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Progestin and estrogen potency of combination oral contraceptives and endometrial cancer risk.

Publication ,  Journal Article
Maxwell, GL; Schildkraut, JM; Calingaert, B; Risinger, JI; Dainty, L; Marchbanks, PA; Berchuck, A; Barrett, JC; Rodriguez, GC
Published in: Gynecol Oncol
November 2006

OBJECTIVE: Using data from a case-control study of endometrial cancer, we investigated the relationship between the progestin and estrogen potency in combination oral contraceptives (OCs) and the risk of developing endometrial cancer. METHODS: Subjects included 434 endometrial cancer cases and 2,557 controls identified from the Cancer and Steroid Hormone (CASH) study. OCs were classified into four categories according to the individual potencies of each hormonal constituent (high versus low estrogen or progestin potency). Logistic regression was used to evaluate associations between endometrial cancer risk and combination OC formulations. RESULTS: With non-users as the referent group, use of OCs with either high potency progestin [odds ratio for endometrial cancer (OR)=0.21, 95% confidence interval (CI)=0.10 to 0.43] or with low potency progestin (OR=0.39, 95% CI=0.25 to 0.60) were both associated with a decreased risk of endometrial cancer. Overall high progestin potency OCs did not confer significantly more protection than low progestin potency OCs (OR=0.52, 95% CI=0.24 to 1.14). However, among women with a body mass index of 22.1 kg/m2 or higher, those who used high progestin potency oral contraceptives had a lower risk of endometrial cancer than those who used low progestin potency oral contraceptives (OR=0.31, 95% CI=0.11 to 0.92) while those with a BMI below 22.1 kg/m2 did not (OR=1.36, 95% CI=0.39 to 4.70). CONCLUSION: The potency of the progestin in most OCs appears adequate to provide a protective effect against endometrial cancer. Higher progestin-potency OCs may be more protective than lower progestin potency OCs among women with a larger body habitus.

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Published In

Gynecol Oncol

DOI

ISSN

0090-8258

Publication Date

November 2006

Volume

103

Issue

2

Start / End Page

535 / 540

Location

United States

Related Subject Headings

  • SEER Program
  • Progestins
  • Oncology & Carcinogenesis
  • Middle Aged
  • Logistic Models
  • Humans
  • Female
  • Estrogens
  • Endometrial Neoplasms
  • Contraceptives, Oral, Hormonal
 

Citation

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Maxwell, G. L., Schildkraut, J. M., Calingaert, B., Risinger, J. I., Dainty, L., Marchbanks, P. A., … Rodriguez, G. C. (2006). Progestin and estrogen potency of combination oral contraceptives and endometrial cancer risk. Gynecol Oncol, 103(2), 535–540. https://doi.org/10.1016/j.ygyno.2006.03.046
Maxwell, G. L., J. M. Schildkraut, B. Calingaert, J. I. Risinger, L. Dainty, P. A. Marchbanks, A. Berchuck, J. C. Barrett, and G. C. Rodriguez. “Progestin and estrogen potency of combination oral contraceptives and endometrial cancer risk.Gynecol Oncol 103, no. 2 (November 2006): 535–40. https://doi.org/10.1016/j.ygyno.2006.03.046.
Maxwell GL, Schildkraut JM, Calingaert B, Risinger JI, Dainty L, Marchbanks PA, et al. Progestin and estrogen potency of combination oral contraceptives and endometrial cancer risk. Gynecol Oncol. 2006 Nov;103(2):535–40.
Maxwell, G. L., et al. “Progestin and estrogen potency of combination oral contraceptives and endometrial cancer risk.Gynecol Oncol, vol. 103, no. 2, Nov. 2006, pp. 535–40. Pubmed, doi:10.1016/j.ygyno.2006.03.046.
Maxwell GL, Schildkraut JM, Calingaert B, Risinger JI, Dainty L, Marchbanks PA, Berchuck A, Barrett JC, Rodriguez GC. Progestin and estrogen potency of combination oral contraceptives and endometrial cancer risk. Gynecol Oncol. 2006 Nov;103(2):535–540.
Journal cover image

Published In

Gynecol Oncol

DOI

ISSN

0090-8258

Publication Date

November 2006

Volume

103

Issue

2

Start / End Page

535 / 540

Location

United States

Related Subject Headings

  • SEER Program
  • Progestins
  • Oncology & Carcinogenesis
  • Middle Aged
  • Logistic Models
  • Humans
  • Female
  • Estrogens
  • Endometrial Neoplasms
  • Contraceptives, Oral, Hormonal