Clinical perspectives on post-induction maintenance therapy in patients with acute myeloid leukaemia in remission who are ineligible for allogeneic haematopoietic stem cell transplantation

IF 5.1 2区 医学 Q1 HEMATOLOGY British Journal of Haematology Pub Date : 2024-12-02 DOI:10.1111/bjh.19924
Kendra Sweet, Thomas Cluzeau
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Abstract

For patients with acute myeloid leukaemia (AML) who achieve complete remission (CR) after induction therapy, subsequent allogeneic haematopoietic stem cell transplantation (allo-HSCT) reduces the risk of relapse. However, not all patients are eligible, warranting effective alternative maintenance strategies. Oral azacitidine is the only non-targeted therapy approved by both the United States (US) Food and Drug Administration and the European Medicines Agency for the maintenance or continued treatment of allo-HSCT-ineligible patients with AML achieving CR or CR with incomplete haematological recovery following induction chemotherapy. Midostaurin and histamine dihydrochloride are approved in Europe as maintenance therapy for AML in remission, and quizartinib is approved in the United States and Europe for the treatment and maintenance of patients with newly diagnosed FLT3-ITD AML. Barriers to maintenance treatment include limited clinical trial data informing appropriate patient and treatment selection, patient preference, financial burden and paucity of real-world data. This article discusses current maintenance treatment guidelines for patients with AML in remission but not proceeding to allo-HSCT and reviews clinical trial data for agents approved for use in remission. Ongoing studies of interest and considerations for future efforts are also discussed.

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不适合异体造血干细胞移植的急性髓系白血病缓解期患者诱导后维持治疗的临床前景
对于在诱导治疗后达到完全缓解(CR)的急性髓性白血病(AML)患者,后续的同种异体造血干细胞移植(alloo - hsct)可降低复发风险。然而,并非所有患者都符合条件,因此需要有效的替代维持策略。口服阿扎胞苷是美国食品和药物管理局(fda)和欧洲药品管理局(ema)批准的唯一一种非靶向治疗,用于维持或继续治疗诱导化疗后达到CR或CR且血液学恢复不完全的AML患者。midoin和盐酸组胺在欧洲被批准作为缓解期AML的维持治疗,quizartinib在美国和欧洲被批准用于新诊断的FLT3-ITD AML患者的治疗和维持。维持治疗的障碍包括告知适当患者和治疗选择的临床试验数据有限、患者偏好、经济负担和缺乏真实世界数据。本文讨论了目前急性髓系白血病缓解期患者的维持治疗指南,但不进行同种异体造血干细胞移植,并回顾了批准用于缓解期药物的临床试验数据。还讨论了正在进行的感兴趣的研究和对未来努力的考虑。
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来源期刊
CiteScore
8.60
自引率
4.60%
发文量
565
审稿时长
1 months
期刊介绍: The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.
期刊最新文献
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