鼻咽癌
阿帕蒂尼
粘膜炎
诱导化疗
放化疗
医学
肿瘤科
化疗
临床终点
内科学
存活率
临床试验
外科
胃肠病学
放射治疗
作者
Hu Liang,Yao-Fei Jiang,Guoying Liu,Lin Wang,Jianwei Wang,Nian Lu,Wei‐Xiong Xia,Liang‐Ru Ke,Yan‐Fang Ye,Jin-Lin Duan,Wei-Xin Bei,Shu-Hui Dong,Wang‐Zhong Li,Li‐Ting Liu,Chong Zhao,Changqing Xie,Yan‐Qun Xiang
标识
DOI:10.1038/s41467-024-45126-0
摘要
Abstract The antiangiogenic agent apatinib has been shown to clinically improve responses to immune checkpoint inhibitors in several cancer types. Patients with N3 nasopharyngeal carcinoma have a high risk of distant metastasis, however, if the addition of immunotherapy to standard treatment could improve efficacy is unclear. In this phase II clinical trial (ChiCTR2000032317), 49 patients with stage T any N3M0 nasopharyngeal carcinoma were enrolled and received the combination of three cycles of induction chemotherapy, camrelizumab and apatinib followed by chemoradiotherapy. Here we report on the primary outcome of distant metastasis-free survival and secondary end points of objective response rate, failure-free survival, locoregional recurrence-free survival, overall survival and toxicity profile. After induction therapy, all patients had objective response, including 13 patients (26.5%) with complete response. After a median follow-up of 28.7 months, the primary endpoint of 1-year distant metastasis-free survival was met for the cohort (1-year DMFS rate: 98%). Grade≥3 toxicity appeared in 32 (65.3%) patients, with the most common being mucositis (14[28.6%]) and nausea/vomiting (9[18.4%]). In this work, camrelizumab and apatinib in combination with induction chemotherapy show promising distant metastasis control with acceptable safety profile in patients with stage T any N3M0 nasopharyngeal carcinoma.
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