首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Marine omega-3 fatty acid intake and survival of stage III colon cancer according to tumor molecular markers in NCCTG Phase III trial N0147 (Alliance)
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Marine omega-3 fatty acid intake and survival of stage III colon cancer according to tumor molecular markers in NCCTG Phase III trial N0147 (Alliance)

机译:海洋Omega-3脂肪酸摄入和阶段III结肠癌的存活,根据NCCTG期III试验N0147(联盟)的肿瘤分子标记

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摘要

Marine omega-3 polyunsaturated fatty acids (MO3PUFAs) have anticancer properties and may improve colon cancer survival. However, it remains unknown whether the benefit differs by tumor molecular subtype. We examined data from a phase III randomized trial of FOLFOX or FOLFOX + cetuximab among 1,735 stage III colon cancer patients who completed a dietary questionnaire at enrollment. Multivariable hazard ratios and 95% confidence intervals (CIs) were calculated for the association between MO3PUFA and disease-free survival (DFS) and overall survival according to KRAS and BRAF(V600E) mutations and DNA mismatch repair (MMR) status. Higher MO3PUFA intake was associated with improved 3-year DFS for KRAS wild-type tumors (77% vs. 73%; HR: 0.84; 95% CI: 0.67-1.05) but not KRAS-mutant tumors (64% vs. 70%; HR: 1.30; 95% CI: 0.97-1.73; P-interaction = 0.02). Similar heterogeneity was found by MMR (P-interaction = 0.14): higher MO3PUFA was associated with better 3-year DFS for tumors with deficient MMR (72% vs. 67%) but not proficient MMR (72% vs. 72%). No heterogeneity was found by BRAF(V600E) mutation. Similar findings were obtained for overall survival. In conclusion, we found a suggestive beneficial association between higher MO3PUFA intake and improved survival among stage III colon cancer patients with wild-type KRAS and deficient MMR. Given the relatively small number of cases with tumor molecular assessments, further studies, preferably through pooled analyses of multiples cohorts, are needed to validate our findings.
机译:海洋ω-3多不饱和脂肪酸(MO3PUFA)具有抗癌性质,可改善结肠癌存活。然而,它仍然未知是肿瘤分子亚型的益处是否与肿瘤分子亚型不同。我们在1,735阶段III结肠癌患者中检查了Folfox或Folfox + Cetuximab的III期随机试验中的数据。根据KRAS和BRAF(V600E)突变和DNA错配修复(MMR)状态,计算MO3PUFA与无病生存(DFS)和总存活的关联计算多变量危险比和95%置信区间(CIS)。较高的MO3PUFA摄入量与KRA野生型肿瘤的改善的3年DFS相关联(77%vs.73%; HR:0.84; 95%CI:0.67-1.05)但不是KRAS-突变肿瘤(64%与70% ; HR:1.30; 95%CI:0.97-1.73; p互动= 0.02)。通过MMR(p互动= 0.14)发现了类似的异质性:更高的MO3PUFA与缺乏MMR的肿瘤的更好的3年DFS相关(72%对67%)但不熟练的MMR(72%与72%)相关联。 BRAF(V600E)突变没有发现异质性。获得了同样的结果,用于整体存活。总之,我们发现较高MO3PUFA摄入量的暗示有益关联,并在III型结肠癌患者中提高了野生型KRAS和缺乏MMR的患者的存活。鉴于肿瘤分子评估的患者数量相对较少,需要进一步的研究,优选通过汇总群组的汇总分析来验证我们的研究结果。

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