapy (IND1), and 1116 patients requiring two courses (IND2) to attain CR. IND2 as compared to IND1 was a poor prognostic factor in a univariate analysis and remained so in a multivariate Cox model, resulting in an increased hazard ratio of relapse (1.38; 95% confidence interval [CI], 1.16–1.64; p = .0003) and of death (1.27; 95% CI, 1.09–1.47; p = .002). Adverse prognostic factors in a multivariate analysis of the outcomes of patients requiring IND2 included age, FLT3 ‐ITD, adverse cytogenetics, and performance status. Pretransplant measurable residual disease retained a prognostic impact regardless of IND1 or IND2. Conclusion Initial response to chemotherapy as determined by number of courses to attain CR, retained prognostic relevance even following SCT in CR.

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