Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Breast Cancer Res Treat. 2013 Jun;139(2):529-37. doi: 10.1007/s10549-013-2548-4. Epub 2013 May 10.
Vitamin supplement use after breast cancer diagnosis is common, but little is known about long-term effects on recurrence and survival. We examined postdiagnosis supplement use and risk of death or recurrence in the After Breast Cancer Pooling Project, a consortium of four cohorts of 12,019 breast cancer survivors from the United States and China. Post-treatment supplement use (vitamins A, B, C, D, E, and multivitamins) was assessed 1-5 years postdiagnosis. Associations with risk of recurrence, breast cancer-specific mortality, or total mortality were analyzed in Cox proportional hazards models separately by cohort. Individual cohort results were combined using random effects meta-analysis. Interactions with smoking, treatment, and hormonal status were examined. In multivariate models, vitamin E was associated with a decreased risk of recurrence (RR: 0.88; 95 % CI 0.79-0.99), and vitamin C with decreased risk of death (RR: 0.81; 95 % CI 0.72-0.92). However, when supplements were mutually adjusted, all associations were attenuated. There were no statistically significant associations with breast cancer mortality. The use of antioxidant supplements (multivitamins, vitamin C, or E) was not associated with recurrence, but was associated with a 16 % decreased risk of death (95 % CI 0.72-0.99). In addition, vitamin D was associated with decreased risk of recurrence among ER positive, but not ER negative tumors (p-interaction = 0.01). In this large consortium of breast cancer survivors, post-treatment use of vitamin supplements was not associated with increased risk of recurrence or death. Post-treatment use of antioxidant supplements was associated with improved survival, but the associations with individual supplement were difficult to determine. Stratification by ER status and considering antioxidants as a group may be more clinically relevant when evaluating associations with cancer risk and mortality.
乳腺癌诊断后补充维生素很常见,但对其长期对复发和生存的影响知之甚少。我们在美国和中国的四个队列的 12019 例乳腺癌幸存者组成的乳腺癌后汇集项目中,研究了诊断后补充剂的使用与死亡或复发的风险。治疗后(维生素 A、B、C、D、E 和多种维生素)的补充使用在诊断后 1-5 年内进行评估。使用 Cox 比例风险模型按队列分别分析与复发、乳腺癌特异性死亡率或总死亡率的相关性。使用随机效应荟萃分析组合个体队列结果。检查了与吸烟、治疗和激素状态的相互作用。在多变量模型中,维生素 E 与复发风险降低相关(RR:0.88;95%CI 0.79-0.99),维生素 C 与死亡风险降低相关(RR:0.81;95%CI 0.72-0.92)。然而,当补充剂相互调整时,所有相关性都减弱了。与乳腺癌死亡率无统计学显著相关性。抗氧化补充剂(多种维生素、维生素 C 或 E)的使用与复发无关,但与死亡风险降低 16%相关(95%CI 0.72-0.99)。此外,维生素 D 与 ER 阳性但 ER 阴性肿瘤的复发风险降低相关(p 交互作用=0.01)。在这个大型乳腺癌幸存者汇集项目中,治疗后使用维生素补充剂与复发或死亡风险增加无关。治疗后使用抗氧化补充剂与生存改善相关,但单个补充剂的相关性难以确定。根据 ER 状态分层并将抗氧化剂作为一组考虑时,在评估与癌症风险和死亡率的相关性时可能更具临床意义。