Ma Ling, Li Si-Qi, Han Wei, Fu Hai-Xia, Chen Yao, Ma Rui, Chen Yu-Hong, Zhang Xiao-Hui, Xu Lan-Ping, Wang Yu, Yan Chen-Hua, Wang Feng-Rong, Mo Xiao-Dong, Huang Xiao-Jun, Sun Yu-Qian
Peking University People's Hospital and Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Beijing, China.
Blood Cell Ther. 2025 May 25;8(2):200-209. doi: 10.31547/bct-2024-034.
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.
本研究旨在评估程序性死亡受体1(PD-1)抗体对异基因造血干细胞移植(allo-HSCT)后伴有微小残留病(MRD)的急性髓系白血病(AML)或骨髓增生异常综合征(MDS)患者的疗效和安全性。本研究回顾性分析了6例患者,所有患者在使用PD-1抗体之前均接受过先前治疗(供体淋巴细胞输注或干扰素)但治疗失败。在这6例患者中,2例单独接受PD-1治疗,4例接受PD-1联合阿扎胞苷治疗。PD-1抗体的中位治疗剂量为4剂(范围为1-7剂)。3例患者出现3级以上毒性反应,其中2例死亡。在5例可评估的患者中,4例实现了MRD转阴,中位缓解时间为2个月(范围:1-3个月);中位缓解持续时间为105天(范围:26-211天)。这5例患者的中位生存时间为320天(范围:107-350天)。我们的数据表明,对于allo-HSCT后MRD呈阳性的AML/MDS患者,抗PD-1抗体可能是一种治疗选择。