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Selection of neoadjuvant treatment based on the 21-GENE test results in luminal breast cancer

Neoadjuvant chemotherapy (NAC) is an optimal option in early breast cancer, but in ER-positive/HER2-negative (luminal) is still controversial, although a survival benefit has recently been observed when a histological response by Symmans’ method type 0 or I is achieved. The 21-gene Oncotype DX Breas...

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Autores principales: Morales Murillo, Serafin, Gasol Cudos, Ariadna, Veas Rodriguez, Joel, Canosa Morales, Carles, Melé Olivé, Jordi, Vilardell Villellas, Felip, Sanchez Guzman, Douglas Rene, Iglesias Martínez, Edelmiro, Salud Salvia, Antonieta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900764/
https://www.ncbi.nlm.nih.gov/pubmed/33601299
http://dx.doi.org/10.1016/j.breast.2021.01.001
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author Morales Murillo, Serafin
Gasol Cudos, Ariadna
Veas Rodriguez, Joel
Canosa Morales, Carles
Melé Olivé, Jordi
Vilardell Villellas, Felip
Sanchez Guzman, Douglas Rene
Iglesias Martínez, Edelmiro
Salud Salvia, Antonieta
author_facet Morales Murillo, Serafin
Gasol Cudos, Ariadna
Veas Rodriguez, Joel
Canosa Morales, Carles
Melé Olivé, Jordi
Vilardell Villellas, Felip
Sanchez Guzman, Douglas Rene
Iglesias Martínez, Edelmiro
Salud Salvia, Antonieta
author_sort Morales Murillo, Serafin
collection PubMed
description Neoadjuvant chemotherapy (NAC) is an optimal option in early breast cancer, but in ER-positive/HER2-negative (luminal) is still controversial, although a survival benefit has recently been observed when a histological response by Symmans’ method type 0 or I is achieved. The 21-gene Oncotype DX Breast Recurrence Score® assay (Oncotype DX®) is a validated test to assess the survival benefit of adjuvant chemotherapy in these patients but its role in the neoadjuvant setting is less established. We analyzed the results of the Oncotype DX® test in a cohort of 122 consecutive patients selected to receive NAC based on classical clinicopathological parameters and the correlation between the Oncotype DX® results and the pathological response assessed by Symmans’ method. Median age was 56.5 (range 31–84) years. Initial tumor size was T1 (<20 mm) in 46 patients (37.7%), 57 (46.7%) had a T2 tumor (20–50 mm), and 19 (15.6%) had a tumor size more than 50 mm. 59 (48.4%) had axillary node involvement. The median expression estrogen and progesteron receptors by immunohistochemistry was 280 and 120 respectively and median Ki67 index was 28%. The Recurrence Score (RS) results were <11 in 21 patients (17.2%) patients, RS 11 to 25 in 58 (47.5%), and RS > 25 in 43 (35.2%). Considering the Oncotype DX test results, neoadjuvant chemotherapy was administered to 60 patients (49%), 11 (9%) received adjuvant chemotherapy and 51 (42%) no chemotherapy. Testing with the assay has therefore led to 42% fewer chemotherapy treatments. Among 60 patients receiving NAC, pathologic response was achieved for 5 patients (8.3%) with RCB-0 and 15 RCB-1 (25%). We did not find any pathological response RCB-0 and RCB-I in the 20 patients who received NAC and had a Recurrence Score result <21 for the premenopausal group, or a RS result <25 for the postmenopausal group. For patients with highest Recurrence Score results (RS > 21 or 25 according to menopausal status) it was 12% (5/40) RCB-0 and 40% (16/40) RCB-I. CONCLUSIONS: The Oncotype DX test could be a useful tool to select patients candidates for neoadjuvant chemotherapy in luminal breast cancer. Neoadjuvant chemotherapy could be avoided in 42% of patients. We found a correlation between Recurrence Score results and pathological response with 14% of RCB-0 and a total of 47% of significant pathological response type RCB-0 and RCB-I in patients with highest Recurrence Score results. Interestingly, patients with a Recurrence Score result inferior to 32 did not get any histological response type 0 and only 5% RCB-I.
