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Nasal septum perforation: a side effect of bevacizumab chemotherapy in breast cancer patients
BACKGROUND: Bevacizumab is an anti-vascular endothelial growth factor approved in association with paclitaxel or docetaxel as first line in patients (pts) with metastatic breast cancer. Rare cases of nasal septum perforations have been reported. We report our experience of nasal perforation in breas...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2966623/ https://www.ncbi.nlm.nih.gov/pubmed/20736943 http://dx.doi.org/10.1038/sj.bjc.6605828 |
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author | Mailliez, A Baldini, C Van, J T Servent, V Mallet, Y Bonneterre, J |
author_facet | Mailliez, A Baldini, C Van, J T Servent, V Mallet, Y Bonneterre, J |
author_sort | Mailliez, A |
collection | PubMed |
description | BACKGROUND: Bevacizumab is an anti-vascular endothelial growth factor approved in association with paclitaxel or docetaxel as first line in patients (pts) with metastatic breast cancer. Rare cases of nasal septum perforations have been reported. We report our experience of nasal perforation in breast cancer pts receiving bevacizumab and chemotherapy either in the adjuvant or in the metastatic settings. METHODS: Between 1 January and 31 December 2009, 70 pts received bevacizumab together with chemotherapy. All the pts who had received bevacizumab were referred to the ENT specialist. Symptoms potentially related were looked for. Side effects were graded according to CTCAE. RESULTS: Five nasal septum perforations were diagnosed (5 out of 70; 7.14%). Bevacizumab dose was 15 mg kg(−1) 3 weekly. Three pts were metastatic. Bevacizumab was associated with docetaxel (100 mg m(−2) every 3 weeks) in two pts and with weekly paclitaxel in one. The last two pts received bevacizumab in combination with anthracyclin and then taxanes in the adjuvant setting. In these two cases, nasal septum perforation occurred at the time of docetaxel treatment. CONCLUSION: A high incidence of nasal septum perforation has been shown in pts with breast cancer receiving bevacizumab together with chemotherapy. Several mechanisms could be involved (mucositis, delayed tissue repair, antiangiogenic action of taxanes). |
format | Text |
id | pubmed-2966623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-29666232011-09-07 Nasal septum perforation: a side effect of bevacizumab chemotherapy in breast cancer patients Mailliez, A Baldini, C Van, J T Servent, V Mallet, Y Bonneterre, J Br J Cancer Clinical Study BACKGROUND: Bevacizumab is an anti-vascular endothelial growth factor approved in association with paclitaxel or docetaxel as first line in patients (pts) with metastatic breast cancer. Rare cases of nasal septum perforations have been reported. We report our experience of nasal perforation in breast cancer pts receiving bevacizumab and chemotherapy either in the adjuvant or in the metastatic settings. METHODS: Between 1 January and 31 December 2009, 70 pts received bevacizumab together with chemotherapy. All the pts who had received bevacizumab were referred to the ENT specialist. Symptoms potentially related were looked for. Side effects were graded according to CTCAE. RESULTS: Five nasal septum perforations were diagnosed (5 out of 70; 7.14%). Bevacizumab dose was 15 mg kg(−1) 3 weekly. Three pts were metastatic. Bevacizumab was associated with docetaxel (100 mg m(−2) every 3 weeks) in two pts and with weekly paclitaxel in one. The last two pts received bevacizumab in combination with anthracyclin and then taxanes in the adjuvant setting. In these two cases, nasal septum perforation occurred at the time of docetaxel treatment. CONCLUSION: A high incidence of nasal septum perforation has been shown in pts with breast cancer receiving bevacizumab together with chemotherapy. Several mechanisms could be involved (mucositis, delayed tissue repair, antiangiogenic action of taxanes). Nature Publishing Group 2010-09-07 2010-08-24 /pmc/articles/PMC2966623/ /pubmed/20736943 http://dx.doi.org/10.1038/sj.bjc.6605828 Text en Copyright © 2010 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This 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 license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license 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 license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Study Mailliez, A Baldini, C Van, J T Servent, V Mallet, Y Bonneterre, J Nasal septum perforation: a side effect of bevacizumab chemotherapy in breast cancer patients |
title | Nasal septum perforation: a side effect of bevacizumab chemotherapy in breast cancer patients |
title_full | Nasal septum perforation: a side effect of bevacizumab chemotherapy in breast cancer patients |
title_fullStr | Nasal septum perforation: a side effect of bevacizumab chemotherapy in breast cancer patients |
title_full_unstemmed | Nasal septum perforation: a side effect of bevacizumab chemotherapy in breast cancer patients |
title_short | Nasal septum perforation: a side effect of bevacizumab chemotherapy in breast cancer patients |
title_sort | nasal septum perforation: a side effect of bevacizumab chemotherapy in breast cancer patients |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2966623/ https://www.ncbi.nlm.nih.gov/pubmed/20736943 http://dx.doi.org/10.1038/sj.bjc.6605828 |
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