TY - JOUR
T1 - Cancer Incidence in a Cohort of Infertile Women
AU - Modan, Baruch
AU - Ron, Elaine
AU - Lerner-Geva, Liat
AU - Blumstein, Tzvia
AU - Menczer, Joseph
AU - Rabinovici, Jaron
AU - Oelsner, Gabriel
AU - Freedman, Laurence
AU - Mashiach, Shlomo
AU - Lunenfeld, Bruno
PY - 1998/6/1
Y1 - 1998/6/1
N2 - Among 2,496 infertile Israeli women treated between 1964 and 1974, 143 cancer cases were observed as compared with 116.1 expected (standardized incidence ratio (SIR) = 1.2, 95% confidence interval (CI) 1.0-1.5) through 1991. Site-specific analysis revealed 12 ovarian cancers versus 7.2 expected (SIR = 1.6, 95% CI 0.8-2.9), 21 endometrial cancers versus 4.3 expected (SIR = 4.85, 95% CI 3.0-7.4), and 59 breast cancers versus 46.6 expected (SIR = 1.3, 95% CI 0.96-1.6). Sensitivity analysis revealed that confounding was unlikely to explain the raised risk of endometrial cancer, but nulliparity might explain the increased risk of ovarian cancer. The excess of endometrial cancer was prominent among patients with normal estrogen production but progesterone deficiency (SIR = 9.4, 95% CI 5.0-16.0). The risk for ovarian cancer was similar among the total groups of treated and untreated patients (SIR = 1.7 vs. 1.6). The standardized incidence ratio for endometrial cancer was higher among the treated group than the untreated group, although not significantly. Treatment with ovulation-inducing drugs does not appear to increase the risk for ovarian cancer, but its role cannot be completely excluded.
AB - Among 2,496 infertile Israeli women treated between 1964 and 1974, 143 cancer cases were observed as compared with 116.1 expected (standardized incidence ratio (SIR) = 1.2, 95% confidence interval (CI) 1.0-1.5) through 1991. Site-specific analysis revealed 12 ovarian cancers versus 7.2 expected (SIR = 1.6, 95% CI 0.8-2.9), 21 endometrial cancers versus 4.3 expected (SIR = 4.85, 95% CI 3.0-7.4), and 59 breast cancers versus 46.6 expected (SIR = 1.3, 95% CI 0.96-1.6). Sensitivity analysis revealed that confounding was unlikely to explain the raised risk of endometrial cancer, but nulliparity might explain the increased risk of ovarian cancer. The excess of endometrial cancer was prominent among patients with normal estrogen production but progesterone deficiency (SIR = 9.4, 95% CI 5.0-16.0). The risk for ovarian cancer was similar among the total groups of treated and untreated patients (SIR = 1.7 vs. 1.6). The standardized incidence ratio for endometrial cancer was higher among the treated group than the untreated group, although not significantly. Treatment with ovulation-inducing drugs does not appear to increase the risk for ovarian cancer, but its role cannot be completely excluded.
KW - Breast neoplasms
KW - Endometrial neoplasms
KW - Infertility
KW - Ovarian neoplasms
KW - Ovulation induction
UR - http://www.scopus.com/inward/record.url?scp=0032102946&partnerID=8YFLogxK
U2 - 10.1093/oxfordjournals.aje.a009397
DO - 10.1093/oxfordjournals.aje.a009397
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C2 - 9620047
AN - SCOPUS:0032102946
SN - 0002-9262
VL - 147
SP - 1038
EP - 1042
JO - American Journal of Epidemiology
JF - American Journal of Epidemiology
IS - 11
ER -