医学
养生
临床终点
彭布罗利珠单抗
免疫疗法
癌症
胰腺癌
外科
放射外科
临床研究阶段
放射治疗
内科学
胰腺切除术
肿瘤科
易普利姆玛
转移
放射科
胰腺
总体生存率
存活率
进行性疾病
切除术
原发性肿瘤
外科切除术
生存分析
随访中值
化疗
作者
Valerie Lee,Apoorvaa S. Sachidanand,Christina Rodriguez,Junke Wang,Beth Onners,Hanfei Qi,Rose Parkinson,Thomas McPhaul,Jennifer N. Durham,Dan Ding,Amy Hacker-Prietz, MS, PA-C,Amol Narang,Dung T. Le,Ana De Jesus,Michael Pishvaian,Eric S. Christenson,Elizabeth D. Thompson,Robert A. Anders,Arsen Osipov,M. S. Weiss
标识
DOI:10.1038/s41467-026-69294-3
摘要
In this Phase II study (NCT02648282) of locally advanced pancreatic cancer (LAPC), 58 patients were enrolled and intended for an immunotherapy including GM-CSF-secreting allogeneic pancreatic cancer vaccine (GVAX) and pembrolizumab and stereotactic body radiation therapy (SBRT) following standard chemotherapy. Fifty-four evaluable patients received two cycles of immunotherapy and SBRT and reassessed for resectability. After resection or biopsy, patients received continued immunotherapy for two years. At a median follow-up of 19.6 months, the median distant metastasis free survival (DMFS), the primary endpoint, for all evaluable patients was 9.8 months. Secondary endpoint analysis shows that, of these, 35 patients (64.8%) were deemed potentially resectable, and 24 underwent R0/R1 resections. Resected patients had a majority of R0 resections (91.7%). The overall resection rate was 44.4%. Patients who underwent resection had a median DMFS of 20.3 months. Median overall survival (OS), a secondary endpoint, for all evaluable patients from the start of the immunotherapy was 21.8 months, with resected patients reaching 29.7 months and unresected patients at 12.1 months. From diagnosis, median OS was 28.2 months, with resected patients achieving 36.7 months, while unresected patients had 19.7 months. In conclusion, the combination of GVAX, pembrolizumab, and SBRT showed promising efficacy in LAPC patients with favorable survival outcomes, especially those who underwent R0/R1 resections. However, patients with unresectable disease still maintained significantly worse DMFS and OS. The regimen demonstrated a manageable safety profile.
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