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Acute promyelocytic leukemia: long-term outcomes from the HARMONY project

急性早幼粒细胞白血病 内科学 队列 医学 三氧化二砷 养生 随访中值 儿科 总体生存率 维甲酸 生物化学 基因 化学 细胞凋亡
作者
Maria Teresa Voso,Luca Guarnera,Sylvain Lehmann,Konstanze Döhner,Hartmut Döhner,Uwe Platzbecker,Nigel H. Russell,Richard Dillon,Ian Thomas,Gert J. Ossenkoppele,Torsten Haferlach,Marco Vignetti,Edoardo La Sala,Alfonso Piciocchi,Paola Fazi,Ángela Villaverde Ramiro,Laura Tur Giménez,Carmelo Gurnari,Lars Bullinger,Jesús María Hernández‐Rivas
出处
期刊:Blood [American Society of Hematology]
卷期号:145 (2): 234-243 被引量:24
标识
DOI:10.1182/blood.2024026186
摘要

Abstract Treatment outcomes for acute promyelocytic leukemia (APL) have improved with the widespread use of targeted therapy with all-trans retinoic acid (ATRA) and arsenic trioxide (ATO). Our study aimed to validate these data in a large patient cohort, and to redefine prognostic factors. Leveraging the HARMONY Platform, we analyzed 1438 newly diagnosed patients with APL, diagnosed between 1999 and 2022. Patient data derived from the 2 international multicenter Gruppo Italiano Malattie EMatologiche dell’Adulto (GIMEMA)-APL0406 and National Cancer Research Institute (NCRI)-AML17 trials and 4 European registries: the Haemato Oncology Foundation for Adults in the Netherlands, Belgium and Luxembourg (HOVON), AML Study Group (AMLSG), Swedish AML Registry, and Study Alliance Leukemia (SAL). The study cohort included 721 males and 717 females, with a median age of 50.5 years (range, 16-94 years). Of 1309 patients starting therapy, 562 received ATRA-ATO, and 747 idarubicin-based chemotherapy (AIDA-like CHT). Early death (ED) occurred in 85 of 1438 patients (5.9%) at a median of 9 days after APL diagnosis and was independently associated with increasing age and high Sanz risk score (odds ratio [OR], 1.06; 95% confidence interval [CI], 1.04-1.08; and OR, 4.65; 95% CI, 2.55-8.51, respectively). The median follow-up was 5.5 years (interquartile range, 3.2-7.5 years). ATRA-ATO regimen was associated with the best outcome, reaching 91% 7-year overall survival (vs 81% for AIDA-like CHT; hazard ratio [HR], 2.14; 95% CI, 1.51-3.05), 89% event-free survival (vs 71% for AIDA-like CHT; HR, 2.72; 95% CI, 2.01–3.69), and 3% relapse (vs 13% for AIDA-like CHT; HR, 4.19; 95% CI, 2.38-7.39; P < .001 for all outcomes). The survival advantage of ATRA/ATO was independent of patients’ age, Sanz risk score, and treatment scenario. Our study confirms the superiority of ATRA-ATO over ATRA-chemotherapy in patients with APL. Reducing the risk of ED still represents an unmet medical need, in particular in older patients and in high-risk APL.
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