帕博利珠单抗联合二甲双胍治疗转移性头颈部癌的 II 期可行性研究
A Phase II Feasibility Study Combining Pembrolizumab and Metformin in Patients with Metastatic Head and Neck Cancer.
二甲双胍联合帕博利珠单抗耐受性良好,仅出现轻度胃肠道不良事件,并展现出有前景的活性,值得在随机试验中进一步研究。
英文原题:A Phase II Open-Label Randomized Clinical Trial of Preoperative Durvalumab or Durvalumab plus Tremelimumab in Resectable Head and Neck Squamous Cell Carcinoma.
术前D±T是可行的,可能使可切除HNSCC患者获益。每种治疗方案均诱导了肿瘤微环境和循环免疫细胞的显著变化,值得进一步研究。
新辅助免疫治疗在局部晚期但可切除的头颈部鳞状细胞癌(HNSCC)患者中的临床意义在很大程度上仍未被探索。
可切除HNSCC患者被随机分配接受术前单剂durvalumab(D)联合或不联合tremelimumab(T)治疗后进行切除,随后根据多学科判断接受术后(放)化疗及1年D治疗。人工智能(AI)驱动的TIL(肿瘤浸润淋巴细胞)空间分布分析及循环免疫细胞的高维分析追踪了动态的瘤内和全身免疫反应。
在入组的48例患者中(D组24例;D+T组24例),45例按方案接受了手术切除(D组21例;D+T组24例)。D±T具有良好的安全性特征,且未延迟手术。D+T治疗患者的远处无复发生存期(DRFS)显著优于D单药治疗患者。AI驱动的全切片图像分析表明,与D单药治疗或细胞毒性化疗相比,D+T显著重塑了肿瘤微环境,使其向免疫炎症表型转变。循环免疫细胞的高维分析显示,响应D+T治疗时,以增殖和活化为特征的T细胞亚群显著扩增,而这在D单药治疗后罕见。重要的是,CD8+ T细胞和非调节性CD4+ T细胞中具有活化和耗竭程序的特定簇的扩增,与接受D+T治疗患者的DRFS延长相关。
PURPOSE: Clinical implications of neoadjuvant immunotherapy in patients with locally advanced but resectable head and neck squamous cell carcinoma (HNSCC) remain largely unexplored. PATIENTS AND METHODS: Patients with resectable HNSCC were randomized to receive a single dose of preoperative durvalumab (D) with or without tremelimumab (T) before resection, followed by postoperative (chemo)radiotherapy based on multidisciplinary discretion and 1-year D treatment. Artificial intelligence (AI)-powered spatial distribution analysis of tumor-infiltrating lymphocytes and high-dimensional profiling of circulating immune cells tracked dynamic intratumoral and systemic immune responses. RESULTS: Of the 48 patients enrolled (D, 24 patients; D+T, 24 patients), 45 underwent surgical resection per protocol (D, 21 patients; D+T, 24 patients). D±T had a favorable safety profile and did not delay surgery. Distant recurrence-free survival (DRFS) was significantly better in patients treated with D+T than in those treated with D monotherapy. AI-powered whole-slide image analysis demonstrated that D+T significantly reshaped the tumor microenvironment toward immune-inflamed phenotypes, in contrast with the D monotherapy or cytotoxic chemotherapy. High-dimensional profiling of circulating immune cells revealed a significant expansion of T-cell subsets characterized by proliferation and activation in response to D+T therapy, which was rare following D monotherapy. Importantly, expansion of specific clusters in CD8+ T cells and non-regulatory CD4+ T cells with activation and exhaustion programs was associated with prolonged DRFS in patients treated with D+T. CONCLUSIONS: Preoperative D±T is feasible and may benefit patients with resectable HNSCC. Distinct changes in the tumor microenvironment and circulating immune cells were induced by each treatment regimen, warranting further investigation.
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