Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, California.
Department of Urology, University of California, San Francisco, California.
Cancer Epidemiol Biomarkers Prev. 2018 Apr;27(4):438-445. doi: 10.1158/1055-9965.EPI-17-0689. Epub 2018 Jan 22.
Marine ω-3 polyunsaturated fatty acids (PUFAs), primarily found in dark fish, may prevent colorectal cancer progression, in part through inhibition of prostaglandin-endoperoxide synthase 2 (PTGS2). However, data in humans are limited. We examined marine ω-3 PUFAs and fish intake and survival among 1,011 colon cancer patients enrolled in Cancer and Leukemia Group B 89803 between 1999 and 2001 and followed through 2009. Diet was assessed during and 6 months after chemotherapy. We used Cox proportional hazards regression to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for disease-free (DFS), recurrence-free (RFS), and overall survival (OS). We observed 343 recurrences and 305 deaths (median follow-up: 7 years). Patients in the highest vs. lowest quartile of marine ω-3 PUFA intake had an HR for DFS of 0.72 (95% CI, 0.54-0.97; = 0.03). Individuals who consumed dark fish ≥1/week versus never had longer DFS (HR 0.65; 95% CI, 0.48-0.87; -value = 0.007), RFS (HR 0.61; 95% CI, 0.46-0.86; = 0.007), and OS (HR 0.68; 95% CI, 0.48-0.96; = 0.04). In a subset of 510 patients, the association between marine ω-3 PUFA intake and DFS appeared stronger in patients with high PTGS2 expression (HR 0.32; 95% CI, 0.11-0.95; = 0.01) compared with patients with absent/low PTGS2 expression (HR 0.78; 95% CI, 0.48-1.27; = 0.35; = 0.19). Patients with high intake of marine ω-3 PUFAs and dark fish after colon cancer diagnosis may have longer DFS. Randomized controlled trials examining dark fish and/or marine ω-3 PUFA supplements and colon cancer recurrence/survival are needed. .
海洋 ω-3 多不饱和脂肪酸(PUFAs)主要存在于深色鱼类中,可能通过抑制前列腺素内过氧化物合酶 2(PTGS2)来预防结直肠癌的进展。然而,人体数据有限。我们研究了癌症和白血病组 B 89803 于 1999 年至 2001 年间招募的 1011 例结肠癌患者的海洋 ω-3 PUFAs 和鱼类摄入量与生存情况,并随访至 2009 年。在化疗期间和化疗后 6 个月评估饮食。我们使用 Cox 比例风险回归来估计无病生存期(DFS)、无复发生存期(RFS)和总生存期(OS)的风险比(HRs)和 95%置信区间(CIs)。我们观察到 343 例复发和 305 例死亡(中位随访时间:7 年)。最高与最低海洋 ω-3 PUFA 摄入量四分位数的患者的 DFS 风险比为 0.72(95%CI,0.54-0.97; = 0.03)。每周至少食用一次深色鱼类的个体比从不食用的个体具有更长的 DFS(HR 0.65;95%CI,0.48-0.87; 值 = 0.007)、RFS(HR 0.61;95%CI,0.46-0.86; = 0.007)和 OS(HR 0.68;95%CI,0.48-0.96; = 0.04)。在 510 例患者的亚组中,与无/低 PTGS2 表达的患者相比(HR 0.78;95%CI,0.48-1.27; = 0.35; = 0.19),海洋 ω-3 PUFA 摄入量与 DFS 之间的关联在 PTGS2 表达较高的患者中似乎更强(HR 0.32;95%CI,0.11-0.95; = 0.01)。在结直肠癌诊断后摄入大量海洋 ω-3 PUFAs 和深色鱼类的患者可能具有更长的 DFS。需要进行随机对照试验来检查深色鱼类和/或海洋 ω-3 PUFA 补充剂与结直肠癌复发/生存情况的关系。