Updates from a single-center phase 2 study of PD-1 inhibitor combined with hypomethylating agent plus CAG regimen in patients with relapsed/refractory acute myeloid leukemia

作者：Hui-Sheng Zhou, Yong-Feng Su, Jun Wang, Ya-Lei Hu, An Wang, Lei Xu, Yizhi Wang, Xuan Zheng, Yuqing Li, Kai-Li Min, Chunji Gao, Dai‐Hong Liu, Xiaoning Gao · 发表于：Frontiers in Immunology · 年份：2025 · DOI：10.3389/fimmu.2025.1533467 · 被引用次数：3 · 研究领域：Acute Myeloid Leukemia Research、Immune cells in cancer、CAR-T cell therapy research

Introduction: Anti-PD-1 monotherapy has shown limited clinical efficacy in patients with relapsed/refractory acute myeloid leukemia (r/r AML). Our study aimed to analyze the effectiveness and safety of combining tislelizumab with a hypomethylating agent (HMA) plus CAG regimen in treating patients with r/r AML, with an increased sample size and in comparison, with a historical control group for more reliable data support (ClinicalTrials.gov identifier NCT04541277). Methods: The study included a total of 37 patients with r/r AML who received the tislelizumab + HMA + CAG regimen. Results: The overall response rate was 69.4%, with a median overall survival of 12.1 months and event-free survival of 6.2 months. Multivariate analysis revealed that patients aged 40 or above exhibited a higher response rate, while those with lower leukemia burden (bone marrow blast percentage <40%) demonstrated improved overall survival and event-free survival. Additionally, bridging allogeneic hematopoietic stem cell transplantation was associated with extended event-free survival. Grade 2-3 immune-related adverse events were observed in 8.5% of patients, and no deaths were directly attributed to these events. After propensity score matching, the inclusion of tislelizumab appeared to positively influence the overall response rate and event-free survival compared to historical controls treated with HMA + CAG regimen. Discussion: Overall, the combination regimen improved response rates while maintainin...