Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study

被引:44
|
作者
Kehm, Rebecca D. [1 ]
Hopper, John L. [2 ]
John, Esther M. [3 ,4 ]
Phillips, Kelly-Anne [2 ,5 ,6 ]
MacInnis, Robert J. [2 ,7 ]
Dite, Gillian S. [2 ]
Milne, Roger L. [2 ,7 ,8 ]
Liao, Yuyan [1 ]
Zeinomar, Nur [1 ]
Knight, Julia A. [9 ,10 ]
Southey, Melissa C. [11 ]
Vahdat, Linda [12 ,13 ]
Kornhauser, Naomi [12 ]
Cigler, Tessa [14 ]
Chung, Wendy K. [15 ,16 ,17 ]
Giles, Graham G. [2 ,7 ]
McLachlan, Sue-Anne [18 ,19 ]
Friedlander, Michael L. [20 ,21 ]
Weideman, Prue C. [2 ]
Glendon, Gord [9 ]
Nesci, Stephanie [22 ]
Andrulis, Irene L. [9 ,24 ,25 ]
Buys, Saundra S. [26 ,27 ]
Daly, Mary B. [28 ]
Terry, Mary Beth [1 ,17 ]
机构
[1] Columbia Univ, Dept Epidemiol, Mailman Sch Publ Hlth, 722 W 168th St, New York, NY 10032 USA
[2] Univ Melbourne, Ctr Epidemiol & Biostat, Parkville, Vic 3010, Australia
[3] Stanford Univ, Dept Med, Sch Med, 780 Welch Rd, Stanford, CA 94304 USA
[4] Stanford Univ, Stanford Canc Inst, Sch Med, 780 Welch Rd, Stanford, CA 94304 USA
[5] Peter MacCallum Canc Ctr, Dept Med Oncol, 305 Grattan St, Melbourne, Vic 3000, Australia
[6] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic 3010, Australia
[7] Canc Council Victoria, Canc Epidemiol, 615 St Kilda Rd, Melbourne, Vic 3004, Australia
[8] Monash Univ, Precis Med, Sch Clin Sci, Monash Hlth, Clayton, Vic 3168, Australia
[9] Sinai Hlth Syst, Lunenfeld Tanenbaum Res Inst, 600 Univ Ave, Toronto, ON M5G 1X5, Canada
[10] Univ Toronto, Dalla Lana Sch Publ Hlth, 155 Coll St, Toronto, ON M5T3M7, Canada
[11] Univ Melbourne, Genet Epidemiol Lab, Dept Pathol, Parkville, Vic 3010, Australia
[12] Mem Sloan Kettering Canc Ctr, 300 East 66th St, New York, NY 10065 USA
[13] C Anthony & Jean Whittingham Canc Ctr, 34 Maple St, Norwalk, CT 06856 USA
[14] Weill Cornell Med Breast Ctr, 428 E 72nd St, New York, NY 10021 USA
[15] Columbia Univ, Dept Pediat, 1150 St Nicholas Ave, New York, NY 10032 USA
[16] Columbia Univ, Dept Med, 1150 St Nicholas Ave, New York, NY 10032 USA
[17] Columbia Univ, Med Ctr, Herbert Irving Comprehens Canc Ctr, 1130 St Nicholas Ave, New York, NY 10032 USA
[18] Univ Melbourne, Dept Med, St Vincents Hosp, Parkville, Vic 3010, Australia
[19] St Vincents Hosp, Dept Med Oncol, 41 Victoria St, Fitzroy, Vic 3065, Australia
[20] Univ New South Wales, Prince Wales Clin Sch, Sydney, NSW 2052, Australia
[21] Prince Wales Hosp, Dept Med Oncol, Barker St, Randwick, NSW 2031, Australia
[22] Peter MacCallum Canc Ctr, Div Canc Med, 305 Grattan St, Melbourne, Vic 3000, Australia
[23] Peter MacCallum Canc Ctr, Melbourne, Vic 3000, Australia
[24] Univ Toronto, Dept Mol Genet, 164 Coll St, Toronto, ON M5S 3G9, Canada
[25] Univ Toronto, Dept Lab Med & Pathobiol, 164 Coll St, Toronto, ON M5S 3G9, Canada
[26] Univ Utah Hlth, Dept Med, 2000 Cir Hope Dr, Salt Lake City, UT 84103 USA
[27] Univ Utah Hlth, Huntsman Canc Inst, 2000 Cir Hope Dr, Salt Lake City, UT 84103 USA
[28] Fox Chase Canc Ctr, Dept Clin Genet, 333 Cottman Ave, Philadelphia, PA 19111 USA
基金
英国医学研究理事会; 美国国家卫生研究院; 欧盟地平线“2020”;
关键词
Breast cancer; Non-steroidal anti-inflammatory drugs; Family history; High-risk population; PRIMARY PREVENTION; COLORECTAL-CANCER; INFLAMMATORY-DRUGS; BOADICEA MODEL; MUTATION; DISEASE; OVARIAN; BRCA1; CHEMOPREVENTION; SUSCEPTIBILITY;
D O I
10.1186/s13058-019-1135-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundThe use of aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) has been associated with reduced breast cancer risk, but it is not known if this association extends to women at familial or genetic risk. We examined the association between regular NSAID use and breast cancer risk using a large cohort of women selected for breast cancer family history, including 1054 BRCA1 or BRCA2 mutation carriers.MethodsWe analyzed a prospective cohort (N=5606) and a larger combined, retrospective and prospective, cohort (N=8233) of women who were aged 18 to 79years, enrolled before June 30, 2011, with follow-up questionnaire data on medication history. The prospective cohort was further restricted to women without breast cancer when medication history was asked by questionnaire. Women were recruited from seven study centers in the United States, Canada, and Australia. Associations were estimated using multivariable Cox proportional hazards regression models adjusted for demographics, lifestyle factors, family history, and other medication use. Women were classified as regular or non-regular users of aspirin, COX-2 inhibitors, ibuprofen and other NSAIDs, and acetaminophen (control) based on self-report at follow-up of ever using the medication for at least twice a week for 1month prior to breast cancer diagnosis. The main outcome was incident invasive breast cancer, based on self- or relative-report (81% confirmed pathologically).ResultsFrom fully adjusted analyses, regular aspirin use was associated with a 39% and 37% reduced risk of breast cancer in the prospective (HR=0.61; 95% CI=0.33-1.14) and combined cohorts (HR=0.63; 95% CI=0.57-0.71), respectively. Regular use of COX-2 inhibitors was associated with a 61% and 71% reduced risk of breast cancer (prospective HR=0.39; 95% CI=0.15-0.97; combined HR=0.29; 95% CI=0.23-0.38). Other NSAIDs and acetaminophen were not associated with breast cancer risk in either cohort. Associations were not modified by familial risk, and consistent patterns were found by BRCA1 and BRCA2 carrier status, estrogen receptor status, and attained age.ConclusionRegular use of aspirin and COX-2 inhibitors might reduce breast cancer risk for women at familial or genetic risk.
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页数:13
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