Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins University, Baltimore, Maryland, USA.
Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins, Baltimore, Maryland, USA.
Head Neck. 2022 Feb;44(2):562-571. doi: 10.1002/hed.26935. Epub 2021 Nov 26.
Given the recent successes of anti-PD-1 immunotherapy, many clinical trials have sought to assess the safety and efficacy of this treatment modality in the neoadjuvant setting. This systematic review provides a comprehensive summary of findings from neoadjuvant head and neck cancer immunotherapy clinical trials with a focus on PD-1/PD-L1 axis blockade. Pubmed, Embase, Cochrane Library, Web of Science, Google Scholar, and clinicaltrials.gov were systematically searched for all eligible neoadjuvant head and neck cancer immunotherapy clinical trials. Eight clinical trials met the inclusion criteria comprising a total of 260 patients. Study drugs included nivolumab, pembrolizumab, ipilimumab, durvalumab, and tremelimumab. The overall mean objective response rate (ORR) was 45.9 ± 5.7% with a 41.5 ± 5.6% single agent mean ORR. There were no deaths due to immune-related toxicities. Neoadjuvant immunotherapy for mucosal head and neck squamous cell cancer has demonstrated favorable response rates with no unexpected immune-related toxicities in phase I/II clinical trials.
鉴于抗 PD-1 免疫疗法的近期成功,许多临床试验都试图评估这种治疗方式在新辅助治疗环境中的安全性和疗效。本系统评价综合总结了新辅助头颈部癌症免疫治疗临床试验的结果,重点关注 PD-1/PD-L1 轴阻断。通过系统检索 Pubmed、Embase、Cochrane 图书馆、Web of Science、Google Scholar 和 clinicaltrials.gov,查找所有符合条件的新辅助头颈部癌症免疫治疗临床试验。八项临床试验符合纳入标准,共纳入 260 例患者。研究药物包括纳武利尤单抗、帕博利珠单抗、伊匹单抗、度伐利尤单抗和替西木单抗。总体客观缓解率(ORR)为 45.9±5.7%,单药 ORR 为 41.5±5.6%。无免疫相关毒性导致的死亡。在 I/II 期临床试验中,黏膜头颈部鳞状细胞癌的新辅助免疫治疗显示出良好的缓解率,且无意外的免疫相关毒性。