TY - JOUR
T1 - Menstrual Factors, Reproductive History, Hormone Use, and Urothelial Carcinoma Risk
T2 - A Prospective Study in the EPIC Cohort
AU - Lujan-Barroso, Leila
AU - Botteri, Edoardo
AU - Caini, Saverio
AU - Ljungberg, Börje
AU - Roswall, Nina
AU - Tjønneland, Anne
AU - Bueno-de-Mesquita, Bas
AU - Gram, Inger T.
AU - Tumino, Rosario
AU - Kiemeney, Lambertus A.
AU - Liedberg, Fredrik
AU - Stocks, Tanja
AU - Gunter, Marc J.
AU - Murphy, Neil
AU - Cervenka, Iris
AU - Fournier, Agnès
AU - Kvaskoff, Marina
AU - Häggström, Christel
AU - Overvad, Kim
AU - Lund, Eiliv
AU - Waaseth, Marit
AU - Fortner, Renée Turzanski
AU - Kühn, Tilman
AU - Menéndez, Virginia
AU - Sánchez, Maria Jose
AU - Santiuste, Carmen
AU - Perez-Cornago, Aurora
AU - Zamora-Ros, Raul
AU - Cross, Amanda J.
AU - Trichopoulou, Antonia
AU - Karakatsani, Anna
AU - Peppa, Eleni
AU - Palli, Domenico
AU - Krogh, Vittorio
AU - Sciannameo, Veronica
AU - Mattiello, Amalia
AU - Panico, Salvatore
AU - van Gils, Carla H.
AU - Onland-Moret, N. Charlotte
AU - Barricarte, Aurelio
AU - Amiano, Pilar
AU - Khaw, Kay Tee
AU - Boeing, Heiner
AU - Weiderpass, Elisabete
AU - Duell, Eric J.
PY - 2020
Y1 - 2020
N2 - BACKGROUND: Urothelial carcinoma is the predominant (95%) bladder cancer subtype in industrialized nations. Animal and epidemiologic human studies suggest that hormonal factors may influence urothelial carcinoma risk. METHODS: We used an analytic cohort of 333,919 women from the European Prospective Investigation into Cancer and Nutrition Cohort. Associations between hormonal factors and incident urothelial carcinoma (overall and by tumor grade, tumor aggressiveness, and non-muscle-invasive urothelial carcinoma) risk were evaluated using Cox proportional hazards models. RESULTS: During a mean of 15 years of follow-up, 529 women developed urothelial carcinoma. In a model including number of full-term pregnancies (FTP), menopausal status, and menopausal hormone therapy (MHT), number of FTP was inversely associated with urothelial carcinoma risk (HR≥5vs1 = 0.48; 0.25-0.90; Ptrend in parous women = 0.010) and MHT use (compared with nonuse) was positively associated with urothelial carcinoma risk (HR = 1.27; 1.03-1.57), but no dose response by years of MHT use was observed. No modification of HRs by smoking status was observed. Finally, sensitivity analyses in never smokers showed similar HR patterns for the number of FTP, while no association between MHT use and urothelial carcinoma risk was observed. Association between MHT use and urothelial carcinoma risk remained significant only in current smokers. No heterogeneity of the risk estimations in the final model was observed by tumor aggressiveness or by tumor grade. A positive association between MTH use and non-muscle-invasive urothelial carcinoma risk was observed. CONCLUSIONS: Our results support that increasing the number of FTP may reduce urothelial carcinoma risk. IMPACT: More detailed studies on parity are needed to understand the possible effects of perinatal hormone changes in urothelial cells.
AB - BACKGROUND: Urothelial carcinoma is the predominant (95%) bladder cancer subtype in industrialized nations. Animal and epidemiologic human studies suggest that hormonal factors may influence urothelial carcinoma risk. METHODS: We used an analytic cohort of 333,919 women from the European Prospective Investigation into Cancer and Nutrition Cohort. Associations between hormonal factors and incident urothelial carcinoma (overall and by tumor grade, tumor aggressiveness, and non-muscle-invasive urothelial carcinoma) risk were evaluated using Cox proportional hazards models. RESULTS: During a mean of 15 years of follow-up, 529 women developed urothelial carcinoma. In a model including number of full-term pregnancies (FTP), menopausal status, and menopausal hormone therapy (MHT), number of FTP was inversely associated with urothelial carcinoma risk (HR≥5vs1 = 0.48; 0.25-0.90; Ptrend in parous women = 0.010) and MHT use (compared with nonuse) was positively associated with urothelial carcinoma risk (HR = 1.27; 1.03-1.57), but no dose response by years of MHT use was observed. No modification of HRs by smoking status was observed. Finally, sensitivity analyses in never smokers showed similar HR patterns for the number of FTP, while no association between MHT use and urothelial carcinoma risk was observed. Association between MHT use and urothelial carcinoma risk remained significant only in current smokers. No heterogeneity of the risk estimations in the final model was observed by tumor aggressiveness or by tumor grade. A positive association between MTH use and non-muscle-invasive urothelial carcinoma risk was observed. CONCLUSIONS: Our results support that increasing the number of FTP may reduce urothelial carcinoma risk. IMPACT: More detailed studies on parity are needed to understand the possible effects of perinatal hormone changes in urothelial cells.
U2 - 10.1158/1055-9965.EPI-20-0184
DO - 10.1158/1055-9965.EPI-20-0184
M3 - Article
C2 - 32467345
AN - SCOPUS:85089126979
SN - 1538-7755
VL - 29
SP - 1654
EP - 1664
JO - Cancer Epidemiology Biomarkers and Prevention
JF - Cancer Epidemiology Biomarkers and Prevention
IS - 8
ER -