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The use of fulvestrant before chemotherapy improves survival in hormone-positive breast cancer: a real-life study
BACKGROUND/AIM: We aimed to evaluate the efficacy of fulvestrant and its affecting clinical factors, including the optimal sequencing of fulvestrant and chemotherapy in a real-life cohort. METHODS: The data of 256 metastatic hormone-positive breast cancer patients treated with fulvestrant were evalu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific and Technological Research Council of Turkey (TUBITAK)
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395701/ https://www.ncbi.nlm.nih.gov/pubmed/36422490 http://dx.doi.org/10.55730/1300-0144.5495 |
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author | GÜVEN, Deniz Can YILDIRIM, Hasan Çağrı ERUL, Enes ŞAHİN, Taha Koray ÇAKIR, İbrahim Yahya AKTEPE, Oktay Halit KERTMEN, Neyran DİZDAR, Ömer AKSOY, Sercan |
author_facet | GÜVEN, Deniz Can YILDIRIM, Hasan Çağrı ERUL, Enes ŞAHİN, Taha Koray ÇAKIR, İbrahim Yahya AKTEPE, Oktay Halit KERTMEN, Neyran DİZDAR, Ömer AKSOY, Sercan |
author_sort | GÜVEN, Deniz Can |
collection | PubMed |
description | BACKGROUND/AIM: We aimed to evaluate the efficacy of fulvestrant and its affecting clinical factors, including the optimal sequencing of fulvestrant and chemotherapy in a real-life cohort. METHODS: The data of 256 metastatic hormone-positive breast cancer patients treated with fulvestrant were evaluated. The association of clinical factors with survival was analyzed with Kaplan-Meier and Cox-regression analyses. RESULTS: The median age of patients was 57 years. More than half of the patients used fulvestrant in later lines and after chemotherapy (75.8%). The median progression-free (PFS) and overall survival (OS) of all cohort were 6.05 ± 0.56 and 29.70 ± 1.61 months, respectively. Primary endocrine resistance (HR: 1.989, 95% CI: 1.430–2.766, <0.001), use of fulvestrant after chemotherapy (HR: 1.849, 95% CI: 1.182–2.891, p = 0.007) and visceral metastases (HR: 1.587, 95% CI: 1.128–2.233, p = 0.008) were associated with decreased OS in multivariate analyses. Sixteen patients were treated with trastuzumab and fulvestrant combination. The overall response rate (p = 0.340), disease control rate (p = 0.076), and OS (p = 0.289) and PFS (p = 0.276) were similar to overall cohort. CONCLUSION: In our experience, fulvestrant treatment was associated with comparable OS to clinical trials in a large cohort of patients. Patients treated with fulvestrant before chemotherapy were garnered significantly more benefit. |
format | Online Article Text |
id | pubmed-10395701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Scientific and Technological Research Council of Turkey (TUBITAK) |
record_format | MEDLINE/PubMed |
spelling | pubmed-103957012023-08-03 The use of fulvestrant before chemotherapy improves survival in hormone-positive breast cancer: a real-life study GÜVEN, Deniz Can YILDIRIM, Hasan Çağrı ERUL, Enes ŞAHİN, Taha Koray ÇAKIR, İbrahim Yahya AKTEPE, Oktay Halit KERTMEN, Neyran DİZDAR, Ömer AKSOY, Sercan Turk J Med Sci Research Article BACKGROUND/AIM: We aimed to evaluate the efficacy of fulvestrant and its affecting clinical factors, including the optimal sequencing of fulvestrant and chemotherapy in a real-life cohort. METHODS: The data of 256 metastatic hormone-positive breast cancer patients treated with fulvestrant were evaluated. The association of clinical factors with survival was analyzed with Kaplan-Meier and Cox-regression analyses. RESULTS: The median age of patients was 57 years. More than half of the patients used fulvestrant in later lines and after chemotherapy (75.8%). The median progression-free (PFS) and overall survival (OS) of all cohort were 6.05 ± 0.56 and 29.70 ± 1.61 months, respectively. Primary endocrine resistance (HR: 1.989, 95% CI: 1.430–2.766, <0.001), use of fulvestrant after chemotherapy (HR: 1.849, 95% CI: 1.182–2.891, p = 0.007) and visceral metastases (HR: 1.587, 95% CI: 1.128–2.233, p = 0.008) were associated with decreased OS in multivariate analyses. Sixteen patients were treated with trastuzumab and fulvestrant combination. The overall response rate (p = 0.340), disease control rate (p = 0.076), and OS (p = 0.289) and PFS (p = 0.276) were similar to overall cohort. CONCLUSION: In our experience, fulvestrant treatment was associated with comparable OS to clinical trials in a large cohort of patients. Patients treated with fulvestrant before chemotherapy were garnered significantly more benefit. Scientific and Technological Research Council of Turkey (TUBITAK) 2021-08-26 /pmc/articles/PMC10395701/ /pubmed/36422490 http://dx.doi.org/10.55730/1300-0144.5495 Text en © TÜBİTAK https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License. |
spellingShingle | Research Article GÜVEN, Deniz Can YILDIRIM, Hasan Çağrı ERUL, Enes ŞAHİN, Taha Koray ÇAKIR, İbrahim Yahya AKTEPE, Oktay Halit KERTMEN, Neyran DİZDAR, Ömer AKSOY, Sercan The use of fulvestrant before chemotherapy improves survival in hormone-positive breast cancer: a real-life study |
title | The use of fulvestrant before chemotherapy improves survival in hormone-positive breast cancer: a real-life study |
title_full | The use of fulvestrant before chemotherapy improves survival in hormone-positive breast cancer: a real-life study |
title_fullStr | The use of fulvestrant before chemotherapy improves survival in hormone-positive breast cancer: a real-life study |
title_full_unstemmed | The use of fulvestrant before chemotherapy improves survival in hormone-positive breast cancer: a real-life study |
title_short | The use of fulvestrant before chemotherapy improves survival in hormone-positive breast cancer: a real-life study |
title_sort | use of fulvestrant before chemotherapy improves survival in hormone-positive breast cancer: a real-life study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395701/ https://www.ncbi.nlm.nih.gov/pubmed/36422490 http://dx.doi.org/10.55730/1300-0144.5495 |
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