瑞戈非尼治疗转移性结直肠癌的治疗效果与化疗的副作用和加用情况:一项全人群队列研究

T.-C. Wu , Y.-H. Liang , K.-H. Chen , Y.-Y. Shao
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引用次数: 0

摘要

背景瑞戈非尼是转移性结直肠癌(mCRC)的挽救方案。了解接受瑞戈非尼治疗的mCRC患者的预后因素有助于优化治疗策略。材料与方法我们检索了台湾国民健康保险数据库中2015年9月1日至2018年12月31日期间开始接受瑞戈非尼治疗的mCRC患者。台湾国家死亡登记中心和台湾癌症登记中心分别对生存和临床病理变量数据进行了检查。结果共有 3643 例患者纳入分析。中位停止治疗时间(TTD)为2.3个月,中位总生存期(OS)为7.2个月。与右侧肿瘤患者相比,左侧原发肿瘤患者的治疗终止时间(2.4 个月对 2.1 个月,P < 0.001)和总生存期(7.6 个月对 6.1 个月,P < 0.001)明显更长。与未接受化疗的患者相比,接受瑞戈非尼化疗的患者的TTD(2.6个月对2.2个月,P< 0.001)和OS(8.3个月对6.7个月,P< 0.001)也更长。在多变量分析中,左侧和化疗加成被证实是延长TTD和OS的预测因素。由于左侧和 KRAS 突变之间存在交互作用,我们建立了单独的 Cox 模型,发现左侧是 KRAS 野生型肿瘤较长 TTD 和 OS 的独立预测因素,但不是 KRAS 突变肿瘤的预测因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sidedness and addition of chemotherapy associated with treatment outcomes of regorafenib for metastatic colorectal cancer: a population-wide cohort study

Background

Regorafenib is a salvage option for metastatic colorectal cancer (mCRC). Understanding the prognostic factors for mCRC patients undergoing regorafenib treatment can help optimize therapeutic strategies.

Materials and methods

We searched Taiwan’s National Health Insurance database for patients who began regorafenib treatment for mCRC between 1 September 2015 and 31 December 2018. Taiwan’s National Death Registry and the Taiwan Cancer Registry were examined for data on survival and clinicopathological variables, respectively.

Results

In total, 3643 patients were included in the analysis. The median time to treatment discontinuation (TTD) was 2.3 months, and the median overall survival (OS) was 7.2 months. Compared with the patients with a right-sided tumor, those with a left-sided primary tumor exhibited a significantly longer TTD (2.4 versus 2.1 months, P < 0.001) and OS (7.6 versus 6.1 months, P < 0.001). The patients who received chemotherapy with regorafenib also exhibited a longer TTD (2.6 versus 2.2 months, P < 0.001) and OS (8.3 versus 6.7 months, P < 0.001) than did the patients who did not. In multivariate analysis, left-sidedness and chemotherapy addition were confirmed as predictors of longer TTD and OS. Because of the interaction between sidedness and KRAS mutation, we established separate Cox models and identified that left-sidedness was an independent predictor of longer TTD and OS for KRAS wild-type tumors but not for KRAS-mutant tumors.

Conclusions

In this population-wide cohort study, left-sidedness of the primary tumor and the addition of chemotherapy were associated with a longer OS and TTD for regorafenib treatment for mCRC.

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