Irreversible electroporation combined with chemotherapy and PD-1/PD-L1 blockade enhanced antitumor immunity for locally advanced pancreatic cancer

被引:8
作者
Ma, Yangyang [1 ]
Xing, Yanli [2 ]
Li, Hongmei [2 ]
Yuan, Ting [2 ]
Liang, Bing [3 ]
Li, Rongrong [4 ]
Li, Jianyu [3 ]
Li, Zhonghai [5 ]
Li, Shuying [3 ]
Niu, Lizhi [2 ]
机构
[1] Jinan Univ, Affiliated Fuda Canc Hosp, Cent Lab, Guangzhou 510665, Guangdong, Peoples R China
[2] Jinan Univ, Fuda Canc Hosp, Dept Oncol, Guangzhou 510665, Peoples R China
[3] Jinan Univ, Affiliated Fuda Canc Hosp, Dept Surg & Anesthesia, Guangzhou, Peoples R China
[4] Jinan Univ, Affiliated Fuda Canc Hosp, Dept Ultrasound, Guangzhou, Peoples R China
[5] Jinan Univ, Affiliated Fuda Canc Hosp, Dept Radiol, Guangzhou, Peoples R China
关键词
irreversible electroporation; locally advanced pancreatic cancer; chemotherapy; PD-1/PD-L1; blockade; anticancer immunity; PD-1; BLOCKADE; ADENOCARCINOMA; ABLATION;
D O I
10.3389/fimmu.2023.1193040
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BackgroundIrreversible electroporation (IRE) is a novel local tumor ablation approach with the potential to stimulate an antitumor immune response. However, it is not effective in preventing distant metastasis in isolation. This study aimed to compare the potential of augmenting the antitumor immune response in patients with locally advanced pancreatic cancer (LAPC) who underwent IRE combined with chemotherapy and PD-1/PD-L1 blockade with those who underwent IRE combined with chemotherapy.MethodsA retrospective review was conducted on LAPC patients treated either with IRE in combination with chemotherapy and PD-1/PD-L1 blockade (group A) or with IRE with chemotherapy alone (group B) from July 2015 to June 2021. The primary outcomes were overall survival (OS) and progression-free survival (PFS), with immune responses and adverse events serving as secondary endpoints. Risk factors for OS and PFS were identified using univariate and multivariate analyses.ResultsA total of 103 patients were included in the final analysis, comprising 25 in group A and 78 in group B. The median duration of follow-up was 18.2 months (3.0-38.6 months). Group A patients demonstrated improved survival compared to group B (median OS: 23.6 vs. 19.4 months, p = 0.001; median PFS: 18.2 vs. 14.7 months, p = 0.022). The data suggest a robust immune response in group A, while adverse events related to the treatment were similar in both groups. The multivariate analysis identified the combination of IRE, chemotherapy, and PD-1/PD-L1 blockade as an independent prognostic factor for OS and PFS.ConclusionThe addition of PD-1/PD-L1 blockade to the regimen of IRE combined with chemotherapy enhanced antitumor immunity and extended survival in LAPC patients.
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页数:13
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