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Constitutively active ESR1 mutations in gynecologic malignancies and clinical response to estrogen-receptor directed therapies.

Publication ,  Journal Article
Gaillard, SL; Andreano, KJ; Gay, LM; Steiner, M; Jorgensen, MS; Davidson, BA; Havrilesky, LJ; Alvarez Secord, A; Valea, FA; Colon-Otero, G ...
Published in: Gynecol Oncol
July 2019

OBJECTIVE: Endocrine therapy is often considered as a treatment for hormone-responsive gynecologic malignancies. In breast cancer, activating mutations in the estrogen receptor (mutESR1) contribute to therapeutic resistance to endocrine therapy, especially aromatase inhibitors (AIs). The purpose of this study was to evaluate the frequency and clinical relevance of ESR1 genomic alterations in gynecologic malignancies. METHODS: DNA from FFPE tumor tissue obtained during routine clinical care for 9645 gynecologic malignancies (ovary, fallopian tube, uterus, cervix, vagina, vulvar, and placenta) was analyzed for all classes of genomic alterations (base substitutions (muts), insertions, deletions, rearrangements, and amplifications) in ESR1 by hybrid capture next generation sequencing. A subset of alterations was characterized in laboratory-based transcription assays for response to endocrine therapies. RESULTS: A total of 295 ESR1 genomic alterations were identified in 285 (3.0%) cases. mutESR1 were present in 86 (0.9%) cases and were more common in uterine compared to other cancers (2.0% vs <1%, respectively p < 0.001). mutESR1 were enriched in carcinomas with endometrioid versus serous histology (4.4% vs 0.2% respectively, p < 0.0001 in uterine and 3.5% vs 0.3% respectively, p = 0.0004 in ovarian carcinomas). In three of four patients with serial sampling, mutESR1 emerged under the selective pressure of AI therapy. Despite decreased potency of estrogen receptor (ER) antagonists in transcriptional assays, clinical benefit was observed following treatment with selective ER-targeted therapy, in one case lasting >48 months. CONCLUSIONS: While the prevalence of ESR1 mutations in gynecologic malignancies is low, there are significant clinical implications useful in guiding therapeutic approaches for these cancers.

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Published In

Gynecol Oncol

DOI

EISSN

1095-6859

Publication Date

July 2019

Volume

154

Issue

1

Start / End Page

199 / 206

Location

United States

Related Subject Headings

  • Young Adult
  • Treatment Outcome
  • Transcriptome
  • Transcription, Genetic
  • Selective Estrogen Receptor Modulators
  • Oncology & Carcinogenesis
  • Mutation
  • Molecular Targeted Therapy
  • Middle Aged
  • Humans
 

Citation

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Gaillard, S. L., Andreano, K. J., Gay, L. M., Steiner, M., Jorgensen, M. S., Davidson, B. A., … Elvin, J. A. (2019). Constitutively active ESR1 mutations in gynecologic malignancies and clinical response to estrogen-receptor directed therapies. Gynecol Oncol, 154(1), 199–206. https://doi.org/10.1016/j.ygyno.2019.04.010
Gaillard, Stéphanie L., Kaitlyn J. Andreano, Laurie M. Gay, Meghan Steiner, Matthew S. Jorgensen, Brittany Anne Davidson, Laura J. Havrilesky, et al. “Constitutively active ESR1 mutations in gynecologic malignancies and clinical response to estrogen-receptor directed therapies.Gynecol Oncol 154, no. 1 (July 2019): 199–206. https://doi.org/10.1016/j.ygyno.2019.04.010.
Gaillard SL, Andreano KJ, Gay LM, Steiner M, Jorgensen MS, Davidson BA, et al. Constitutively active ESR1 mutations in gynecologic malignancies and clinical response to estrogen-receptor directed therapies. Gynecol Oncol. 2019 Jul;154(1):199–206.
Gaillard, Stéphanie L., et al. “Constitutively active ESR1 mutations in gynecologic malignancies and clinical response to estrogen-receptor directed therapies.Gynecol Oncol, vol. 154, no. 1, July 2019, pp. 199–206. Pubmed, doi:10.1016/j.ygyno.2019.04.010.
Gaillard SL, Andreano KJ, Gay LM, Steiner M, Jorgensen MS, Davidson BA, Havrilesky LJ, Alvarez Secord A, Valea FA, Colon-Otero G, Zajchowski DA, Chang C-Y, McDonnell DP, Berchuck A, Elvin JA. Constitutively active ESR1 mutations in gynecologic malignancies and clinical response to estrogen-receptor directed therapies. Gynecol Oncol. 2019 Jul;154(1):199–206.
Journal cover image

Published In

Gynecol Oncol

DOI

EISSN

1095-6859

Publication Date

July 2019

Volume

154

Issue

1

Start / End Page

199 / 206

Location

United States

Related Subject Headings

  • Young Adult
  • Treatment Outcome
  • Transcriptome
  • Transcription, Genetic
  • Selective Estrogen Receptor Modulators
  • Oncology & Carcinogenesis
  • Mutation
  • Molecular Targeted Therapy
  • Middle Aged
  • Humans