新辅助辛替单抗和化疗后经口手术治疗hpv阳性可切除口咽癌:单臂,双中心,2期试验。

IF 10 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
EClinicalMedicine Pub Date : 2025-07-29 eCollection Date: 2025-08-01 DOI:10.1016/j.eclinm.2025.103393
Shida Yan, Xing Zhang, Fengjiao Li, Ankui Yang, Hui Li, Wanming Hu, Qiaohong Lin, Xiyuan Li, Mingyuan Du, Jingtao Chen, Guodong Man, Jianwei Zhang, Xuemei Fang, Li Ning, Shiting Zhang, Lili Han, Yanmei Ma, Jun Wang, Shuwei Chen, Ming Song
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引用次数: 0

摘要

背景:去强化治疗,如新辅助免疫化疗和经口手术,在人乳头瘤病毒相关的口咽鳞状细胞癌(HPV+OPSCC)中显示出希望,但仍在研究中。我们的目的是探讨新辅助免疫化疗的有效性和安全性,以及序贯经口手术治疗可切除HPV+OPSCC的可行性。方法:在这项单臂、双中心、2期试验中,招募可切除的HPV+OPSCC(临床分期T2-4N0-3M0)患者,每3周接受新辅助辛替单抗、顺铂和nab-紫杉醇两个周期的治疗,随后进行经口手术,包括经口机器人手术(TORS)。主要终点是主要病理反应(MPR),定义为原发病变中残余存活肿瘤小于或等于10%。该研究已在中国临床试验注册中心注册(ChiCTR2200058650),并正在进行中。研究结果:在2022年4月13日至2023年11月17日期间,27例患者入组,均接受了2个周期的新辅助免疫化疗,均获得部分缓解。其中根治性手术25例,其中经口手术21例,经口手术4例。24例(24/25,96.0%)患者达到MPR,其中17例(17/25,68.0%)患者达到病理完全缓解(pCR)。27例患者中有24例(88.9%)发生1-2级治疗相关不良事件(TRAE),包括皮疹(12/27,44.4%)、脱发(10/27,37.0%)、恶心(8/27,29.6%)、疲劳(8/27,29.6%)和疼痛(8/27,29.6%)。只有1例(1/ 27,3.7%)发生3级trae,无治疗相关死亡。对于按方案人群,2年DFS和OS均为96.0% (95% CI: 88.6%-100.0%)。大多数患者在术后3个月出现疼痛和吞咽等症状改善,并在术后6个月和1年保持稳定。循环肿瘤HPV-DNA清除在pCR患者中有发生的趋势。解释:对于可切除的HPV+OPSCC患者,新辅助免疫化疗和序贯经口手术(包括TORS)似乎是一种可行的策略,可产生有利的肿瘤和功能结果。资助:innovative Biologics。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Neoadjuvant sintilimab and chemotherapy followed by transoral surgery for HPV-positive resectable oropharyngeal cancer: a single-arm, two-centre, phase 2 trial.

Neoadjuvant sintilimab and chemotherapy followed by transoral surgery for HPV-positive resectable oropharyngeal cancer: a single-arm, two-centre, phase 2 trial.

Neoadjuvant sintilimab and chemotherapy followed by transoral surgery for HPV-positive resectable oropharyngeal cancer: a single-arm, two-centre, phase 2 trial.

Neoadjuvant sintilimab and chemotherapy followed by transoral surgery for HPV-positive resectable oropharyngeal cancer: a single-arm, two-centre, phase 2 trial.

Neoadjuvant sintilimab and chemotherapy followed by transoral surgery for HPV-positive resectable oropharyngeal cancer: a single-arm, two-centre, phase 2 trial.

Neoadjuvant sintilimab and chemotherapy followed by transoral surgery for HPV-positive resectable oropharyngeal cancer: a single-arm, two-centre, phase 2 trial.

Neoadjuvant sintilimab and chemotherapy followed by transoral surgery for HPV-positive resectable oropharyngeal cancer: a single-arm, two-centre, phase 2 trial.

Background: Treatment deintensification, such as neoadjuvant immunochemotherapy and transoral surgery, has shown promise but remains under investigation in human papillomavirus-associated oropharyngeal squamous cell carcinoma (HPV+OPSCC). We aimed to explore the efficacy and safety of neoadjuvant immunochemotherapy and the feasibility of sequential transoral surgery in patients with resectable HPV+OPSCC.

Methods: In this single-arm, two-centre, phase 2 trial, patients with resectable HPV+OPSCC (clinical stage T2-4N0-3M0) were recruited and received two cycles of neoadjuvant sintilimab, cisplatin, and nab-paclitaxel every three weeks, followed by transoral surgery, including transoral robotic surgery (TORS). The primary endpoint was major pathological response (MPR), defined as the residual viable tumor of less than or equal to 10% in the primary lesion. The study is registered with Chinese Clinical Trial Registry (ChiCTR2200058650) and is ongoing.

Findings: Between April 13, 2022 and November 17, 2023, 27 patients were enrolled and all received two cycles of neoadjuvant immunochemotherapy, which all achieved partial responses. Among them, 25 patients received radical surgery (21 TORSs and 4 transoral surgeries). MPR was achieved in 24 patients (24/25, 96.0%), including 17 (17/25, 68.0%) with pathological complete response (pCR). Grade 1-2 treatment-related adverse events (TRAE) occurred in 24 of 27 patients (88.9%), including skin rash (12/27, 44.4%), alopecia (10/27, 37.0%), nausea (8/27, 29.6%), fatigue (8/27, 29.6%), and pain (8/27, 29.6%). Only one patient (1/27, 3.7%) experienced grade 3 TRAEs with no treatment-related death. For the per-protocol population, the 2-year DFS and OS were both 96.0% (95% CI: 88.6%-100.0%). Most patients experienced improved symptoms including pain and swallowing at 3 months post-surgery, and remained stable at 6 months and 1 year post-surgery. Circulating tumor HPV-DNA clearance had a trend to occur in patients with pCR.

Interpretation: Neoadjuvant immunochemotherapy and sequential transoral surgery, including TORS, appears to be a feasible strategy that yields favorable oncologic and functional outcomes for patients with resectable HPV+OPSCC.

Funding: Innovent Biologics.

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来源期刊
EClinicalMedicine
EClinicalMedicine Medicine-Medicine (all)
CiteScore
18.90
自引率
1.30%
发文量
506
审稿时长
22 days
期刊介绍: eClinicalMedicine is a gold open-access clinical journal designed to support frontline health professionals in addressing the complex and rapid health transitions affecting societies globally. The journal aims to assist practitioners in overcoming healthcare challenges across diverse communities, spanning diagnosis, treatment, prevention, and health promotion. Integrating disciplines from various specialties and life stages, it seeks to enhance health systems as fundamental institutions within societies. With a forward-thinking approach, eClinicalMedicine aims to redefine the future of healthcare.
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