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Tailoring neoadjuvant chemotherapy for patients with breast cancer who have achieved pathologic complete response
BACKGROUND: We retrospectively examined whether different cycles of chemotherapy affected the prognosis of patients who achieved a pathologic complete response (pCR). METHODS: We reviewed data from patients who achieved pCR after neoadjuvant chemotherapy (NACT) between 2008 and 2018. In total, 286 p...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798334/ https://www.ncbi.nlm.nih.gov/pubmed/35117465 http://dx.doi.org/10.21037/tcr.2020.01.01 |
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author | Li, Xianjun Liu, Yang Shan, Ming Xu, Bingqi Lu, Yubo Zhang, Guoqiang |
author_facet | Li, Xianjun Liu, Yang Shan, Ming Xu, Bingqi Lu, Yubo Zhang, Guoqiang |
author_sort | Li, Xianjun |
collection | PubMed |
description | BACKGROUND: We retrospectively examined whether different cycles of chemotherapy affected the prognosis of patients who achieved a pathologic complete response (pCR). METHODS: We reviewed data from patients who achieved pCR after neoadjuvant chemotherapy (NACT) between 2008 and 2018. In total, 286 patients were divided into three groups: group one (n=148, 52%) completed standard chemotherapy cycles before surgery, group two (n=81, 28%) did not complete standard chemotherapy cycles before surgery or received chemotherapy after surgery, and group three (n=57, 20%) did not complete standard chemotherapy cycles before surgery but completed them after surgery. Recurrence-free survival (RFS) was estimated using the Kaplan-Meier method, and differences between groups were evaluated by the log-rank test. Cox proportional hazards regression analysis was adjusted for different NACT groups, age, Ki-67 levels, and clinical stages. RESULTS: After a median follow-up of 26 months, there were no significant differences in RFS among the NACT groups (P=0.14). Multivariate analysis showed that Ki-67 ≥40% (P=0.03) and clinical stage (IIIB + IIIC) (P=0.002) might be risk factors for recurrence in patients with pCR. There were no significant differences in survival among subgroups according to Ki-67 levels and clinical stages. CONCLUSIONS: Our study suggests that, even with pCR, patients with baseline stage IIIB or IIIC or Ki-67 levels ≥40% may have an increased risk of recurrence. The RFS of patients with pCR was not associated with the completion of standard chemotherapy cycles, even in high-risk patients. Therefore, the prevention of excessive chemotherapeutic treatment by de-escalation is necessary for patients with pCR. |
format | Online Article Text |
id | pubmed-8798334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87983342022-02-02 Tailoring neoadjuvant chemotherapy for patients with breast cancer who have achieved pathologic complete response Li, Xianjun Liu, Yang Shan, Ming Xu, Bingqi Lu, Yubo Zhang, Guoqiang Transl Cancer Res Original Article BACKGROUND: We retrospectively examined whether different cycles of chemotherapy affected the prognosis of patients who achieved a pathologic complete response (pCR). METHODS: We reviewed data from patients who achieved pCR after neoadjuvant chemotherapy (NACT) between 2008 and 2018. In total, 286 patients were divided into three groups: group one (n=148, 52%) completed standard chemotherapy cycles before surgery, group two (n=81, 28%) did not complete standard chemotherapy cycles before surgery or received chemotherapy after surgery, and group three (n=57, 20%) did not complete standard chemotherapy cycles before surgery but completed them after surgery. Recurrence-free survival (RFS) was estimated using the Kaplan-Meier method, and differences between groups were evaluated by the log-rank test. Cox proportional hazards regression analysis was adjusted for different NACT groups, age, Ki-67 levels, and clinical stages. RESULTS: After a median follow-up of 26 months, there were no significant differences in RFS among the NACT groups (P=0.14). Multivariate analysis showed that Ki-67 ≥40% (P=0.03) and clinical stage (IIIB + IIIC) (P=0.002) might be risk factors for recurrence in patients with pCR. There were no significant differences in survival among subgroups according to Ki-67 levels and clinical stages. CONCLUSIONS: Our study suggests that, even with pCR, patients with baseline stage IIIB or IIIC or Ki-67 levels ≥40% may have an increased risk of recurrence. The RFS of patients with pCR was not associated with the completion of standard chemotherapy cycles, even in high-risk patients. Therefore, the prevention of excessive chemotherapeutic treatment by de-escalation is necessary for patients with pCR. AME Publishing Company 2020-02 /pmc/articles/PMC8798334/ /pubmed/35117465 http://dx.doi.org/10.21037/tcr.2020.01.01 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Original Article Li, Xianjun Liu, Yang Shan, Ming Xu, Bingqi Lu, Yubo Zhang, Guoqiang Tailoring neoadjuvant chemotherapy for patients with breast cancer who have achieved pathologic complete response |
title | Tailoring neoadjuvant chemotherapy for patients with breast cancer who have achieved pathologic complete response |
title_full | Tailoring neoadjuvant chemotherapy for patients with breast cancer who have achieved pathologic complete response |
title_fullStr | Tailoring neoadjuvant chemotherapy for patients with breast cancer who have achieved pathologic complete response |
title_full_unstemmed | Tailoring neoadjuvant chemotherapy for patients with breast cancer who have achieved pathologic complete response |
title_short | Tailoring neoadjuvant chemotherapy for patients with breast cancer who have achieved pathologic complete response |
title_sort | tailoring neoadjuvant chemotherapy for patients with breast cancer who have achieved pathologic complete response |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798334/ https://www.ncbi.nlm.nih.gov/pubmed/35117465 http://dx.doi.org/10.21037/tcr.2020.01.01 |
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