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. Author manuscript; available in PMC: 2014 Jul 22.
Published in final edited form as: Semin Reprod Med. 2012 Apr 27;30(2):131–145. doi: 10.1055/s-0032-1307421

Table 4.

Findings from Cohort Studies Regarding the Relationship of Fertility Drug Use to Uterine Cancer Risk

Study Primary Exposure
of Interest
No. of
Cancers
in Exposed
No. of
Cancers in
Unexposed
SIR in Exposed
(95% CI)
SIR in Unexposed
(95% CI)
RR (Exposed versus
Unexposed)
Comments
Venn et aI48 IVF treatment 2 3 2.22 (0.55–0.87) 3.48(1.12–10.8) 0.65 (0.11–3.94) Registry match
Venn et al18 IVF treatment 5 7 1.09(0.45–2.61) 2.47 (1.18–5.18) Registry match; no RR reported
Doyle et al53 Ovarian stimulation treatments 3 1 1.21 (0.25–3.53) 1.68(0.04–9.37) 0.72 (0.06–8.62)
Althuis et al101 Clomiphene 19 20 2.14(1.3–3.3) 1.24(0.8–1.9) 1.79(0.9–3.4) Somewhat higher risks for women using higher dosages, with extended follow-up, and who remained nulligravid
Dor et al14 IVF treatment 2 2.25 (0.25–8.11) Registry match; no untreated group
Calderon-Margalit et al49 Self-reported exposure to ovulation induction drugs 5 39 3.32 (1.31–8.42) Restricted to parous women
dos Santos Silva et al52 Ovarian stimulation treatments 18 12 2.31 (1.37–3.64) 1.66(0.86–2.90) 1.39(0.63–3.16) Women given 2250+ mg of clomiphene had a RR of 2.62 (0.94–6.82)
Jensen et al102 Clomiphene 29 54 1.36(0.83–2.23) Higher risks for those with 6+ cycles. Also elevated RR for those exposed for multiple cycles to gonadotropins or hCG

SIR, standardized incidence ratio; CI, confidence interval; RR, relative risk; IVF, in vitro fertilization; hCG, human chorionic gonadotropin.