Department of Internal Medicine V, University Hospital of Heidelberg, Heidelberg, Germany.
Clinical Cooperation Unit Molecular Hematology/Oncology, German Cancer Research Center (DKFZ) and Department of Internal Medicine V, University Hospital of Heidelberg, Heidelberg, Germany.
Leukemia. 2018 Jun;32(6):1277-1294. doi: 10.1038/s41375-018-0139-4. Epub 2018 Apr 24.
With the introduction of all-trans retinoic acid (ATRA) and arsenic trioxide (ATO) acute promyelocytic leukemia (APL) has become from a detrimental to one of the most curable malignant diseases in humans. In particular, the chemotherapy-free regimen with ATO/ATRA has been proven to be highly effective in de novo APL and has become standard first-line therapy in younger adult, non-high-risk patients. Nevertheless, early death is still a major issue in APL, particularly in older patients, emphasizing the need of rapid diagnostics and supportive care together with immediate access to ATRA-based therapy. Despite the dramatic progress achieved in therapy of APL challenging situations occur, particularly in patients excluded from controlled studies with clinical knowledge mainly based on case reports and registries. Rapid identification and treatment of newly diagnosed patients as well as the management of toxicities and complications remain challenging. We offer up-to-date information and guidance regarding treatment of APL. Based on a literature review of existing scientific evidence we also discuss the approach to high-risk, elderly, pregnant and pediatric patients, treatment in patients with renal failure as well as of therapy-related or relapsed/refractory APL.
随着全反式维甲酸(ATRA)和三氧化二砷(ATO)的引入,急性早幼粒细胞白血病(APL)已从一种致命疾病转变为人类最可治愈的恶性疾病之一。特别是,ATO/ATRA 无化疗方案已被证明对初发 APL 非常有效,已成为年轻成人、非高危患者的标准一线治疗。然而,早期死亡仍然是 APL 的一个主要问题,特别是在老年患者中,这强调了需要快速诊断和支持性护理,以及立即获得基于 ATRA 的治疗。尽管在 APL 的治疗方面取得了显著进展,但仍存在具有挑战性的情况,特别是在排除在具有主要基于病例报告和登记的临床知识的对照研究之外的患者中。快速识别和治疗新诊断的患者以及管理毒性和并发症仍然具有挑战性。我们提供有关 APL 治疗的最新信息和指导。基于对现有科学证据的文献回顾,我们还讨论了高危、老年、妊娠和儿科患者的治疗方法,以及肾功能衰竭患者的治疗方法以及与治疗相关或复发/难治性 APL 的治疗方法。