TY - JOUR
T1 - Predicting circulating CA125 levels among healthy premenopausal women
AU - Sasamoto, Naoko
AU - Babic, Ana
AU - Rosner, Bernard A.
AU - Fortner, Renee T.
AU - Vitonis, Allison F.
AU - Yamamoto, Hidemi
AU - Fichorova, Raina N.
AU - Tjønneland, Anne
AU - Hansen, Louise
AU - Overvad, Kim
AU - Kvaskoff, Marina
AU - Fournier, Agnes
AU - Mancini, Francesca Romana
AU - Boeing, Heiner
AU - Trichopoulou, Antonia
AU - Peppa, Eleni
AU - Karakatsani, Anna
AU - Palli, Domenico
AU - Pala, Valeria
AU - Mattiello, Amalia
AU - Tumino, Rosario
AU - Grasso, Chiara C.
AU - Onland-Moret, N. Charlotte
AU - Weiderpass, Elisabete
AU - Quiros, J. Ramon
AU - Lujan-Barroso, Leila
AU - Rodríguez-Barranco, Miguel
AU - Colorado-Yohar, Sandra
AU - Barricarte, Aurelio
AU - Dorronsoro, Miren
AU - Idahl, Annika
AU - Lundin, Eva
AU - Sartor, Hanna
AU - Khaw, Kay Tee
AU - Key, Timothy J.
AU - Muller, David
AU - Riboli, Elio
AU - Gunter, Marc J.
AU - Dossus, Laure
AU - Kaaks, Rudolf
AU - Cramer, Daniel W.
AU - Tworoger, Shelley S.
AU - Terry, Kathryn L.
PY - 2019
Y1 - 2019
N2 - Background: Cancer antigen 125 (CA125) is the most promising ovarian cancer screening biomarker to date. Multiple studies reported CA125 levels vary by personal characteristics, which could inform personalized CA125 thresholds. However, this has not been well described in premenopausal women. Methods: We evaluated predictors of CA125 levels among 815 premenopausal women from the New England Case Control Study (NEC). We developed linear and dichotomous (-35 U/mL) CA125 prediction models and externally validated an abridged model restricting to available predictors among 473 premenopausal women in the European Prospective Investigation into Cancer and Nutrition Study (EPIC). Results: The final linear CA125 prediction model included age, race, tubal ligation, endometriosis, menstrual phase at blood draw, and fibroids, which explained 7% of the total variance of CA125. The correlation between observed and predicted CA125 levels based on the abridged model (including age, race, and menstrual phase at blood draw) had similar correlation coefficients in NEC (r = 0.22) and in EPIC (r= 0.22). The dichotomous CA125 prediction model included age, tubal ligation, endometriosis, prior personal cancer diagnosis, family history of ovarian cancer, number of miscarriages, menstrual phase at blood draw, and smoking status with AUC of 0.83. The abridged dichotomous model (including age, number of miscarriages, menstrual phase at blood draw, and smoking status) showed similar AUCs in NEC (0.73) and in EPIC (0.78). Conclusions: We identified a combination of factors associated with CA125 levels in premenopausal women. Impact: Our model could be valuable in identifying healthy women likely to have elevated CA125 and consequently improve its specificity for ovarian cancer screening.
AB - Background: Cancer antigen 125 (CA125) is the most promising ovarian cancer screening biomarker to date. Multiple studies reported CA125 levels vary by personal characteristics, which could inform personalized CA125 thresholds. However, this has not been well described in premenopausal women. Methods: We evaluated predictors of CA125 levels among 815 premenopausal women from the New England Case Control Study (NEC). We developed linear and dichotomous (-35 U/mL) CA125 prediction models and externally validated an abridged model restricting to available predictors among 473 premenopausal women in the European Prospective Investigation into Cancer and Nutrition Study (EPIC). Results: The final linear CA125 prediction model included age, race, tubal ligation, endometriosis, menstrual phase at blood draw, and fibroids, which explained 7% of the total variance of CA125. The correlation between observed and predicted CA125 levels based on the abridged model (including age, race, and menstrual phase at blood draw) had similar correlation coefficients in NEC (r = 0.22) and in EPIC (r= 0.22). The dichotomous CA125 prediction model included age, tubal ligation, endometriosis, prior personal cancer diagnosis, family history of ovarian cancer, number of miscarriages, menstrual phase at blood draw, and smoking status with AUC of 0.83. The abridged dichotomous model (including age, number of miscarriages, menstrual phase at blood draw, and smoking status) showed similar AUCs in NEC (0.73) and in EPIC (0.78). Conclusions: We identified a combination of factors associated with CA125 levels in premenopausal women. Impact: Our model could be valuable in identifying healthy women likely to have elevated CA125 and consequently improve its specificity for ovarian cancer screening.
U2 - 10.1158/1055-9965.EPI-18-1120
DO - 10.1158/1055-9965.EPI-18-1120
M3 - Article
C2 - 30948451
AN - SCOPUS:85067215131
SN - 1055-9965
VL - 28
SP - 1076
EP - 1085
JO - Cancer Epidemiology Biomarkers and Prevention
JF - Cancer Epidemiology Biomarkers and Prevention
IS - 6
ER -