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Incidence of cerebral metastases in patients treated with trastuzumab for metastatic breast cancer

Trastuzumab is an effective treatment for patients with metastatic breast cancer (MBC) that overexpresses HER-2. A high incidence of brain metastases (BM) has been noted in patients receiving trastuzumab. A retrospective chart review was conducted of 100 patients commencing trastuzumab for metastati...

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Autores principales: Clayton, A J, Danson, S, Jolly, S, Ryder, W D J, Burt, P A, Stewart, A L, Wilkinson, P M, Welch, R S, Magee, B, Wilson, G, Howell, A, Wardley, A M
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364775/
https://www.ncbi.nlm.nih.gov/pubmed/15266327
http://dx.doi.org/10.1038/sj.bjc.6601970
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author Clayton, A J
Danson, S
Jolly, S
Ryder, W D J
Burt, P A
Stewart, A L
Wilkinson, P M
Welch, R S
Magee, B
Wilson, G
Howell, A
Wardley, A M
author_facet Clayton, A J
Danson, S
Jolly, S
Ryder, W D J
Burt, P A
Stewart, A L
Wilkinson, P M
Welch, R S
Magee, B
Wilson, G
Howell, A
Wardley, A M
author_sort Clayton, A J
collection PubMed
description Trastuzumab is an effective treatment for patients with metastatic breast cancer (MBC) that overexpresses HER-2. A high incidence of brain metastases (BM) has been noted in patients receiving trastuzumab. A retrospective chart review was conducted of 100 patients commencing trastuzumab for metastatic breast cancer from July 1999 to December 2002, at the Christie Hospital. Seven patients were excluded; five patients developed central nervous system metastases prior to starting trastuzumab, and inadequate data were available for two. Out of the remaining 93 patients, 23 (25%) have developed BM to date. In all, 46 patients have died, and of these 18 (39%) have been diagnosed with BM prior to death. Of the 23 patients developing BM, 18 (78%) were hormone receptor negative and 18 (78%) had visceral disease. Univariate analysis showed a significant association between the development of cerebral disease and both hormone receptor status and the presence of visceral disease. In conclusion, a high proportion of patients with MBC treated with trastuzumab develop symptomatic cerebral metastases. HER-2-positive breast cancer may have a predilection for the brain, or trastuzumab therapy may change the disease pattern by prolonging survival. New strategies to address this problem require investigation in this group of patients.
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spelling pubmed-23647752009-09-10 Incidence of cerebral metastases in patients treated with trastuzumab for metastatic breast cancer Clayton, A J Danson, S Jolly, S Ryder, W D J Burt, P A Stewart, A L Wilkinson, P M Welch, R S Magee, B Wilson, G Howell, A Wardley, A M Br J Cancer Clinical Trastuzumab is an effective treatment for patients with metastatic breast cancer (MBC) that overexpresses HER-2. A high incidence of brain metastases (BM) has been noted in patients receiving trastuzumab. A retrospective chart review was conducted of 100 patients commencing trastuzumab for metastatic breast cancer from July 1999 to December 2002, at the Christie Hospital. Seven patients were excluded; five patients developed central nervous system metastases prior to starting trastuzumab, and inadequate data were available for two. Out of the remaining 93 patients, 23 (25%) have developed BM to date. In all, 46 patients have died, and of these 18 (39%) have been diagnosed with BM prior to death. Of the 23 patients developing BM, 18 (78%) were hormone receptor negative and 18 (78%) had visceral disease. Univariate analysis showed a significant association between the development of cerebral disease and both hormone receptor status and the presence of visceral disease. In conclusion, a high proportion of patients with MBC treated with trastuzumab develop symptomatic cerebral metastases. HER-2-positive breast cancer may have a predilection for the brain, or trastuzumab therapy may change the disease pattern by prolonging survival. New strategies to address this problem require investigation in this group of patients. Nature Publishing Group 2004-08-16 2004-07-20 /pmc/articles/PMC2364775/ /pubmed/15266327 http://dx.doi.org/10.1038/sj.bjc.6601970 Text en Copyright © 2004 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
Clayton, A J
Danson, S
Jolly, S
Ryder, W D J
Burt, P A
Stewart, A L
Wilkinson, P M
Welch, R S
Magee, B
Wilson, G
Howell, A
Wardley, A M
Incidence of cerebral metastases in patients treated with trastuzumab for metastatic breast cancer
title Incidence of cerebral metastases in patients treated with trastuzumab for metastatic breast cancer
title_full Incidence of cerebral metastases in patients treated with trastuzumab for metastatic breast cancer
title_fullStr Incidence of cerebral metastases in patients treated with trastuzumab for metastatic breast cancer
title_full_unstemmed Incidence of cerebral metastases in patients treated with trastuzumab for metastatic breast cancer
title_short Incidence of cerebral metastases in patients treated with trastuzumab for metastatic breast cancer
title_sort incidence of cerebral metastases in patients treated with trastuzumab for metastatic breast cancer
topic Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364775/
https://www.ncbi.nlm.nih.gov/pubmed/15266327
http://dx.doi.org/10.1038/sj.bjc.6601970
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