Department of Obstetrics and Gynaecology, University Medical Centre Groningen, Groningen, The Netherlands.
Department of Radiotherapy, Erasmus University Medical Centre, Rotterdam, The Netherlands.
Nat Commun. 2024 Sep 3;15(1):7695. doi: 10.1038/s41467-024-52098-8.
Neoadjuvant immune checkpoint blockade (ICB) has shown unprecedented activity in mismatch repair deficient (MMRd) colorectal cancers, but its effectiveness in MMRd endometrial cancer (EC) remains unknown. In this investigator-driven, phase I, feasibility study (NCT04262089), 10 women with MMRd EC of any grade, planned for primary surgery, received two cycles of neoadjuvant pembrolizumab (200 mg IV) every three weeks. A pathologic response (primary objective) was observed in 5/10 patients, with 2 patients showing a major pathologic response. No patient achieved a complete pathologic response. A partial radiologic response (secondary objective) was observed in 3/10 patients, 5/10 patients had stable disease and 2/10 patients were non-evaluable on magnetic resonance imaging. All patients completed treatment without severe toxicity (exploratory objective). At median duration of follow-up of 22.5 months, two non-responders experienced disease recurrence. In-depth analysis of the loco-regional and systemic immune response (predefined exploratory objective) showed that monoclonal T cell expansion significantly correlated with treatment response. Tumour-draining lymph nodes displayed clonal overlap with intra-tumoural T cell expansion. All pre-specified endpoints, efficacy in terms of pathologic response as primary endpoint, radiologic response as secondary outcome and safety and tolerability as exploratory endpoint, were reached. Neoadjuvant ICB with pembrolizumab proved safe and induced pathologic, radiologic, and immunologic responses in MMRd EC, warranting further exploration of extended neoadjuvant treatment.
新辅助免疫检查点阻断(ICB)在错配修复缺陷(MMRd)结直肠癌中显示出前所未有的活性,但在 MMRd 子宫内膜癌(EC)中的有效性尚不清楚。在这项由研究者驱动的、I 期、可行性研究(NCT04262089)中,10 名任何分级的 MMRd EC 女性患者计划进行初始手术,接受两周期新辅助派姆单抗(200mg IV),每 3 周一次。在 5/10 名患者中观察到病理缓解(主要终点),其中 2 名患者表现出主要病理缓解。没有患者达到完全病理缓解。在 3/10 名患者中观察到部分放射学缓解(次要终点),5/10 名患者疾病稳定,2/10 名患者磁共振成像不可评估。所有患者均无严重毒性(探索性终点)完成治疗。在 22.5 个月的中位随访期间,2 名无反应者发生疾病复发。对局部和全身免疫反应的深入分析(预先设定的探索性终点)表明,单克隆 T 细胞扩增与治疗反应显著相关。肿瘤引流淋巴结与肿瘤内 T 细胞扩增存在克隆重叠。所有预定的终点,包括作为主要终点的病理缓解、作为次要终点的放射学缓解以及安全性和耐受性作为探索性终点,均达到。新辅助 ICB 联合派姆单抗在 MMRd EC 中证明是安全的,并诱导了病理、放射学和免疫反应,值得进一步探索扩展的新辅助治疗。