Menopausal hormone therapy and risk of gastrointestinal cancer: Nested case-control study within a prospective cohort, and meta-analysis

被引:76
|
作者
Green, Jane [1 ]
Czanner, Gabriela [1 ,2 ]
Reeves, Gillian [1 ]
Watson, Joanna [1 ]
Wise, Lesley [3 ,4 ]
Roddam, Andrew [1 ,5 ]
Beral, Valerie [1 ]
机构
[1] Univ Oxford, Canc Epidemiol Unit, Oxford OX3 7LF, England
[2] Univ Warwick, Dept Stat, Coventry CV4 7A, W Midlands, England
[3] Med & Healthcare Prod Regulatory Agcy, London SW1W 9SZ, England
[4] Takeda Global Res & Dev Ctr Europe Ltd, London WC2B 4AE, England
[5] Amgen Ltd, Ctr Observat Res, Uxbridge UB8 1DH, Middx, England
基金
英国医学研究理事会;
关键词
hormone therapy; cancer; colorectal cancer; oesophageal cancer; gastric cancer; menopause; LARGE-BOWEL-CANCER; ESTROGEN PLUS PROGESTIN; COLORECTAL-CANCER; REPLACEMENT THERAPY; COLON-CANCER; POSTMENOPAUSAL WOMEN; REPRODUCTIVE FACTORS; CLINICAL-TRIAL; FOLLOW-UP; PREVENTION;
D O I
10.1002/ijc.26236
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Use of menopausal hormone therapy (HT) has been associated with reduced risk of colorectal cancer; evidence for its effect on other gastrointestinal cancers is limited. We conducted a nested casecontrol study within a UK cohort, and meta-analyses combining our results with those from published studies. Our study included women aged 50+ in the UK General Practice Research Database (GPRD): 1,054 with oesophageal, 750 with gastric and 4,708 with colorectal cancer, and 5 age- and practice-matched controls per case. Relative risks (RRs) and 95% confidence intervals (CIs) for cancer in relation to prospectively-recorded HT prescriptions were estimated by conditional logistic regression. Women prescribed HT had a reduced risk of oesophageal cancer (adjusted RR for 1+ vs. no HT prescriptions, 0.68, 95% CI 0.530.88; p = 0.004), gastric cancer (0.75, 0.541.05; p = 0.1) and colorectal cancer (0.81, 0.730.90; p < 0.001). There were no significant differences in cancer risk by HT type, estimated duration of HT use or between past and current users. In meta-analyses, risks for ever vs. never use of HT were significantly reduced for all three cancers (summary RR for oesophageal cancer, 0.68, 0.550.84, p < 0.001; for gastric cancer, 0.78, 0.650.94, p = 0.008; for colorectal cancer, 0.84, 0.810.88, p < 0.001). In high-income countries, estimated incidence over 5 years of these three cancers combined in women aged 5064 was 2.9/1,000 in HT users and 3.6/1,000 in never users. The absolute reduction in risk of these cancers in HT users is small compared to the HT-associated increased risk of breast cancer.
引用
收藏
页码:2387 / 2396
页数:10
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