The treatment of Philadelphia chromosome-positive B-cell acute lymphoblastic leukemia (Ph+ B-cell ALL) has seen substantial progress over the past two decades. The introduction ofBCR::ABL1tyrosine kinase inhibitor (TKIs) has resulted in dramatic improvements in long-term survival. Allogeneic hematopoietic stem cell transplantation (allo-HSCT), with its curative potential, has always been an integral part of the treatment algorithm of Ph+ ALL. Recently, the approval of novel therapies such as blinatumomab, inotuzumab ozogamicin and chimeric antigen receptor T-cell (CAR-T) therapy in relapse and refractory (R/R) ALL have further improved outcomes of B-cell ALL. With potent TKIs and novel targeted therapy, the treatment guidelines for Ph+ ALL are evolving rapidly. Additionally, with improved tools for detecting measurable residual disease (MRD), there has been recent interest in redefining the role of allo-HSCT for some patients. In this context, we discuss the current evidence for the utilization of allo-HSCT for Ph+ ALL, focusing on novel therapies and MRD-directed care.
费城染色体阳性B细胞急性淋巴细胞白血病(Ph+ B细胞ALL)的治疗在过去二十年中取得了显著进展。BCR::ABL1酪氨酸激酶抑制剂(TKIs)的应用显著改善了患者的长期生存率。异基因造血干细胞移植(allo-HSCT)因其治愈潜力,一直是Ph+ ALL治疗方案中不可或缺的一部分。近年来,针对复发难治性(R/R)ALL的新型疗法,如贝林妥欧单抗、奥加伊妥珠单抗以及嵌合抗原受体T细胞(CAR-T)疗法的获批,进一步改善了B细胞ALL的治疗效果。随着强效TKIs和新型靶向疗法的应用,Ph+ ALL的治疗指南正在迅速演变。此外,随着可测量残留病(MRD)检测工具的改进,近期学界开始重新评估allo-HSCT在某些患者中的作用。在此背景下,本文探讨了当前allo-HSCT在Ph+ ALL治疗中的应用证据,重点关注新型疗法和基于MRD指导的治疗策略。