Efficacy and safety of second-line therapy by S-1 combined with sintilimab and anlotinib in pancreatic cancer patients with liver metastasis: a single-arm, phase II clinical trial

被引:4
|
作者
Qiu, Xin [1 ,2 ,3 ]
Lu, Changchang [3 ]
Sha, Huizi [1 ,2 ]
Zhu, Yahui [1 ,2 ]
Kong, Weiwei [1 ,2 ]
Tong, Fan [3 ]
Wang, Qiaoli [3 ]
Meng, Fanyan [1 ,2 ]
Liu, Baorui [1 ,2 ]
Du, Juan [1 ,2 ,3 ]
机构
[1] Nanjing Univ, Comprehens Canc Ctr Drum Tower Hosp, Med Sch, Nanjing, Peoples R China
[2] Nanjing Univ, Clin Canc Inst, Nanjing, Peoples R China
[3] Nanjing Univ Chinese Med, Comprehens Canc Ctr Drum Tower Hosp, Clin Coll Tradit Chinese & Western Med, Nanjing, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
基金
中国国家自然科学基金;
关键词
advanced pancreatic cancer; liver metastasis; S-1; immunotherapy; antiangiogenic therapy; CHEMOTHERAPY; CAMRELIZUMAB; BEVACIZUMAB; GEMCITABINE;
D O I
10.3389/fimmu.2024.1210859
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Pancreatic adenocarcinoma carries a grim prognosis, and there are few recognized effective second-line treatment strategies. We attempted to evaluate the efficacy and safety of a combination of S-1, sintilimab, and anlotinib as a second-line treatment in pancreatic cancer patients with liver metastasis.Methods Pancreatic cancer patients with liver metastases were recruited. S-1 was administered orally at 25 mg/m2 bid, anlotinib was administered orally at 12 mg qd from day 1 to day 14, and sintilimab was administered intravenously at 200 mg on day 1. This method was repeated every 21 days, and the therapeutic effect was evaluated every 3 cycles. The primary outcome was the objective response rate (ORR).Results Overall, 23 patients were enrolled in this study of whom 19 patients had objective efficacy evaluation. The ORR was 10.5% (95% CI 0.4%-25.7%) in the evaluable population. The progression-free survival (PFS) was 3.53 (95% CI 2.50-7.50) months, and the overall survival (mOS) was 8.53 (95% CI 4.97-14.20) months. Grade 3 adverse events were 26.1%, and no grade 4 or above adverse events occurred. High-throughput sequencing was performed on the tumor tissues of 16 patients; patients with HRD-H (n = 10) had shorter PFS than those with HRD-L (n = 6) (2.43 vs. 5.45 months; P = 0.043), but there was no significant difference in OS between the two groups (4.43 vs. 9.35 months; P = 0.11).Conclusions This study suggests the advantage of S-1 combined with sintilimab and anlotinib in extending OS as a second-line therapy in pancreatic cancer patients with liver metastasis. Clinical Trial Registration: ChiCTR2000030659Conclusions This study suggests the advantage of S-1 combined with sintilimab and anlotinib in extending OS as a second-line therapy in pancreatic cancer patients with liver metastasis. Clinical Trial Registration: ChiCTR2000030659
引用
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页数:11
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