免疫治疗加化疗作为局部晚期胃癌新辅助治疗的安全性和有效性:一项回顾性队列研究。

IF 3 3区 医学 Q2 ONCOLOGY Investigational New Drugs Pub Date : 2023-08-01 DOI:10.1007/s10637-023-01379-y
Xue Wang, Jinxiang Huang, He Huang, Yang Liu, Chao Ji, Jian Liu
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引用次数: 0

摘要

背景:程序性死亡受体-1 (PD-1)抑制剂和化疗的联合使用重塑了晚期或转移性胃癌(GC)的治疗前景。本研究旨在评估PD-1抑制剂联合化疗在局部晚期胃癌(LAGC)新辅助治疗中的有效性和安全性。方法:2019年12月至2022年7月,入选临床II-III期胃癌患者,接受新辅助PD-1抑制剂联合化疗。记录和分析临床病理特征、病理信息和生存资料。结果:共有42例符合条件的患者入组,其中37例(88.1%)为临床III期疾病。所有患者均行手术治疗,R0切除率为90.5%。主要病理缓解率(MPR)和病理完全缓解率(pCR)分别为42.9%和26.2%。总体TNM降期率为76.2%。36例(85.7%)患者接受了辅助化疗。中位随访23.1个月,肿瘤复发后死亡4例,复发后存活3例。1年总生存率(OS)和无病生存率(DFS)分别为94.4%和89.5%,中位OS和DFS未达到。新辅助治疗耐受性良好,未观察到4-5级治疗相关不良事件(TRAEs)。最常见的3级trae是贫血和丙氨酸转氨酶升高(n = 2, 9.6%)。结论:PD-1抑制剂联合化疗显示出有希望的疗效,在新辅助环境下对LAGC患者具有令人鼓舞的pCR和生存结果。联合治疗也显示出良好的安全性。
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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Safety and efficacy of immunotherapy plus chemotherapy as neoadjuvant treatment for patients with locally advanced gastric cancer: a retrospective cohort study.

Background: The combined use of programmed death receptor-1 (PD-1) inhibitors and chemotherapy has reshaped the treatment landscape of advanced or metastatic gastric cancer (GC). This study aimed to assess the efficacy and safety of PD-1 inhibitors combined with chemotherapy in a neoadjuvant setting for locally advanced GC (LAGC).

Methods: Patients diagnosed with clinical stage II-III GC undergoing neoadjuvant PD-1 inhibitors plus chemotherapy were enrolled from December 2019 to July 2022. Clinicopathological characteristics, pathological information, and survival data were recorded and analyzed.

Results: A total of 42 eligible patients were enrolled, of whom 37 (88.1%) had clinical stage III disease. All the patients underwent surgery, and the R0 resection rate was 90.5%. Major pathological response (MPR) and pathological complete response (pCR) rates were 42.9% and 26.2%, respectively. The overall TNM downstaging rate was 76.2%. A total of 36 (85.7%) patients received adjuvant chemotherapy. With a median follow-up of 23.1 months, four patients died after tumor recurrence, and three were alive with recurrence. The 1-year overall survival (OS) and disease-free survival (DFS) rates were 94.4% and 89.5%, respectively, and the median OS and DFS were not reached. Neoadjuvant treatment was well tolerated with no grade 4-5 treatment-related adverse events (TRAEs) observed. The most common grade 3 TRAEs were anemia and alanine aminotransferase increase (n = 2 each, 9.6%).

Conclusions: PD-1 inhibitors plus chemotherapy demonstrated promising efficacy, with encouraging pCR and survival outcomes in a neoadjuvant setting for patients with LAGC. The combined therapy also showed a good safety profile.

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来源期刊
CiteScore
7.60
自引率
0.00%
发文量
121
审稿时长
1 months
期刊介绍: The development of new anticancer agents is one of the most rapidly changing aspects of cancer research. Investigational New Drugs provides a forum for the rapid dissemination of information on new anticancer agents. The papers published are of interest to the medical chemist, toxicologist, pharmacist, pharmacologist, biostatistician and clinical oncologist. Investigational New Drugs provides the fastest possible publication of new discoveries and results for the whole community of scientists developing anticancer agents.
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