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费城染色体阳性急性淋巴细胞白血病患者的异基因移植:在酪氨酸激酶抑制剂时代是否必不可少?

Allogeneic transplantation for patients with Philadelphia chromosome positive acute lymphoblastic leukemia: Is it imperative in the tyrosine kinase inhibitor era?

作者信息

Litzow Mark R

机构信息

Division of Hematology and Blood and Marrow Transplant, Mayo Clinic, 200 1st Street South West, Rochester, MN 55905, USA.

出版信息

Best Pract Res Clin Haematol. 2018 Dec;31(4):357-360. doi: 10.1016/j.beha.2018.09.004. Epub 2018 Sep 20.

DOI:10.1016/j.beha.2018.09.004
PMID:30466747
Abstract

Before the advent of tyrosine kinase inhibitors (TKIs), Philadelphia chromosome positive acute lymphoblastic leukemia (Ph+ ALL) was associated with dismal survival without allogeneic hematopoietic stem cell transplantation (allo-HSCT). Recent evidence has demonstrated that the combination of TKI and chemotherapy can result in a high rate of complete remission, thereby enabling more patients to proceed to allo-HSCT. However, with more studies reporting non-inferior outcomes with TKI and chemotherapy combination without allo-HSCT, the need for allo-HSCT in Ph+ ALL has become less certain. This review summarizes evidence that will address the relevance of allo-HSCT in Ph+ ALL.

摘要

在酪氨酸激酶抑制剂(TKIs)出现之前,费城染色体阳性急性淋巴细胞白血病(Ph+ ALL)患者若不进行异基因造血干细胞移植(allo-HSCT),其生存率极低。最近的证据表明,TKI与化疗联合应用可导致高完全缓解率,从而使更多患者能够进行allo-HSCT。然而,随着越来越多的研究报告称,TKI与化疗联合应用且不进行allo-HSCT也能取得非劣效的结果,Ph+ ALL患者进行allo-HSCT的必要性变得不那么确定了。本综述总结了相关证据,以探讨allo-HSCT在Ph+ ALL中的相关性。

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