Tang Kenny, Lipton Jeffrey H
Division of Medical Oncology and Hematology, University Health Network - Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.
Department of Haematology, Blacktown Hospital, New South Wales, Australia.
Leuk Lymphoma. 2024 Jun;65(6):705-714. doi: 10.1080/10428194.2024.2313626. Epub 2024 Feb 9.
Due to the remarkable success of tyrosine kinase inhibitors (TKI) in chronic myeloid leukemia (CML), allogeneic stem cell transplantation (alloSCT) is not first-line treatment for delivering durable, long-term survival. Consequently, alloSCT is reserved for patients with TKI-resistant or TKI-intolerant chronic phase CML (CP-CML) and advanced phase CML (AP-CML). Advances in transplant technology, such as high-resolution HLA typing, introduction of reduced intensity conditioning and increased alternative donor availability, coupled with improved supportive care, have significantly reduced transplant-related mortality and expanded the pool of transplant-eligible patients. Refinement of conditioning regimens, innovative use of post-transplant cellular and pharmacological therapies, and judicious post-transplant monitoring are important strategies for reducing risk of relapse. Given its potential to cure, alloSCT will invariably remain a key part of the treatment algorithm. This article reviews the data underpinning the role and outcomes of alloSCT and provides an update on current recommendations.
由于酪氨酸激酶抑制剂(TKI)在慢性髓性白血病(CML)治疗中取得了显著成功,异基因干细胞移植(alloSCT)已不再是实现持久长期生存的一线治疗方法。因此,alloSCT 仅适用于对 TKI 耐药或不耐受的慢性期 CML(CP-CML)以及晚期 CML(AP-CML)患者。移植技术的进步,如高分辨率 HLA 分型、降低强度预处理方案的引入以及更多替代供体的可及性,再加上支持治疗的改善,显著降低了移植相关死亡率,并扩大了适合移植患者的范围。优化预处理方案、创新性地使用移植后细胞和药物治疗以及审慎的移植后监测是降低复发风险的重要策略。鉴于其治愈潜力,alloSCT 将始终是治疗方案的关键组成部分。本文回顾了支持 alloSCT 作用和疗效的数据,并提供了当前推荐的最新信息。