PD-1 inhibitor in patients with minimal residual disease who failed donor lymphocyte infusion or interferon after allogeneic haematopoietic stem cell transplantation

PD-1抑制剂用于异基因造血干细胞移植后供体淋巴细胞输注或干扰素治疗失败的微小残留病灶患者

阅读:1

Abstract

This study aimed to evaluate the efficacy and safety of programmed death receptor 1 (PD-1) antibody in patients with acute myeloid leukaemia (AML) or myelodysplastic syndrome (MDS) with minimal residual disease (MRD) after allogeneic haematopoietic stem cell transplantation (allo-HSCT). Six patients were retrospectively reviewed in this study, and all had failed prior treatment (donor lymphocyte infusion or interferon) before PD-1 antibody administration. Among these 6 patients, two received PD-1 alone while four received PD-1 plus azacitidine. The median treatment with the PD-1 antibody was four doses (range, 1-7 doses). Three patients developed > grade 3 toxicity, including 2 deaths. Among the five evaluable patients, four achieved negative MRD with a median time to response of 2 months (range: 1-3 months); and the median duration of response was 105 days (range: 26-211 days). The median survival time of the five patients was 320 days (range: 107-350 days). Our data suggest that anti-PD-1 antibody in AML/MDS patients with positive MRD following allo-HSCT may be a treatment option.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。