Efficacy and safety of camrelizumab in combination with S-1 plus oxaliplatin sequenced by camrelizumab-based maintenance therapy as a first-line treatment for advanced gastric or gastroesophageal junction adenocarcinoma: a retrospective cohort study.

IF 2 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Journal of gastrointestinal oncology Pub Date : 2025-04-30 Epub Date: 2025-04-27 DOI:10.21037/jgo-2025-189
Wan-Ren Peng, Fei Zhang, Wen-Wen Ma, Jie Da, Han-Qing Yu, Lu-Lu Fan, Zhen-Ya Jia, Jing Xu, Zi-Cong Gao, Chang-Chun Shao, Guo-Ping Sun
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引用次数: 0

Abstract

Background: S-1 plus oxaliplatin (SOX) is a first-line standard-of-care treatment for patients with advanced gastric or gastroesophageal junction (G/GEJ) adenocarcinoma. Programmed cell death protein 1 (PD-1) inhibitors plus chemotherapy, including SOX have also shown promising outcomes in such patients. This study was performed to evaluate the efficacy and safety of camrelizumab plus SOX sequenced by camrelizumab-based maintenance therapy as a first-line treatment for advanced G/GEJ adenocarcinoma.

Methods: In total, 31 patients with an age of 18 years or older and newly diagnosed with human epidermal growth factor receptor 2 (HER2)-negative advanced G/GEJ adenocarcinoma who underwent camrelizumab in combination with SOX followed by camrelizumab plus S-1 from February 2020 to December 2023 were enrolled in the study. All patients were regularly followed up every 1-2 months. The primary endpoint of the study was progression-free survival (PFS). And the safety profiles were also assessed.

Results: As of December 31, 2023, 25 male and 6 female patients were enrolled. The median follow-up time was 14.6 months. The median PFS time of the patients treated with the combination regimen was 7.3 months [95% confidence interval (CI): 3.0-11.6]. In addition, the median overall survival (OS) time was 13.3 months (95% CI: 10.3-16.4), and the median duration of response (DoR) was 5.0 months (95% CI: 2.0-8.1). Moreover, the objective response rate (ORR) and disease control rate (DCR) were 71.0% and 87.1%, respectively. Further, the most commonly observed grade ≥3 adverse events (AEs) were increased gamma-glutamyltransferase (GGT) (9.7%) and a decreased neutrophil count (6.5%). No treatment-related deaths occurred.

Conclusions: First-line treatment with camrelizumab in combination with SOX sequenced by camrelizumab-based maintenance therapy demonstrated favorable outcomes for and was well tolerated by patients with advanced G/GEJ adenocarcinoma. Thus, it might serve as a first-line standard-of-care treatment for such patients. However, prospective randomized studies should be carried out to confirm the findings.

camrelizumab联合S-1 +奥沙利铂作为晚期胃或胃食管连接处腺癌一线治疗的疗效和安全性:一项回顾性队列研究。
背景:S-1联合奥沙利铂(SOX)是晚期胃或胃食管交界处(G/GEJ)腺癌患者的一线标准治疗。程序性细胞死亡蛋白1 (PD-1)抑制剂加化疗,包括SOX,在这类患者中也显示出有希望的结果。本研究旨在评估camrelizumab加SOX序列的camrelizumab维持治疗作为晚期G/GEJ腺癌一线治疗的有效性和安全性。方法:在2020年2月至2023年12月期间,共有31例年龄在18岁及以上的新诊断为人表皮生长因子受体2 (HER2)阴性的晚期G/GEJ腺癌患者接受了camrelizumab联合SOX治疗,随后又接受了camrelizumab加S-1治疗。所有患者每1-2个月定期随访一次。该研究的主要终点是无进展生存期(PFS)。同时也对安全性进行了评估。结果:截至2023年12月31日,纳入25例男性和6例女性患者。中位随访时间为14.6个月。联合方案治疗患者的中位PFS时间为7.3个月[95%置信区间(CI): 3.0-11.6]。此外,中位总生存期(OS)时间为13.3个月(95% CI: 10.3-16.4),中位反应持续时间(DoR)为5.0个月(95% CI: 2.0-8.1)。客观缓解率(ORR)为71.0%,疾病控制率(DCR)为87.1%。此外,最常见的≥3级不良事件(ae)是γ -谷氨酰转移酶(GGT)增加(9.7%)和中性粒细胞计数减少(6.5%)。无治疗相关死亡发生。结论:camrelizumab联合SOX (camrelizumab为基础的维持治疗)一线治疗对晚期G/GEJ腺癌患者显示出良好的结果,并且耐受性良好。因此,它可以作为这类患者的一线标准治疗。然而,应该进行前瞻性随机研究来证实这些发现。
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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
171
期刊介绍: ournal of Gastrointestinal Oncology (Print ISSN 2078-6891; Online ISSN 2219-679X; J Gastrointest Oncol; JGO), the official journal of Society for Gastrointestinal Oncology (SGO), is an open-access, international peer-reviewed journal. It is published quarterly (Sep. 2010- Dec. 2013), bimonthly (Feb. 2014 -) and openly distributed worldwide. JGO publishes manuscripts that focus on updated and practical information about diagnosis, prevention and clinical investigations of gastrointestinal cancer treatment. Specific areas of interest include, but not limited to, multimodality therapy, markers, imaging and tumor biology.
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