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spelling pubmed-79007642021-03-03 Selection of neoadjuvant treatment based on the 21-GENE test results in luminal breast cancer Morales Murillo, Serafin Gasol Cudos, Ariadna Veas Rodriguez, Joel Canosa Morales, Carles Melé Olivé, Jordi Vilardell Villellas, Felip Sanchez Guzman, Douglas Rene Iglesias Martínez, Edelmiro Salud Salvia, Antonieta Breast Original Article Neoadjuvant chemotherapy (NAC) is an optimal option in early breast cancer, but in ER-positive/HER2-negative (luminal) is still controversial, although a survival benefit has recently been observed when a histological response by Symmans’ method type 0 or I is achieved. The 21-gene Oncotype DX Breast Recurrence Score® assay (Oncotype DX®) is a validated test to assess the survival benefit of adjuvant chemotherapy in these patients but its role in the neoadjuvant setting is less established. We analyzed the results of the Oncotype DX® test in a cohort of 122 consecutive patients selected to receive NAC based on classical clinicopathological parameters and the correlation between the Oncotype DX® results and the pathological response assessed by Symmans’ method. Median age was 56.5 (range 31–84) years. Initial tumor size was T1 (<20 mm) in 46 patients (37.7%), 57 (46.7%) had a T2 tumor (20–50 mm), and 19 (15.6%) had a tumor size more than 50 mm. 59 (48.4%) had axillary node involvement. The median expression estrogen and progesteron receptors by immunohistochemistry was 280 and 120 respectively and median Ki67 index was 28%. The Recurrence Score (RS) results were <11 in 21 patients (17.2%) patients, RS 11 to 25 in 58 (47.5%), and RS > 25 in 43 (35.2%). Considering the Oncotype DX test results, neoadjuvant chemotherapy was administered to 60 patients (49%), 11 (9%) received adjuvant chemotherapy and 51 (42%) no chemotherapy. Testing with the assay has therefore led to 42% fewer chemotherapy treatments. Among 60 patients receiving NAC, pathologic response was achieved for 5 patients (8.3%) with RCB-0 and 15 RCB-1 (25%). We did not find any pathological response RCB-0 and RCB-I in the 20 patients who received NAC and had a Recurrence Score result <21 for the premenopausal group, or a RS result <25 for the postmenopausal group. For patients with highest Recurrence Score results (RS > 21 or 25 according to menopausal status) it was 12% (5/40) RCB-0 and 40% (16/40) RCB-I. CONCLUSIONS: The Oncotype DX test could be a useful tool to select patients candidates for neoadjuvant chemotherapy in luminal breast cancer. Neoadjuvant chemotherapy could be avoided in 42% of patients. We found a correlation between Recurrence Score results and pathological response with 14% of RCB-0 and a total of 47% of significant pathological response type RCB-0 and RCB-I in patients with highest Recurrence Score results. Interestingly, patients with a Recurrence Score result inferior to 32 did not get any histological response type 0 and only 5% RCB-I. Elsevier 2021-01-15 /pmc/articles/PMC7900764/ /pubmed/33601299 http://dx.doi.org/10.1016/j.breast.2021.01.001 Text en © 2021 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Morales Murillo, Serafin
Gasol Cudos, Ariadna
Veas Rodriguez, Joel
Canosa Morales, Carles
Melé Olivé, Jordi
Vilardell Villellas, Felip
Sanchez Guzman, Douglas Rene
Iglesias Martínez, Edelmiro
Salud Salvia, Antonieta
Selection of neoadjuvant treatment based on the 21-GENE test results in luminal breast cancer
title Selection of neoadjuvant treatment based on the 21-GENE test results in luminal breast cancer
title_full Selection of neoadjuvant treatment based on the 21-GENE test results in luminal breast cancer
title_fullStr Selection of neoadjuvant treatment based on the 21-GENE test results in luminal breast cancer
title_full_unstemmed Selection of neoadjuvant treatment based on the 21-GENE test results in luminal breast cancer
title_short Selection of neoadjuvant treatment based on the 21-GENE test results in luminal breast cancer
title_sort selection of neoadjuvant treatment based on the 21-gene test results in luminal breast cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900764/
https://www.ncbi.nlm.nih.gov/pubmed/33601299
http://dx.doi.org/10.1016/j.breast.2021.01.001
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