Clinical efficacy of nivolumab-based therapy for HER2-negative diffuse-type advanced gastric or gastroesophageal junction adenocarcinoma with peritoneal dissemination

Y. Suzuki , K. Shimozaki , S. Udagawa , K. Chin , H. Osumi , S. Fukuoka , K. Yoshino , M. Tamba , T. Wakatsuki , M. Ogura , E. Shinozaki , K. Yamaguchi , A. Ooki
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Abstract

Background

Diffuse-type gastric or gastroesophageal junctional cancers (DGC) often presents with peritoneal dissemination, leading to poor prognosis. This study assessed the efficacy of nivolumab-based therapies in patients with human epidermal growth factor receptor 2-negative DGC with peritoneal dissemination.

Materials and methods

This retrospective analysis included patients with DGC treated between June 2017 and March 2024. One cohort (n = 185) received nivolumab monotherapy as a third- or later-line treatment; the other (n = 117) received nivolumab plus chemotherapy as a first-line treatment.

Results

In the monotherapy cohort, 150 (81%) of 185 patients had peritoneal dissemination, which was significantly associated with worse progression-free survival (1.6 versus 2.5 months, P = 0.03) and overall survival (OS: 4.5 versus 7.2 months, P = 0.01) compared with those without peritoneal dissemination. In the first-line cohort, 74 (63%) of 117 patients had peritoneal dissemination. No significant differences were observed in progression-free survival (6.5 versus 9.6 months, P = 0.14) and OS (15.5 and 25.0 months, P = 0.47) between patients with and without peritoneal dissemination. Patients with peritoneal dissemination exhibited poor disease control in both cohorts, but those achieving complete or partial response had longer OS. The modified Glasgow Prognostic Score significantly impacted prognostic outcomes in both cohorts, while programmed death-ligand 1 status showed no statistical significance. Adverse events were manageable, with no treatment-related deaths.

Conclusions

First-line nivolumab plus chemotherapy demonstrated limited efficacy in human epidermal growth factor receptor 2-negative DGC with peritoneal dissemination but achieved a comparable OS to patients without peritoneal dissemination, supporting its potential as a first-line treatment.
尼武单抗治疗伴有腹膜播散的her2阴性弥漫性晚期胃或胃食管交界处腺癌的临床疗效
背景弥漫性胃癌或胃食管结癌(DGC)常表现为腹膜播散,预后较差。本研究评估了以尼伏单抗为基础的治疗方法对伴有腹膜播散的人表皮生长因子受体2阴性DGC患者的疗效。材料和方法本回顾性分析纳入2017年6月至2024年3月期间接受DGC治疗的患者。一个队列(n = 185)接受纳武单抗单药治疗作为三线或后期治疗;另一组(n = 117)接受纳武单抗加化疗作为一线治疗。结果在单药治疗队列中,185例患者中有150例(81%)存在腹膜播散,与未进行腹膜播散的患者相比,无进展生存期(1.6个月对2.5个月,P = 0.03)和总生存期(OS: 4.5个月对7.2个月,P = 0.01)较差。在一线队列中,117例患者中有74例(63%)发生腹膜播散。有无腹膜播散患者的无进展生存期(6.5个月vs 9.6个月,P = 0.14)和OS(15.5个月vs 25.0个月,P = 0.47)无显著差异。腹膜播散患者在两组中均表现出较差的疾病控制,但获得完全或部分缓解的患者有较长的生存期。改良后的格拉斯哥预后评分对两组患者的预后均有显著影响,而程序性死亡配体1状态无统计学意义。不良事件可控,无治疗相关死亡。结论:一线纳沃单抗加化疗对伴有腹膜播散的人表皮生长因子受体2阴性DGC的疗效有限,但与无腹膜播散的患者的OS相当,支持其作为一线治疗的潜力。
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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