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Toripalimab combined with lenvatinib and GEMOX is a promising regimen as first-line treatment for advanced intrahepatic cholangiocarcinoma: a single-center, single-arm, phase 2 study

医学 吉西他滨 伦瓦提尼 奥沙利铂 内科学 养生 临床终点 不利影响 中性粒细胞减少症 肿瘤科 胃肠病学 索拉非尼 癌症 肝细胞癌 化疗 临床试验 结直肠癌
作者
Guo‐Ming Shi,Xiaoyong Huang,Dong Wu,Hui‐Chuan Sun,Fei Liang,Yuan Ji,Yi Chen,Guo‐Huan Yang,Jia‐Cheng Lu,Xian-Long Meng,Sheng Wang,Lei Sun,Ningling Ge,Xiaowu Huang,Shuang-Jian Qiu,Xin‐Rong Yang,Qiang Gao,Yifeng He,Yang Xu,Jian Sun,Zhenggang Ren,Jia Fan,Jian Zhou
出处
期刊:Signal Transduction and Targeted Therapy [Springer Nature]
卷期号:8 (1) 被引量:42
标识
DOI:10.1038/s41392-023-01317-7
摘要

Abstract Advanced intrahepatic cholangiocarcinoma (ICC) has a dismal prognosis. Here, we report the efficacy and safety of combining toripalimab, lenvatinib, and gemcitabine plus oxaliplatin (GEMOX) as first-line therapy for advanced ICC. Thirty patients with pathologically confirmed advanced ICC received intravenous gemcitabine (1 g/m 2 ) on Days 1 and 8 and oxaliplatin (85 mg/m 2 ) Q3W for six cycles along with intravenous toripalimab (240 mg) Q3W and oral lenvatinib (8 mg) once daily for one year. The expression of programmed death-ligand 1 (PD-L1) and genetic status was investigated in paraffin-embedded tissues using immunohistochemistry and whole-exome sequencing (WES) analysis. The primary endpoint was the objective response rate (ORR). Secondary outcomes included safety, overall survival (OS), progression-free survival (PFS), disease control rate (DCR) and duration of response (DoR). As of July 1, 2022, the median follow-up time was 23.5 months, and the ORR was 80%. Twenty-three patients achieved partial response, and one achieved complete response. Patients (21/30) with DNA damage response (DDR)-related gene mutations showed a higher ORR, while patients (14/30) with tumor area positivity ≥1 (PD-L1 staining) showed a trend of high ORR, but without significant difference. The median OS, PFS, and DoR were 22.5, 10.2, and 11.0 months, respectively. The DCR was 93.3%. Further, 56.7% of patients experienced manageable grade ≥3 adverse events (AEs), commonly neutropenia (40.0%) and leukocytopenia (23.3%). In conclusion, toripalimab plus lenvatinib and GEMOX are promising first-line regimens for the treatment of advanced ICC. A phase-III, multicenter, double-blinded, randomized study to validate our findings was approved by the National Medical Products Administration (NMPA, No. 2021LP01825). Trial registration Clinical trials : NCT03951597.
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