Cargando…

Association of PET-based estradiol-challenge test for breast cancer progesterone receptors with response to endocrine therapy

Estrogen receptor (ER) testing of breast cancer imperfectly predicts response to endocrine therapy (ET). We hypothesize that a brief estradiol challenge will increase tumor progesterone receptor (PgR) levels only in tumors with functional ER. In this prospective, phase 2, single-center, single-arm t...

Descripción completa

Detalles Bibliográficos
Autores principales: Dehdashti, Farrokh, Wu, Ningying, Ma, Cynthia X., Naughton, Michael J., Katzenellenbogen, John A., Siegel, Barry A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854611/
https://www.ncbi.nlm.nih.gov/pubmed/33531464
http://dx.doi.org/10.1038/s41467-020-20814-9
_version_ 1783646116384866304
author Dehdashti, Farrokh
Wu, Ningying
Ma, Cynthia X.
Naughton, Michael J.
Katzenellenbogen, John A.
Siegel, Barry A.
author_facet Dehdashti, Farrokh
Wu, Ningying
Ma, Cynthia X.
Naughton, Michael J.
Katzenellenbogen, John A.
Siegel, Barry A.
author_sort Dehdashti, Farrokh
collection PubMed
description Estrogen receptor (ER) testing of breast cancer imperfectly predicts response to endocrine therapy (ET). We hypothesize that a brief estradiol challenge will increase tumor progesterone receptor (PgR) levels only in tumors with functional ER. In this prospective, phase 2, single-center, single-arm trial (NCT02455453), we report the association of response to ET with change in tumor uptake of the progestin analog, 21-[(18)F]fluorofuranylnorprogesterone (FFNP), before and after a one-day estradiol challenge. In 43 postmenopausal women with advanced ER+ breast cancer, we show a post-challenge increase in tumor FFNP uptake only in 28 subjects with clinical benefit from ET (responders), but not in 15 without clinical benefit (nonresponders) (p < 0.0001), indicating 100% sensitivity and specificity. We further show significantly longer survival (p < 0.0001) in the responding subjects. Our results demonstrate that change in tumor FFNP uptake after estradiol challenge is highly predictive of response to ET in women with ER+ breast cancer.
format Online
Article
Text
id pubmed-7854611
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-78546112021-02-11 Association of PET-based estradiol-challenge test for breast cancer progesterone receptors with response to endocrine therapy Dehdashti, Farrokh Wu, Ningying Ma, Cynthia X. Naughton, Michael J. Katzenellenbogen, John A. Siegel, Barry A. Nat Commun Article Estrogen receptor (ER) testing of breast cancer imperfectly predicts response to endocrine therapy (ET). We hypothesize that a brief estradiol challenge will increase tumor progesterone receptor (PgR) levels only in tumors with functional ER. In this prospective, phase 2, single-center, single-arm trial (NCT02455453), we report the association of response to ET with change in tumor uptake of the progestin analog, 21-[(18)F]fluorofuranylnorprogesterone (FFNP), before and after a one-day estradiol challenge. In 43 postmenopausal women with advanced ER+ breast cancer, we show a post-challenge increase in tumor FFNP uptake only in 28 subjects with clinical benefit from ET (responders), but not in 15 without clinical benefit (nonresponders) (p < 0.0001), indicating 100% sensitivity and specificity. We further show significantly longer survival (p < 0.0001) in the responding subjects. Our results demonstrate that change in tumor FFNP uptake after estradiol challenge is highly predictive of response to ET in women with ER+ breast cancer. Nature Publishing Group UK 2021-02-02 /pmc/articles/PMC7854611/ /pubmed/33531464 http://dx.doi.org/10.1038/s41467-020-20814-9 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Dehdashti, Farrokh
Wu, Ningying
Ma, Cynthia X.
Naughton, Michael J.
Katzenellenbogen, John A.
Siegel, Barry A.
Association of PET-based estradiol-challenge test for breast cancer progesterone receptors with response to endocrine therapy
title Association of PET-based estradiol-challenge test for breast cancer progesterone receptors with response to endocrine therapy
title_full Association of PET-based estradiol-challenge test for breast cancer progesterone receptors with response to endocrine therapy
title_fullStr Association of PET-based estradiol-challenge test for breast cancer progesterone receptors with response to endocrine therapy
title_full_unstemmed Association of PET-based estradiol-challenge test for breast cancer progesterone receptors with response to endocrine therapy
title_short Association of PET-based estradiol-challenge test for breast cancer progesterone receptors with response to endocrine therapy
title_sort association of pet-based estradiol-challenge test for breast cancer progesterone receptors with response to endocrine therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854611/
https://www.ncbi.nlm.nih.gov/pubmed/33531464
http://dx.doi.org/10.1038/s41467-020-20814-9
work_keys_str_mv AT dehdashtifarrokh associationofpetbasedestradiolchallengetestforbreastcancerprogesteronereceptorswithresponsetoendocrinetherapy
AT wuningying associationofpetbasedestradiolchallengetestforbreastcancerprogesteronereceptorswithresponsetoendocrinetherapy
AT macynthiax associationofpetbasedestradiolchallengetestforbreastcancerprogesteronereceptorswithresponsetoendocrinetherapy
AT naughtonmichaelj associationofpetbasedestradiolchallengetestforbreastcancerprogesteronereceptorswithresponsetoendocrinetherapy
AT katzenellenbogenjohna associationofpetbasedestradiolchallengetestforbreastcancerprogesteronereceptorswithresponsetoendocrinetherapy
AT siegelbarrya associationofpetbasedestradiolchallengetestforbreastcancerprogesteronereceptorswithresponsetoendocrinetherapy