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PD-1抑制剂联合新辅助化疗治疗下咽癌和口咽癌的疗效

Efficacy of PD-1 inhibitor with neoadjuvant chemotherapy in hypopharyngeal and oropharyngeal cancer.

作者信息

Liu Xue-Ying, Shang-Guan Han-Jing, Zhang Wei, Chen Shuai, Luo Xian-Yang

机构信息

Department of Otolaryngology Head and Neck Surgery, The First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.

State Key Laboratory of Vaccines for Infectious Diseases, Xiang'an Biomedicine Laboratory, State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Innovation Platform for Industry-Education Integration in Vaccine Research, School of Public Health, Xiamen University, Xiamen, China.

出版信息

Front Oncol. 2024 Sep 24;14:1450830. doi: 10.3389/fonc.2024.1450830. eCollection 2024.

Abstract

OBJECTIVE

This study is aimed to evaluate the efficacy and safety of PD-1 inhibitors combined with neoadjuvant chemotherapy in patients with locally advanced hypopharyngeal and oropharyngeal cancer prior to surgical resection.

METHODS

This retrospective analysis included 42 patients diagnosed with locally advanced hypopharyngeal and oropharyngeal cancer. The efficacy, safety, survival, and laryngeal preservation rate were evaluated.

RESULTS

A total of 42 patients were included in this retrospective analysis, of whom 28 had hypopharyngeal cancer and 14 had oropharyngeal cancer. Of the 42 patients, 14 (33.3%) achieved a pathological complete response (PCR) at the primary site, 20 (47.6%) achieved a major pathological response (MPR), and 8 (19%) had an incomplete pathological response (IPR) at the primary lesion. A PCR at both the primary site and the neck lymph nodes was observed in 9 patients (21.4%). The laryngeal preservation rate was 92.9% (26/28) in patients with hypopharyngeal cancer. The median follow-up time was 10.5 months. The median progression-free survival (PFS) was 26.42 months (95% CI, 23.416-29.424), and the median overall survival (OS) was 27.1 months (95% CI, 24.316-29.884). The 1-year PFS rate was 83.1%, and the 1-year OS rate was 85.9%.

CONCLUSION

Combination therapy with PD-1 inhibitors and neoadjuvant chemotherapy has demonstrated superior efficacy and safety as a preoperative treatment for locally advanced hypopharyngeal and oropharyngeal cancer. Notably, this treatment regimen does not increase the risk of severe postoperative complications and has shown promising results in improving laryngeal preservation rates.

摘要

目的

本研究旨在评估程序性死亡受体1(PD-1)抑制剂联合新辅助化疗在局部晚期下咽癌和口咽癌患者手术切除前的疗效和安全性。

方法

这项回顾性分析纳入了42例诊断为局部晚期下咽癌和口咽癌的患者。评估了疗效、安全性、生存率和喉保留率。

结果

本回顾性分析共纳入42例患者,其中28例为下咽癌,14例为口咽癌。42例患者中,14例(33.3%)在原发部位达到病理完全缓解(PCR),20例(47.6%)达到主要病理缓解(MPR),8例(19%)在原发灶有不完全病理缓解(IPR)。9例患者(21.4%)在原发部位和颈部淋巴结均达到PCR。下咽癌患者的喉保留率为92.9%(26/28)。中位随访时间为10.5个月。中位无进展生存期(PFS)为26.42个月(95%CI,23.416-29.424),中位总生存期(OS)为27.1个月(95%CI,24.316-29.884)。1年PFS率为83.1%,1年OS率为85.9%。

结论

PD-1抑制剂联合新辅助化疗作为局部晚期下咽癌和口咽癌的术前治疗已显示出卓越的疗效和安全性。值得注意的是,该治疗方案不会增加严重术后并发症的风险,并且在提高喉保留率方面显示出了有前景的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c288/11458719/ee8fa2e56bbf/fonc-14-1450830-g001.jpg

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