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Association of progesterone receptor status with 21-gene recurrence score and survival among patients with estrogen receptor-positive breast cancer

BACKGROUND: Progesterone receptor (PR)-negative tumors have been shown to have worse prognosis and were underrepresented in recent trials on patients with estrogen receptor (ER)-positive breast cancer. The role of PR-negative status in the context of 21-gene recurrence score (RS) and nodal staging r...

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Autores principales: Ma, Sung Jun, Gill, Jasmin, Yendamuri, Keerti, Chatterjee, Udit, Waldman, Olivia, Dunne-Jaffe, Cynthia, Fekrmandi, Fatemeh, Shekher, Rohil, Iovoli, Austin, Yao, Song, Oladeru, Oluwadamilola T., Singh, Anurag K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10088125/
https://www.ncbi.nlm.nih.gov/pubmed/37041481
http://dx.doi.org/10.1186/s12885-023-10796-4
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author Ma, Sung Jun
Gill, Jasmin
Yendamuri, Keerti
Chatterjee, Udit
Waldman, Olivia
Dunne-Jaffe, Cynthia
Fekrmandi, Fatemeh
Shekher, Rohil
Iovoli, Austin
Yao, Song
Oladeru, Oluwadamilola T.
Singh, Anurag K.
author_facet Ma, Sung Jun
Gill, Jasmin
Yendamuri, Keerti
Chatterjee, Udit
Waldman, Olivia
Dunne-Jaffe, Cynthia
Fekrmandi, Fatemeh
Shekher, Rohil
Iovoli, Austin
Yao, Song
Oladeru, Oluwadamilola T.
Singh, Anurag K.
author_sort Ma, Sung Jun
collection PubMed
description BACKGROUND: Progesterone receptor (PR)-negative tumors have been shown to have worse prognosis and were underrepresented in recent trials on patients with estrogen receptor (ER)-positive breast cancer. The role of PR-negative status in the context of 21-gene recurrence score (RS) and nodal staging remains unclear. METHODS: The National Cancer Database (NCDB) was queried for women diagnosed between 2010 and 2017 with ER-positive, human epidermal growth factor receptor 2 (HER2)-negative, pT1-3N0-1a breast cancer. Logistic and Cox multivariable analyses (MVA) were performed to identify association of PR status with high RS (> 25) and overall survival (OS), respectively. RESULTS: Among 143,828 women, 130,349 (90.6%) and 13,479 (9.4%) patients had PR-positive and PR-negative tumors, respectively. Logistic MVA showed that PR-negative status was associated with higher RS (> 25: aOR 16.15, 95% CI 15.23–17.13). Cox MVA showed that PR-negative status was associated with worse OS (adjusted hazards ratio [aHR] 1.20, 95% CI 1.10–1.31). There was an interaction with nodal staging and chemotherapy (p = 0.049). Subgroup analyses using Cox MVA showed the magnitude of the chemotherapy benefit was greater among those with pN1a, PR-negative tumors than pN1a, PR-positive tumors (PR-positive: aHR 0.57, 95% CI 0.47–0.67; PR-negative: aHR 0.31, 95% CI 0.20–0.47). It was comparable among those with pN0 tumors regardless of PR status (PR-positive: aHR 0.74, 95% CI 0.66–0.82; PR-negative: aHR 0.63, 95% CI 0.51–0.77). CONCLUSION: PR-negative tumors were independently correlated with higher RS and were associated with greater OS benefits from chemotherapy for pN1a tumors, but not pN0 tumors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-10796-4.
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spelling pubmed-100881252023-04-12 Association of progesterone receptor status with 21-gene recurrence score and survival among patients with estrogen receptor-positive breast cancer Ma, Sung Jun Gill, Jasmin Yendamuri, Keerti Chatterjee, Udit Waldman, Olivia Dunne-Jaffe, Cynthia Fekrmandi, Fatemeh Shekher, Rohil Iovoli, Austin Yao, Song Oladeru, Oluwadamilola T. Singh, Anurag K. BMC Cancer Research BACKGROUND: Progesterone receptor (PR)-negative tumors have been shown to have worse prognosis and were underrepresented in recent trials on patients with estrogen receptor (ER)-positive breast cancer. The role of PR-negative status in the context of 21-gene recurrence score (RS) and nodal staging remains unclear. METHODS: The National Cancer Database (NCDB) was queried for women diagnosed between 2010 and 2017 with ER-positive, human epidermal growth factor receptor 2 (HER2)-negative, pT1-3N0-1a breast cancer. Logistic and Cox multivariable analyses (MVA) were performed to identify association of PR status with high RS (> 25) and overall survival (OS), respectively. RESULTS: Among 143,828 women, 130,349 (90.6%) and 13,479 (9.4%) patients had PR-positive and PR-negative tumors, respectively. Logistic MVA showed that PR-negative status was associated with higher RS (> 25: aOR 16.15, 95% CI 15.23–17.13). Cox MVA showed that PR-negative status was associated with worse OS (adjusted hazards ratio [aHR] 1.20, 95% CI 1.10–1.31). There was an interaction with nodal staging and chemotherapy (p = 0.049). Subgroup analyses using Cox MVA showed the magnitude of the chemotherapy benefit was greater among those with pN1a, PR-negative tumors than pN1a, PR-positive tumors (PR-positive: aHR 0.57, 95% CI 0.47–0.67; PR-negative: aHR 0.31, 95% CI 0.20–0.47). It was comparable among those with pN0 tumors regardless of PR status (PR-positive: aHR 0.74, 95% CI 0.66–0.82; PR-negative: aHR 0.63, 95% CI 0.51–0.77). CONCLUSION: PR-negative tumors were independently correlated with higher RS and were associated with greater OS benefits from chemotherapy for pN1a tumors, but not pN0 tumors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-10796-4. BioMed Central 2023-04-11 /pmc/articles/PMC10088125/ /pubmed/37041481 http://dx.doi.org/10.1186/s12885-023-10796-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ma, Sung Jun
Gill, Jasmin
Yendamuri, Keerti
Chatterjee, Udit
Waldman, Olivia
Dunne-Jaffe, Cynthia
Fekrmandi, Fatemeh
Shekher, Rohil
Iovoli, Austin
Yao, Song
Oladeru, Oluwadamilola T.
Singh, Anurag K.
Association of progesterone receptor status with 21-gene recurrence score and survival among patients with estrogen receptor-positive breast cancer
title Association of progesterone receptor status with 21-gene recurrence score and survival among patients with estrogen receptor-positive breast cancer
title_full Association of progesterone receptor status with 21-gene recurrence score and survival among patients with estrogen receptor-positive breast cancer
title_fullStr Association of progesterone receptor status with 21-gene recurrence score and survival among patients with estrogen receptor-positive breast cancer
title_full_unstemmed Association of progesterone receptor status with 21-gene recurrence score and survival among patients with estrogen receptor-positive breast cancer
title_short Association of progesterone receptor status with 21-gene recurrence score and survival among patients with estrogen receptor-positive breast cancer
title_sort association of progesterone receptor status with 21-gene recurrence score and survival among patients with estrogen receptor-positive breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10088125/
https://www.ncbi.nlm.nih.gov/pubmed/37041481
http://dx.doi.org/10.1186/s12885-023-10796-4
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