Efficacy and prognostic factors of PD-1 inhibitors combined with apatinib in advanced diffuse gastric cancer.

IF 2 4区 医学 Q3 ONCOLOGY
Neoplasma Pub Date : 2025-04-01 Epub Date: 2025-03-28 DOI:10.4149/neo_2025_241021N429
Beibei Chen, Huichen Zhao, Huihui Hu, Jinxi Huang, Yingjun Liu, Huifang Lv, Weifeng Xu, Jianzheng Wang, Caiyun Nie, Jing Zhao, Yunduan He, Saiqi Wang, Yuhang Wang, Xiaobing Chen
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引用次数: 0

Abstract

Refractory diffuse gastric cancer (DGC) is rising in incidence and has a bad prognosis. Individuals who are administered second-line or subsequent therapies frequently exhibit diminished physical fitness, rendering them inappropriate for intensive treatment. Despite this, PD-1 inhibitors and anti-angiogenesis drug apatinib have demonstrated efficacy in advanced gastric cancer. This study aimed to evaluate the effectiveness, prognostic factors, and safety of PD-1 inhibitors in combination with apatinib in advanced DGC. The present study is a retrospective analysis of 34 patients with advanced DGC treated with apatinib combined with PD-1 inhibitors in the Affiliated Cancer Hospital of Zhengzhou University from 2019 to 2022. Apatinib 250 mg was administered to patients once a day. The median progression-free survival (mPFS) and the median overall survival (mOS) were estimated using Kaplan-Meier curves, whereas objective response rate (ORR), disease control rate (DCR), prognostic variables, and adverse events were among the other outcomes. Data from 34 patients were collected, and the ORR was 5.9% (2 out of 34), while the DCR was 55.9% (19 out of 34). The mPFS was 2.5 months (95% CI: 1.9-3.0), while the mOS was 6.8 months (95% CI: 3.7-9.9). Log-rank univariate analysis indicated that the mOS of patients with carcinoembryonic antigen (CEA) levels <4.7 ng/ml (11.3 months, 95% CI: 7.1-15.5) was significantly different from those with levels ≥4.7 ng/ml (2.7 months, 95% CI: 0.0-6.1) (p=0.008). A notable disparity in mOS and mPFS was observed between patients with CA125 <35 U/ml (7.7 months, 95% CI: 3.6-11.9) and those with CA125 ≥35 U/ml (2.5 months, 95% CI: 1.9-3.0) (p=0.003), as well as between patients with lactate dehydrogenase (LDH) <245 U/l (11.3 months, 95% CI: 7.2-15.5) and those with LDH ≥245 U/l (2.2 months, 95% CI: 1.5-2.9) (p=0.007), and between patients with PLTs <350×109/l (7.5 months, 95% CI: 6.4-8.7) compared to those with PLTs ≥350×109/l (1.7 months, 95% CI: 0.0-3.9) (p=0.001). Multivariate Cox regression analysis indicated that CA125, LDH, and PLT levels were independent prognostic variables. The occurrence of grade 3 or 4 treatment-related adverse events was 17.6% (6/34). The study suggests that the integration of PD-1 inhibitors and apatinib in second-line and subsequent therapies demonstrated promising efficacy and acceptable safety in advanced DGC patients. The concentrations of CA125, LDH, and PLTs may serve as prognostic indicators for DGC.

PD-1抑制剂联合阿帕替尼治疗晚期弥漫性胃癌的疗效及影响预后的因素。
难治性弥漫性胃癌(DGC)发病率呈上升趋势,预后较差。接受二线或后续治疗的个体经常表现出身体素质下降,因此不适合进行强化治疗。尽管如此,PD-1抑制剂和抗血管生成药物阿帕替尼已被证明对晚期胃癌有效。本研究旨在评估PD-1抑制剂联合阿帕替尼治疗晚期DGC的有效性、预后因素和安全性。本研究回顾性分析了2019 - 2022年郑州大学附属肿瘤医院34例接受阿帕替尼联合PD-1抑制剂治疗的晚期DGC患者。患者给予阿帕替尼250 mg,每天1次。使用Kaplan-Meier曲线估计中位无进展生存期(mPFS)和中位总生存期(mOS),而其他结果包括客观缓解率(ORR)、疾病控制率(DCR)、预后变量和不良事件。收集34例患者的数据,ORR为5.9% (2 / 34),DCR为55.9%(19 / 34)。mPFS为2.5个月(95% CI: 1.9-3.0),而mOS为6.8个月(95% CI: 3.7-9.9)。Log-rank单变量分析表明,癌胚抗原(CEA)水平与患者的mOS呈正相关
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来源期刊
Neoplasma
Neoplasma 医学-肿瘤学
CiteScore
5.40
自引率
0.00%
发文量
238
审稿时长
3 months
期刊介绍: The journal Neoplasma publishes articles on experimental and clinical oncology and cancer epidemiology.
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