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成人急性淋巴细胞白血病的造血干细胞移植:现状。

Hematopoietic stem cell transplant in adults with acute lymphoblastic leukemia: the present state.

机构信息

a Division of Hematology and Bone Marrow Transplant , Mayo Clinic , Rochester , MN , USA.

出版信息

Expert Rev Hematol. 2018 Mar;11(3):195-207. doi: 10.1080/17474086.2018.1433030. Epub 2018 Feb 7.

Abstract

Allogeneic hematopoietic stem cell transplant (allo-HSCT) has an important role in management of acute lymphoblastic leukemia (ALL). Proper patient selection is central to ensure optimal outcomes. Areas covered: This review covers various aspects of HSCT in ALL patients, including indications, donor selection, conditioning regimens, and post-transplant management. Expert commentary: Allo-HSCT is important in post-remission management of ALL but proper risk-stratification is a major challenge. Incorporation of minimal residual disease (MRD) and molecular testing will improve patient allocation. Patients receiving pediatric-inspired induction who achieve molecular remission might not need allo-HSCT in first remission. Allo-HSCT should be considered in patients who don't achieve MDR negativity, didn't receive intensive induction, or have high risk cytogenetic and molecular features. Despite improved responses with tyrosine kinase inhibitors (TKIs) in Philadelphia positive (Ph+) ALL, allo-HSCT remains standard. Matched sibling donors are the optimal graft source, but other sources are valid alternatives. There is no single optimal conditioning regimen and retrospective studies found myeloablative and reduced intensity regimens to be comparable. Following allo-HSCT, there is no role for maintenance therapy in Philadelphia-negative ALL. In Ph+ ALL, maintenance TKIs improve outcomes. The integration of targeted and immunotherapies in the peri-transplant period holds potential for improved outcomes.

摘要

异基因造血干细胞移植(allo-HSCT)在急性淋巴细胞白血病(ALL)的治疗中具有重要作用。适当的患者选择是确保最佳疗效的关键。

涵盖领域

本篇综述涵盖了 ALL 患者 HSCT 的各个方面,包括适应证、供者选择、预处理方案和移植后管理。

专家评论

allo-HSCT 在 ALL 缓解后的治疗中很重要,但适当的风险分层是一个主要挑战。将微小残留病(MRD)和分子检测纳入其中将改善患者的分配。接受儿科诱导方案且达到分子缓解的患者可能在首次缓解期不需要 allo-HSCT。对于未达到 MDR 阴性、未接受强化诱导或具有高风险细胞遗传学和分子特征的患者,应考虑 allo-HSCT。尽管酪氨酸激酶抑制剂(TKI)在费城阳性(Ph+)ALL 中的应用提高了缓解率,但 allo-HSCT 仍然是标准治疗。同胞供者是最佳的移植物来源,但其他来源也是有效的替代选择。没有单一的最佳预处理方案,回顾性研究发现清髓性和减低强度预处理方案的疗效相当。allo-HSCT 后,费城阴性 ALL 无需维持治疗。在 Ph+ ALL 中,维持 TKI 可改善预后。在移植期应用靶向和免疫治疗可能会提高疗效。

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