Camrelizumab plus apatinib as second-line treatment for advanced oesophageal squamous cell carcinoma (CAP 02): a single-arm, open-label, phase 2 trial.

Xiangrui Meng, Tao Wu, Yonggui Hong, Qingxia Fan, Zhonghai Ren, Yanzhen Guo, Xiuli Yang, Pei Shi, Jiamei Yang, Xianzhe Yin, Zhiquan Luo, Jin Xia, Yue Zhou, Mengli Xu, Enjie Liu, Guozhong Jiang, Shenglei Li, Feng Zhao, Chi Ma, Chuanxiang Ma, Zhiguo Hou, Jing Li, Junsheng Wang, Feng Wang
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引用次数: 24

Abstract

Background: Camrelizumab, an anti-PD-1 antibody, has shown moderate efficacy in oesophageal squamous cell carcinoma. Apatinib, a selective inhibitor of VEGFR2, has a synergistic effect with immunotherapy. We aimed to assess the combination of camrelizumab and apatinib as second-line treatment for advanced oesophageal squamous cell carcinoma.

Methods: This single-arm, open-label, phase 2 study was conducted at eight centres in China. Eligible patients were aged 18-75 years, with an Eastern Cooperative Oncology Group performance status of 0 or 1, who had unresectable locally advanced, locally recurrent, or metastatic oesophageal squamous cell carcinoma, and had progressed after or were intolerant to first-line chemotherapy. Patients received intravenous camrelizumab 200 mg once every 2 weeks plus oral apatinib 250 mg once daily for a 28-day cycle until disease progression, unacceptable adverse events, or withdrawal of consent. The primary endpoint was investigator-assessed confirmed objective response rate. Efficacy was analysed in patients who had received at least one dose of study drug, and safety was analysed in patients who received the study drug and had at least one post-baseline safety assessment. The study of this cohort is complete and this trial is registered with ClinicalTrials.gov, number NCT03736863.

Findings: Between Dec 5, 2019, and Feb 10, 2021, 52 patients were enrolled and included in analyses. At data cutoff (June 20, 2021), median follow-up was 7·5 months (IQR 4·0-11·2). 18 (34·6%, [95% CI 22·0-49·1]) of 52 patients had a confirmed objective response. 23 (44%) of 52 patients had grade 3 or worse treatment-related adverse events. The most common grade 3 or worse treatment-related adverse events were increased aspartate aminotransferase (10 [19%]), increased gamma-glutamyltransferase (10 [19%]), and increased alanine aminotransferase (five [10%]). No treatment-related deaths occurred.

Interpretation: Camrelizumab combined with apatinib showed promising activity and manageable toxicity, and might be a potential second-line treatment option for patients with advanced oesophageal squamous cell carcinoma. Another cohort of this study, enrolling patients previously treated with first-line immunotherapy, is ongoing.

Funding: Jiangsu Hengrui Pharmaceuticals.

Camrelizumab联合阿帕替尼作为晚期食管鳞状细胞癌(CAP 02)的二线治疗:单组,开放标签,2期试验
背景:Camrelizumab是一种抗pd -1抗体,在食管鳞状细胞癌中显示出中等疗效。Apatinib是一种VEGFR2选择性抑制剂,与免疫治疗具有协同作用。我们的目的是评估camrelizumab和apatinib联合作为晚期食管鳞状细胞癌的二线治疗。方法:这项单臂、开放标签、2期研究在中国的8个中心进行。符合条件的患者年龄为18-75岁,东部肿瘤合作组表现状态为0或1,患有不可切除的局部晚期、局部复发或转移性食管鳞状细胞癌,在一线化疗后进展或不耐受。患者接受静脉注射camrelizumab 200 mg,每2周1次,加口服阿帕替尼250 mg,每天1次,28天周期,直到疾病进展,不可接受的不良事件,或撤回同意。主要终点是研究者评估确认的客观缓解率。对接受至少一剂研究药物的患者进行疗效分析,对接受研究药物并至少进行一次基线后安全性评估的患者进行安全性分析。该队列研究已经完成,该试验已在ClinicalTrials.gov注册,编号NCT03736863。研究结果:在2019年12月5日至2021年2月10日期间,52名患者入组并纳入分析。截至数据截止(2021年6月20日),中位随访时间为7.5个月(IQR为4.0 - 11.2)。52例患者中有18例(34.6%,[95% CI 22.0 ~ 49.1])客观缓解。52例患者中有23例(44%)发生3级或更严重的治疗相关不良事件。最常见的3级或更严重的治疗相关不良事件是天冬氨酸转氨酶升高(10例[19%])、γ -谷氨酰转氨酶升高(10例[19%])和丙氨酸转氨酶升高(5例[10%])。无治疗相关死亡发生。解释:Camrelizumab联合阿帕替尼显示出良好的活性和可控的毒性,可能是晚期食管鳞状细胞癌患者的潜在二线治疗选择。该研究的另一个队列正在进行中,纳入了以前接受过一线免疫治疗的患者。资助:江苏恒瑞药业。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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