转移性胃癌患者接受曲妥珠单抗与全身化疗的生存结局比较。

Gi-Young Ha, Sung-Hyun Yang, Hye-Jin Kang, Hyo-Lak Lee, Jin Kim, Yun-Ju Kim, Hang-Jong Yu, Jong-Inn Lee, Sung-Ho Jin
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引用次数: 2

摘要

目的:目前,曲妥珠单抗联合化疗是人表皮生长因子受体2 (HER2)阳性晚期或转移性胃癌(mGC)或食管胃结癌的标准一线治疗方案。然而,目前尚不清楚曲妥珠单抗联合化疗治疗her2阳性mGC的预后是否优于化疗作为一线治疗的her2阴性mGC。方法:我们进行了一项回顾性研究,比较2011年至2018年韩国癌症中心医院一线治疗曲妥珠单抗加化疗或仅化疗的mGC预后。单因素和多因素生存分析采用Kaplan-Meier法和Cox比例风险模型。结果:曲妥珠单抗组的中位总生存期为26.1个月,化疗组的中位总生存期为14.8个月(P=0.047)。曲妥珠单抗组的中位无进展生存期长于化疗组(23.4个月vs 9.2个月,P=0.026)。通过单因素分析,性别、年龄、世界卫生组织(WHO)组织学、HER2状态、原发肿瘤部位、疾病范围、病变数量、转移数量、疾病可测量性、既往胃切除术和化疗组具有统计学意义。通过多因素分析,病变数量、转移数量、既往胃切除术和曲妥珠单抗组(风险比,0.594;95%置信区间为0.384-0.921;P=0.020)是影响总生存的独立预后因素。结论:曲妥珠单抗联合化疗治疗her2阳性mGC的预后优于单纯化疗治疗her2阴性mGC。需要精心设计的前瞻性队列研究来证实本研究的结果。所有新诊断为mGC的患者应常规进行HER2检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparison of survival outcomes according of patients with metastatic gastric cancer receiving trastuzumab with systemic chemotherapy.

Comparison of survival outcomes according of patients with metastatic gastric cancer receiving trastuzumab with systemic chemotherapy.

Comparison of survival outcomes according of patients with metastatic gastric cancer receiving trastuzumab with systemic chemotherapy.

Comparison of survival outcomes according of patients with metastatic gastric cancer receiving trastuzumab with systemic chemotherapy.

Purpose: Currently, trastuzumab plus chemotherapy is the standard first-line therapy for human epidermal growth factor receptor 2 (HER2)-positive advanced or metastatic gastric cancer (mGC) or esophagogastric junction cancer. However, it is not clear whether the prognosis of HER2-positive mGC treated with trastuzumab plus chemotherapy is better than that of HER2-negative mGC treated with chemotherapy as the first-line therapy.

Methods: We performed a retrospective study comparing the prognosis of mGC according to first-line treatment with trastuzumab plus chemotherapy or chemotherapy only, at the Korea Cancer Center Hospital from 2011 to 2018. The Kaplan-Meier method and Cox proportional hazards model were used for univariate and multivariate survival analyses.

Results: The median overall survival of trastuzumab group was 26.1 months and that of chemotherapy group was 14.8 months (P=0.047). Trastuzumab group had a longer median progression-free survival than chemotherapy group (23.4 vs. 9.2 months, P=0.026). By univariate analysis, sex, age, World Health Organization (WHO) histology, HER2 status, primary tumor site, extent of disease, number of lesions, number of metastatic, measurability of disease, prior gastrectomy, and chemotherapy group are statistically significant. Using multivariate analysis, number of lesions, number of metastatic, prior gastrectomy, and trastuzumab group (hazard ratio, 0.594; 95% confidence interval, 0.384-0.921; P=0.020) were found to be independent prognostic factors of overall survival.

Conclusion: The result suggests prognosis of HER2-positive mGC treated by trastuzumab plus chemotherapy could be better than that of HER2-negative mGC treated by chemotherapy only. Well-designed prospective cohort studies are needed to confirm the results of this study. HER2 testing should be performed routinely in all patients newly diagnosed with mGC.

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