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Carmustine and methotrexate in combination after whole brain radiation therapy in breast cancer patients presenting with brain metastases: a retrospective study

BACKGROUND: Since 1999, patients presenting with brain metastases (BM) from breast cancer (BC) are treated in our institution with a carmustine (BCNU) - methotrexate (MTX) combination. We report here our clinical experience regarding this combination. PATIENTS AND METHODS: Patients were treated by a...

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Autores principales: Jacot, William, Gerlotto-Borne, Marie-Cécile, Thezenas, Simon, Pouderoux, Stéphane, Poujol, Sylvain, About, Mahdi, Romieu, Gilles
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887781/
https://www.ncbi.nlm.nih.gov/pubmed/20525352
http://dx.doi.org/10.1186/1471-2407-10-257
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author Jacot, William
Gerlotto-Borne, Marie-Cécile
Thezenas, Simon
Pouderoux, Stéphane
Poujol, Sylvain
About, Mahdi
Romieu, Gilles
author_facet Jacot, William
Gerlotto-Borne, Marie-Cécile
Thezenas, Simon
Pouderoux, Stéphane
Poujol, Sylvain
About, Mahdi
Romieu, Gilles
author_sort Jacot, William
collection PubMed
description BACKGROUND: Since 1999, patients presenting with brain metastases (BM) from breast cancer (BC) are treated in our institution with a carmustine (BCNU) - methotrexate (MTX) combination. We report here our clinical experience regarding this combination. PATIENTS AND METHODS: Patients were treated by a combination of BCNU 100 mg/m² on day 1 and MTX 600 mg/m² on day 1 and 15 of a 28 day cycle. Treatment was continued until progression or unacceptable toxicity. RESULTS: 50 patients were treated between 1999 and 2007. 94% of the patients presented with concomitant extra-cerebral disease. Median number of previous metastatic setting chemotherapy regimens was 2 (0-5). Median number of cycles was 3 (1-20). There were 11 objective responses (23% [95%CI 12-37]) among 48 evaluable patients. Median progression-free survival and overall survival (OS) were 4.2 (95%CI: 2.8-5.3) and 6.9 (4.2-10.7) months respectively, with a one-year OS rate of 32% (20-46). Median Relative Dose Intensity for BCNU and MTX were 0.98 (0.31-1.1) and 0.96 (0.57-1.66) respectively. There were 2 presumed treatment-related deaths. One patient developed febrile neutropenia. Performance status, BS-BM score and presence of liver metastases were associated with OS in univariate analysis. CONCLUSIONS: This combination appears to be effective and well tolerated in good performance status BC patients presenting with BM.
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spelling pubmed-28877812010-06-19 Carmustine and methotrexate in combination after whole brain radiation therapy in breast cancer patients presenting with brain metastases: a retrospective study Jacot, William Gerlotto-Borne, Marie-Cécile Thezenas, Simon Pouderoux, Stéphane Poujol, Sylvain About, Mahdi Romieu, Gilles BMC Cancer Research Article BACKGROUND: Since 1999, patients presenting with brain metastases (BM) from breast cancer (BC) are treated in our institution with a carmustine (BCNU) - methotrexate (MTX) combination. We report here our clinical experience regarding this combination. PATIENTS AND METHODS: Patients were treated by a combination of BCNU 100 mg/m² on day 1 and MTX 600 mg/m² on day 1 and 15 of a 28 day cycle. Treatment was continued until progression or unacceptable toxicity. RESULTS: 50 patients were treated between 1999 and 2007. 94% of the patients presented with concomitant extra-cerebral disease. Median number of previous metastatic setting chemotherapy regimens was 2 (0-5). Median number of cycles was 3 (1-20). There were 11 objective responses (23% [95%CI 12-37]) among 48 evaluable patients. Median progression-free survival and overall survival (OS) were 4.2 (95%CI: 2.8-5.3) and 6.9 (4.2-10.7) months respectively, with a one-year OS rate of 32% (20-46). Median Relative Dose Intensity for BCNU and MTX were 0.98 (0.31-1.1) and 0.96 (0.57-1.66) respectively. There were 2 presumed treatment-related deaths. One patient developed febrile neutropenia. Performance status, BS-BM score and presence of liver metastases were associated with OS in univariate analysis. CONCLUSIONS: This combination appears to be effective and well tolerated in good performance status BC patients presenting with BM. BioMed Central 2010-06-04 /pmc/articles/PMC2887781/ /pubmed/20525352 http://dx.doi.org/10.1186/1471-2407-10-257 Text en Copyright ©2010 Jacot 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
Jacot, William
Gerlotto-Borne, Marie-Cécile
Thezenas, Simon
Pouderoux, Stéphane
Poujol, Sylvain
About, Mahdi
Romieu, Gilles
Carmustine and methotrexate in combination after whole brain radiation therapy in breast cancer patients presenting with brain metastases: a retrospective study
title Carmustine and methotrexate in combination after whole brain radiation therapy in breast cancer patients presenting with brain metastases: a retrospective study
title_full Carmustine and methotrexate in combination after whole brain radiation therapy in breast cancer patients presenting with brain metastases: a retrospective study
title_fullStr Carmustine and methotrexate in combination after whole brain radiation therapy in breast cancer patients presenting with brain metastases: a retrospective study
title_full_unstemmed Carmustine and methotrexate in combination after whole brain radiation therapy in breast cancer patients presenting with brain metastases: a retrospective study
title_short Carmustine and methotrexate in combination after whole brain radiation therapy in breast cancer patients presenting with brain metastases: a retrospective study
title_sort carmustine and methotrexate in combination after whole brain radiation therapy in breast cancer patients presenting with brain metastases: a retrospective study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887781/
https://www.ncbi.nlm.nih.gov/pubmed/20525352
http://dx.doi.org/10.1186/1471-2407-10-257
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