Chowdhury Deepro, Pond Gregory R, Goffin John R
Windsor Regional Hospital, Windsor, ON N8W 2X3, Canada.
Escarpment Cancer Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, ON L8V 1C3, Canada.
Curr Oncol. 2025 Jul 31;32(8):435. doi: 10.3390/curroncol32080435.
CAPOX and FOLFOX are widely used chemotherapy regimens for colorectal cancer (CRC). The superiority of one regimen over the other in a real-world setting (RWE) could have significant clinical implications given their common use, but such RWE is limited. This study analyzed provincial database records of 13,461 Canadian patients treated from 2005 to 2017. The primary outcomes were rates of Emergency Department visits and/or hospitalizations (ED/H) and overall survival (OS). CAPOX was used less frequently (8.4%) than FOLFOX (91.6%), often in older patients ( < 0.003 for Stage I-III; < 0.001 for Stage IV). CAPOX recipients had shorter treatment durations (median 15 vs. 20 weeks, = 0.002) and higher unadjusted ED/H rates (60.8% vs. 50.9%, < 0.001), though this difference was nonsignificant on multivariate analysis (MVA) (HR 1.05 (0.92, 1.20), = 0.466). Patients receiving CAPOX had worse OS than those on FOLFOX, (5-year OS 70.1% vs. 77.2% ( < 0.001) non-metastatic; 16.6% vs. 33.2% ( < 0.001) metastatic). MVA confirmed inferior OS with CAPOX (HR 1.42, < 0.001). Other predictors of shorter OS included older age, male sex, comorbidities, rural residence, and lower income. This administrative data is at risk of bias but highlights the need for careful patient selection and informed treatment decision making.
CAPOX和FOLFOX是广泛用于治疗结直肠癌(CRC)的化疗方案。鉴于它们的广泛应用,在真实世界环境(RWE)中一种方案相对于另一种方案的优越性可能具有重大的临床意义,但此类真实世界研究有限。本研究分析了2005年至2017年期间接受治疗的13461名加拿大患者的省级数据库记录。主要结局是急诊就诊率和/或住院率(ED/H)以及总生存期(OS)。CAPOX的使用频率(8.4%)低于FOLFOX(91.6%),且常用于老年患者(I-III期患者中P<0.003;IV期患者中P<0.001)。接受CAPOX治疗的患者治疗持续时间较短(中位时间分别为15周和20周,P=0.002),未调整的ED/H率较高(60.8%对50.9%,P<0.001),尽管在多变量分析(MVA)中这种差异无统计学意义(风险比1.05(0.92,1.20),P=0.466)。接受CAPOX治疗的患者的总生存期比接受FOLFOX治疗的患者差(非转移性患者5年总生存率分别为70.1%对77.2%(P<0.001);转移性患者分别为16.6%对33.2%(P<0.001))。MVA证实CAPOX组的总生存期较差(风险比1.42,P<0.001)。总生存期较短的其他预测因素包括老年、男性、合并症、农村居住和低收入。这些管理数据存在偏差风险,但突出了谨慎选择患者和做出明智治疗决策的必要性。