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造血干细胞移植治疗成人急性淋巴细胞白血病:美国移植和细胞治疗学会 2019 年更新的循证综述。

Hematopoietic Cell Transplantation in the Treatment of Adult Acute Lymphoblastic Leukemia: Updated 2019 Evidence-Based Review from the American Society for Transplantation and Cellular Therapy.

机构信息

Blood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA.

Department of Medical Oncology & Hematology, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH.

出版信息

Biol Blood Marrow Transplant. 2019 Nov;25(11):2113-2123. doi: 10.1016/j.bbmt.2019.08.014. Epub 2019 Aug 22.

Abstract

The role of hematopoietic cell transplantation (HCT) in adults with acute lymphoblastic leukemia (ALL) is reviewed and critically evaluated in this systematic evidence-based review. Specific criteria were used for searching the published literature and for grading the quality and strength of the evidence and the strength of the recommendations. A panel of ALL experts developed consensus on the treatment recommendations based on the evidence. Allogeneic HCT offers a survival benefit in selected patients with ALL, and this review summarizes the standard indications as well as the areas of controversy. There is now greater experience with pediatric-inspired chemotherapy regimens that has transformed upfront therapy for adult ALL, resulting in higher remission rates and overall survival. This in turn has increased the equipoise around decision making for ALL in first complete remission (CR1) when there is no measurable residual disease (MRD) at the end of induction and/or consolidation. Randomized studies are needed for adults with ALL to compare allogeneic HCT in CR1 with pediatric-inspired chemotherapy alone. Indications for transplantation in the evolving landscape of MRD assessments and novel targeted and immune therapeutics remain important areas of investigation.

摘要

在这个系统的循证综述中,回顾并批判性地评估了造血细胞移植(HCT)在成人急性淋巴细胞白血病(ALL)中的作用。为了搜索已发表的文献以及评估证据的质量和强度以及建议的强度,使用了特定的标准。ALL 专家组根据证据就治疗建议达成了共识。异基因 HCT 为特定 ALL 患者提供生存获益,本综述总结了标准适应证以及有争议的领域。现在,儿童启发的化疗方案的经验越来越多,这改变了成人 ALL 的初始治疗方法,导致缓解率和总生存率提高。这反过来又增加了在诱导和/或巩固治疗结束时无可测量残留疾病(MRD)时,在第一个完全缓解(CR1)时对 ALL 进行决策的平衡。需要对 ALL 成人进行随机研究,以比较 CR1 中的异基因 HCT 与单独的儿童启发化疗。在 MRD 评估和新型靶向和免疫治疗的不断发展的背景下,移植的适应证仍然是重要的研究领域。

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