转移性胰腺癌的第一线修改型FOLFIRINOX:来自越南队列的现实世界结果和预后因素
Huy Van Nguyen1, Phuong Thi Dinh2, Thang Tran1
1Department of Medical Oncology, National Cancer Hospital, Hanoi, Vietnam.
Clinical Medicine Insights. Oncology
|March 2, 2026
概括
修改后的FOLFIRINOX (mFOLFIRINOX) 在越南的转移性胰腺癌中显示出有效性和可控毒性. 性能状态是这些患者整体生存的关键因素.
科学领域:
- 在瘤学瘤学.
- 胃肠病学 胃肠病学
- 临床研究 临床研究
背景情况:
- 转移性胰腺癌的预后不佳,尽管进行了化疗.
- 在低资源环境中对改性FOLFIRINOX (mFOLFIRINOX) 的现实数据有限.
- 这项研究的重点是接受mFOLFIRINOX作为一线治疗的越南患者.
研究的目的:
- 评估mFOLFIRINOX在越南转移性胰腺癌患者中的疗效和毒性.
- 确定影响该人口结果的预后因素.
- 评估mFOLFIRINOX在现实世界低资源医疗保健系统中的可行性.
主要方法:
- 对36名接受mFOLFIRINOX的患者进行了回顾性队列研究.
- 佩格-菲尔格拉斯蒂姆用于预防;允许灵活的治疗中断.
- 评估无进展生存期 (PFS),总生存期 (OS),瘤反应和不良事件.
- 使用日志等级测试和考克斯回归的预测因素分析.
主要成果:
- 随访时间中位数为15.6个月.
- 总体应答率 (ORR) 为30.6%,疾病控制率 (DCR) 为66.6%.
- 中位数PFS为6.7个月;中位数OS为12.5个月.
- 观察到3/4级的血液毒性 (中性质减退,贫血);没有发烧性中性质减退.
- 性能状态 (PS) 和年龄<60与更好的结果有关;PS是OS的独立预后因素.
结论:
- 在越南患有转移性胰腺癌的患者中,mFOLFIRINOX疗法是有效和可控的.
- 一种个性化治疗方法,中断与良好的结果相关.
- 研究结果支持mFOLFIRINOX在现实世界,资源有限的环境中的可行性.
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