Safety and efficacy of apatinib in combination with chemotherapy with or without immunotherapy versus chemotherapy alone as first-line treatment for advanced gastric cancer

IF 3 3区 医学 Q2 ONCOLOGY Investigational New Drugs Pub Date : 2024-02-17 DOI:10.1007/s10637-024-01423-5
Lele Chang, Xuemei Zhang, Qian Ma, Lingyang Kong, Yang Yu, Ji Tao, Qingwei Li
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Abstract

The specific first-line regimen for advanced gastric cancer (GC) is still controversial. The benefit of apatinib for first-line treatment of advanced GC remains unknown and needs to be further explored. Eighty-two patients with advanced GC treated in our institution from October 2017 to March 2023 were retrospectively reviewed. All individuals had her-2 negative GC and had received at least two cycles of first-line treatment, including 44 patients in the combination treatment group (apatinib in combination with chemotherapy with or without immunotherapy) and 38 patients in the simple chemotherapy group. We evaluated the efficacy and safety of apatinib in combination with chemotherapy with or without immunotherapy in the first-line treatment of advanced GC by comparing the efficacy, progression-free survival (PFS), and adverse events in two groups of patients. The median PFS of the simple chemotherapy group was 9.25 months (95% confidence interval (CI), 6.1–11.2 months), and that of the combination treatment group was 10.9 months (95% CI, 7.9–15.8 months), which was 1.65 months longer than the simple chemotherapy group. Statistically significant differences are shown (P = 0.022). The objective response rate (ORR) of the combination treatment group was 65.9%, and 36.8% in the simple chemotherapy group. Statistically significant differences are shown (P = 0.014). No serious (Grade IV) adverse events occurred in either group. Our study indicates that apatinib in combination with chemotherapy with or without immunotherapy as first-line treatment for advanced GC exhibits good anti-tumor activity and is well tolerated by patients.

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阿帕替尼联合化疗(含或不含免疫疗法)与单独化疗作为晚期胃癌一线治疗的安全性和有效性比较
晚期胃癌(GC)的具体一线治疗方案仍存在争议。阿帕替尼在晚期胃癌一线治疗中的获益仍是未知数,需要进一步探索。我们对2017年10月至2023年3月在我院接受治疗的82例晚期GC患者进行了回顾性研究。所有患者均为her-2阴性GC,接受过至少两个周期的一线治疗,其中联合治疗组(阿帕替尼联合化疗,联合或不联合免疫治疗)44例,单纯化疗组38例。我们通过比较两组患者的疗效、无进展生存期(PFS)和不良反应,评估了阿帕替尼联合化疗(无论有无免疫疗法)一线治疗晚期GC的有效性和安全性。单纯化疗组的中位无进展生存期为9.25个月(95%置信区间为6.1-11.2个月),联合治疗组为10.9个月(95%置信区间为7.9-15.8个月),比单纯化疗组延长了1.65个月。差异具有统计学意义(P = 0.022)。联合治疗组的客观反应率(ORR)为 65.9%,单纯化疗组为 36.8%。差异有统计学意义(P = 0.014)。两组患者均未发生严重(IV级)不良反应。我们的研究表明,阿帕替尼与化疗联合或不联合免疫疗法作为晚期GC的一线治疗具有良好的抗肿瘤活性,且患者耐受性良好。
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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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