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Dramatic Regression of Multiple Brain Metastases from Breast Cancer with Capecitabine: Another Arrow at the Bow? 

Authors: A. Fabi a;  A. Vidiri b;  G. Ferretti a;  A. Felici a;  P. Papaldo a;  P. Carlini a;  A. Mirri c;  C. Nuzzo a; F. Cognetti a
Affiliations:   a Department of Medical Oncology, Regina Elena National Cancer Institute, Rome, Italy
b Department of Diagnostic of Imaging, Regina Elena National Cancer Institute, Rome, Italy
c Service of Radiotherapy, Regina Elena National Cancer Institute, Rome, Italy
DOI: 10.1080/07357900600705805
Publication Frequency: 10 issues per year
Published in: journal Cancer Investigation, Volume 24, Issue 4 July 2006 , pages 466 - 468
Subject: Oncology;
Formats available: HTML (English) : PDF (English)
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Abstract

Several chemotherapic agents, which are active againstbreast cancer, penetrate poorly into the central nervous system. Despite its limited brain penetration, 5-fluorouracil has been a component of effective regimens for brain metastases. Capecitabine is a recently developed oral prodrug that is converted into 5-fluorouracil by sequential enzymatic steps. Thymidine phosphorylase (TP) is the final enzyme responsible for Capecitabine activation. Studies have demonstrated that high intratumoral levels of TP and low levels of its catabolite dihydropyrimidine-dehydrogenase are correlated with the capecitabine response. The penetration of Capecitabine across the brain-blood barrier remains unknown; we report the case of and discuss a breast cancer patient who had an interesting response of brain metastases with Capecitabine in monochemotherapy before brain irradiation.
Keywords: brain metastasis; capecitabine breast cancer
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