Benign and Malignant Outcomes in the Offspring of Females Exposed In Utero to Diethylstilbestrol (DES): An Update from the NCI Third Generation Study

Author:

Titus Linda1,Hatch Elizabeth E.2,Bertrand Kimberly A.3,Palmer Julie R.3,Strohsnitter William C.4,Huo Dezheng5,Curry Michael6ORCID,Hyer Marianne6ORCID,Aagaard Kjersti7,Gierach Gretchen L.8ORCID,Troisi Rebecca8

Affiliation:

1. Department of Pediatrics, Geisel School of Medicine at Dartmouth, and the Norris Cotton Cancer Center, Lebanon, NH 03756, USA

2. Department of Epidemiology and Biostatistics, Boston University School of Public Health, Boston, MA 02118, USA

3. Boston University Chobanian & Avedisian School of Medicine and Slone Epidemiology Center, Boston University, Boston, MA 02118, USA

4. Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01655, USA

5. Department of Public Health Sciences, University of Chicago, Chicago, IL 60637, USA

6. Information Management Services, Rockville, MD 20852, USA

7. Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine, Baylor College of Medicine and Texas Children’s Hospital, Houston, TX 77401, USA

8. Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892, USA

Abstract

Background: Females exposed prenatally to diethylstilbestrol (DES) have an elevated risk of cervical dysplasia, breast cancer, and clear cell adenocarcinoma (CCA) of the cervix/vagina. Testicular cancer risk is increased in prenatally exposed males. Epigenetic changes may mediate the transmission of DES effects to the next (“third”) generation of offspring. Methods: Using data self-reported by third-generation females, we assessed DES in relation to the risk of cancer and benign breast and reproductive tract conditions. Using data from prenatally DES-exposed and unexposed mothers, we assessed DES in relation to cancer risk in their female and male offspring. Cancer risk was assessed by standardized incidence ratios (SIR) and 95% confidence intervals (CI); the risks of benign and malignant diagnoses were assessed by hazard ratios (HR) and 95% CI. Results: In self-reported data, DES exposure was not associated with an increased risk of overall cancer (HR 0.83; CI 0.36–1.90), breast cancer, or severe cervical dysplasia. No females reported CCA. The risk of borderline ovarian cancer appeared elevated, but the HR was imprecise (3.46; CI 0.37–32.42). Based on mothers’ reports, DES exposure did not increase the risk of overall cancer (HR 0.80; CI 0.49–1.32) or of other cancers in third-generation females. Overall cancer risk in exposed males appeared elevated (HR 1.41; CI 0.70–2.86), but the CI was wide. The risk of testicular cancer was not elevated in exposed males; no cases of prostate cancer were reported. Conclusions: To date, there is little evidence that DES is associated with cancer risk in third-generation females or males, but these individuals are relatively young, and further follow-up is needed.

Funder

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health

Publisher

MDPI AG

Reference33 articles.

1. Does the administration of diethylstilbestrol during pregnancy have therapeutic value?;Dieckmann;Am. J. Obstet. Gynecol.,1953

2. Effect of stilbestrol on pregnancy compared to the effect of a placebo;Ferguson;Am. J. Obstet. Gynecol.,1953

3. (1972). Selected item from the FDA drug bulletin-November 1971: Diethylstilbestrol contraindicated in pregnancy. Calif. Med., 116, 85–86.

4. Adenocarcinoma of the vagina: Association of maternal stilbestrol therapy with tumor appearance in young women;Herbst;N. Engl. J. Med.,1971

5. Cancer risk in women exposed to diethylstilbestrol in utero;Hatch;JAMA,1998

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