Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Non-Communicable Diseases Research Center, Endocrinology and Metabolism Population Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Daru. 2022 Dec;30(2):427-441. doi: 10.1007/s40199-022-00451-x. Epub 2022 Sep 22.
Association between vitamins C (VC)/ E (VE) and cancer survival is inconsistent. This systematic review is aimed to summarize trials for effects of VC/VE on cancer survival.
Relevant English trials were retrieved from PubMed, Cochrane Library, Embase, Web of Science, Scopus databases, and Clinicaltrials.gov through 21/June/2022. Inclusion criteria were all trials which assessed sole/combinations intake of VC/VE on survival rate, mortality, or remission of any cancer. Exclusion criteria were observational and animal studies.
We reached 30 trials conducted on 38,936 patients with various cancers. Due to severe methodological heterogeneity, meta-analysis was impossible. High dose VC + chemotherapy or radiation was safe with an overall survival (OS) 182 days - 21.5 months. Sole oral or intravenous high dose VC was safe with non-significant change in OS (2.9-8.2 months). VE plus chemotherapy was safe, resulted in stabling diseases for 5 years in 70- 86.7% of patients and OS 109 months. It was found 60% and 16% non-significant reductions in adjusted hazard ratio (HR) deaths or recurrence by 200 mg/d tocotrienol + tamoxifen in breast cancer, respectively. Sole intake of 200-3200 mg/d tocotrienol before resectable pancreatic cancer was safe and significantly increased cancer cells' apoptosis. Combination VC and VE was non-significantly reduced 7% in rate of neoplastic gastric polyp.
Although our study is supported improvement of survival and progression rates of cancers by VC/VE, more high quality trials with large sample sizes are required to confirm.
CRD42020152795.
维生素 C(VC)/E(VE)与癌症生存之间的关联不一致。本系统评价旨在总结 VC/VE 对癌症生存影响的试验。
通过 2022 年 6 月 21 日从 PubMed、Cochrane Library、Embase、Web of Science、Scopus 数据库和 Clinicaltrials.gov 检索到相关的英文试验。纳入标准为评估 VC/VE 单独或联合摄入对任何癌症的生存率、死亡率或缓解率的所有试验。排除标准为观察性和动物研究。
我们达成了 30 项针对 38936 名患有各种癌症的患者的试验。由于方法学上的严重异质性,无法进行 meta 分析。高剂量 VC+化疗或放疗是安全的,总生存率(OS)为 182 天-21.5 个月。单独口服或静脉内高剂量 VC 是安全的,OS 无显著变化(2.9-8.2 个月)。VE 加化疗是安全的,可使 70-86.7%的患者疾病稳定 5 年,OS 为 109 个月。在乳腺癌中,分别用 200mg/d 三烯生育酚+他莫昔芬和 16%非显著降低调整后的死亡或复发风险比(HR)。在可切除的胰腺癌前单独摄入 200-3200mg/d 的三烯生育酚是安全的,并显著增加了癌细胞的凋亡。VC 和 VE 的联合摄入可使胃息肉的发生率降低 7%,但无统计学意义。
尽管我们的研究表明 VC/VE 可改善癌症的生存率和进展率,但需要更多高质量、大样本量的试验来证实。
PROSPERO 注册号:CRD42020152795。