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前瞻性分析急性白血病患者异基因造血细胞移植的障碍。

Prospective analysis to determine barriers to allogeneic hematopoietic cell transplantation in patients with acute leukemia.

机构信息

Cellular Therapy Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

出版信息

Am J Hematol. 2023 Dec;98(12):1869-1876. doi: 10.1002/ajh.27084. Epub 2023 Sep 9.

Abstract

Allogeneic hematopoietic cell transplantation (allo-HCT) is a potentially curative treatment for patients with acute leukemia. Despite this, studies have shown that only a minority of patients ultimately proceed to allo-HCT. The primary objective of this prospective, observational study was to identify the rate of allo-HCT in patients for whom it was recommended, and reasons why patients deemed appropriate and eligible for HCT did not subsequently undergo transplant. Between April 2016 and April 2021, adult patients with newly diagnosed or relapsed/refractory acute leukemia were enrolled at the time of induction/reinduction therapy. Initial transplantation workup and allo-HCT recommendations were made during the early phase of induction/reinduction. Of the 307 enrolled patients, allo-HCT was recommended to 85% (n = 259), of whom 66% (n = 170) underwent transplant. Donor sources comprised 54% human leukocyte antigen (HLA)-matched unrelated donors, 20% HLA-matched sibling donors and HLA-mismatched graft sources with 15% umbilical cord blood units, 8% HLA-mismatched unrelated donors, and 4% HLA-haploidentical donors. The most common reason for transplant disqualification in the 89 patients in whom it was initially recommended was persistent/relapsed disease (70%), followed by early patient death (10%). In this prospective study, we report a high allo-HCT rate, which may be due to early transplant referral and workup. The main allo-HCT barrier was disease control, followed by early patient death. With the increasing availability of HLA-mismatched graft sources, the lack of donor availability was not a transplant barrier. Further development of novel transplant strategies for patients not achieving remission and improvements in induction regimens could result in increased allo-HCT utilization.

摘要

异基因造血细胞移植(allo-HCT)是治疗急性白血病患者的一种潜在治愈方法。尽管如此,研究表明,只有少数患者最终接受 allo-HCT。这项前瞻性、观察性研究的主要目的是确定建议进行 allo-HCT 的患者的 allo-HCT 率,以及为什么被认为适合和有资格接受 HCT 的患者最终没有进行移植的原因。在 2016 年 4 月至 2021 年 4 月期间,在诱导/再诱导治疗时纳入了新诊断或复发/难治性急性白血病的成年患者。在诱导/再诱导的早期阶段进行了初始移植评估和 allo-HCT 建议。在 307 名入组患者中,85%(n=259)建议进行 allo-HCT,其中 66%(n=170)接受了移植。供体来源包括 54%的人类白细胞抗原(HLA)匹配的无关供体、20%的 HLA 匹配的同胞供体和 HLA 不匹配的移植物来源,其中包括 15%的脐带血单位、8%的 HLA 不匹配的无关供体和 4%的 HLA 半相合供体。在最初建议进行移植的 89 名患者中,移植不合格的最常见原因是疾病持续存在/复发(70%),其次是患者早期死亡(10%)。在这项前瞻性研究中,我们报告了高 allo-HCT 率,这可能是由于早期的移植转诊和评估。主要的 allo-HCT 障碍是疾病控制,其次是患者早期死亡。随着 HLA 不匹配移植物来源的可用性增加,供体缺乏不是移植障碍。为未达到缓解的患者开发新的移植策略以及改进诱导方案可能会导致 allo-HCT 的利用率增加。

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本文引用的文献

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