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Salvage therapy of pretreated advanced breast cancer with bevacizumab and paclitaxel every two weeks: a retrospective case review study
BACKGROUND: Targeting angiogenesis is nowadays one of the most promising approaches for breast cancer. Bevacizumab (BEV), a VEGF-trap monoclonal antibody, was recently approved in combination with paclitaxel (PAC) for the first line treatment of advanced breast cancer (ABC). The activity of this com...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2759965/ https://www.ncbi.nlm.nih.gov/pubmed/19775466 http://dx.doi.org/10.1186/1471-2407-9-338 |
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author | Ardavanis, Alexandros Doufexis, Dimitrios Kountourakis, Panteleimon Malliou, Savvoula Karagiannis, Athanasios Kardara, Evgenia Sykoutri, Despina Charalampia, Margari Rigatos, Gerasimos |
author_facet | Ardavanis, Alexandros Doufexis, Dimitrios Kountourakis, Panteleimon Malliou, Savvoula Karagiannis, Athanasios Kardara, Evgenia Sykoutri, Despina Charalampia, Margari Rigatos, Gerasimos |
author_sort | Ardavanis, Alexandros |
collection | PubMed |
description | BACKGROUND: Targeting angiogenesis is nowadays one of the most promising approaches for breast cancer. Bevacizumab (BEV), a VEGF-trap monoclonal antibody, was recently approved in combination with paclitaxel (PAC) for the first line treatment of advanced breast cancer (ABC). The activity of this combination in pretreated patients is not known. METHODS: Patients with pretreated ABC and progressive disease received BEV 10 mg/kg with PAC 135 mg/m(2 )every two weeks for six months and then maintenance with BEV 15 mg/kg every three weeks until progression. This regimen was chosen for better patient convenience, while maintaining the same dose intensity for both drugs. RESULTS: 42 patients were reviewed retrospectively (41 f, 1 m, mean age 57 years). Overall response rate was 35.7%. Stable disease was observed in 45.2% of patients, whereas 14.3% of patients progressed. The median overall survival was greater than 20 months, with a one year rate of 83.4%. The median progression free survival was 12.1 months, with a one year rate of 51.8%. Toxicity was in general acceptable. CONCLUSION: This biweekly BEV/PAC combination seems to be active with acceptable toxicity in pretreated ABC with an advantage over the weekly regimen regarding quality of life and preservation of resources. |
format | Text |
id | pubmed-2759965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27599652009-10-11 Salvage therapy of pretreated advanced breast cancer with bevacizumab and paclitaxel every two weeks: a retrospective case review study Ardavanis, Alexandros Doufexis, Dimitrios Kountourakis, Panteleimon Malliou, Savvoula Karagiannis, Athanasios Kardara, Evgenia Sykoutri, Despina Charalampia, Margari Rigatos, Gerasimos BMC Cancer Research Article BACKGROUND: Targeting angiogenesis is nowadays one of the most promising approaches for breast cancer. Bevacizumab (BEV), a VEGF-trap monoclonal antibody, was recently approved in combination with paclitaxel (PAC) for the first line treatment of advanced breast cancer (ABC). The activity of this combination in pretreated patients is not known. METHODS: Patients with pretreated ABC and progressive disease received BEV 10 mg/kg with PAC 135 mg/m(2 )every two weeks for six months and then maintenance with BEV 15 mg/kg every three weeks until progression. This regimen was chosen for better patient convenience, while maintaining the same dose intensity for both drugs. RESULTS: 42 patients were reviewed retrospectively (41 f, 1 m, mean age 57 years). Overall response rate was 35.7%. Stable disease was observed in 45.2% of patients, whereas 14.3% of patients progressed. The median overall survival was greater than 20 months, with a one year rate of 83.4%. The median progression free survival was 12.1 months, with a one year rate of 51.8%. Toxicity was in general acceptable. CONCLUSION: This biweekly BEV/PAC combination seems to be active with acceptable toxicity in pretreated ABC with an advantage over the weekly regimen regarding quality of life and preservation of resources. BioMed Central 2009-09-23 /pmc/articles/PMC2759965/ /pubmed/19775466 http://dx.doi.org/10.1186/1471-2407-9-338 Text en Copyright ©2009 Ardavanis et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Ardavanis, Alexandros Doufexis, Dimitrios Kountourakis, Panteleimon Malliou, Savvoula Karagiannis, Athanasios Kardara, Evgenia Sykoutri, Despina Charalampia, Margari Rigatos, Gerasimos Salvage therapy of pretreated advanced breast cancer with bevacizumab and paclitaxel every two weeks: a retrospective case review study |
title | Salvage therapy of pretreated advanced breast cancer with bevacizumab and paclitaxel every two weeks: a retrospective case review study |
title_full | Salvage therapy of pretreated advanced breast cancer with bevacizumab and paclitaxel every two weeks: a retrospective case review study |
title_fullStr | Salvage therapy of pretreated advanced breast cancer with bevacizumab and paclitaxel every two weeks: a retrospective case review study |
title_full_unstemmed | Salvage therapy of pretreated advanced breast cancer with bevacizumab and paclitaxel every two weeks: a retrospective case review study |
title_short | Salvage therapy of pretreated advanced breast cancer with bevacizumab and paclitaxel every two weeks: a retrospective case review study |
title_sort | salvage therapy of pretreated advanced breast cancer with bevacizumab and paclitaxel every two weeks: a retrospective case review study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2759965/ https://www.ncbi.nlm.nih.gov/pubmed/19775466 http://dx.doi.org/10.1186/1471-2407-9-338 |
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