Capecitabine and lapatinib uptake in surgically resected brain metastases from metastatic breast cancer patients: A prospective study Journal Article


Authors: Morikawa, A.; Peereboom, D. M.; Thorsheim, H. R.; Samala, R.; Balyan, R.; Murphy, C. G.; Lockman, P. R.; Simmons, A.; Weil, R. J.; Tabar, V.; Steeg, P. S.; Smith, Q. R.; Seidman, A. D.
Article Title: Capecitabine and lapatinib uptake in surgically resected brain metastases from metastatic breast cancer patients: A prospective study
Abstract: Background. Breast cancer brain metastases (BCBM) are challenging complications that respond poorly to systemic therapy. The role of the blood-tumor barrier in limiting BCBM drug delivery and efficacy has been debated. Herein, we determined tissue and serum levels of capecitabine, its prodrug metabolites, and lapatinib in women with BCBM resected via medically indicated craniotomy. Methods. Study patients with BCBM requiring surgical resection received either single-dose capecitabine (1250 mg/m(2)) 2-3 h before surgery or 2-5 doses of lapatinib (1250 mg) daily, the last dose 2-3 h before surgery. Serum samples were collected serially on the day of surgery. Drug concentrations were determined in serum and BCBM using liquid chromatography tandem mass spectrometry. Results. Twelve patients were enrolled: 8 for capecitabine and 4 for lapatinib. Measurable drug levels of capecitabine and metabolites, 5'-deoxy-5-fluorocytidine, 5'-deoxy-5-fluorouridine, and 5-fluorouracil, were detected in all BCBM. The ratio of BCBM to serum was higher for 5-fluorouracil than for capecitabine. As for lapatinib, the median BCBM concentrations ranged from 1.0 to 6.5 mM. A high variability (0.19-9.8) was noted for lapatinib BCBM-to-serum ratio. Conclusions. This is the first study to demonstrate that capecitabine and lapatinib penetrate to a significant though variable degree in human BCBM. Drug delivery to BCBM is variable and in many cases appears partially limiting. Elucidating mechanisms that limit drug concentration and innovative approaches to overcome limited drug uptake will be important to improve clinical efficacy of these agents in the central nervous system. Trial registration ID: NCT00795678.
Keywords: capecitabine; breast cancer; tyrosine kinase inhibitor; in-vitro; lapatinib; tissue; p-glycoprotein; brain metastases; lung-cancer; phase-ii; barrier; growth; cns metastases; abcb1; blood-tumor barrier; resistance protein abcg2
Journal Title: Neuro-Oncology
Volume: 17
Issue: 2
ISSN: 1522-8517
Publisher: Oxford University Press  
Date Published: 2015-02-01
Start Page: 289
End Page: 295
Language: English
ACCESSION: WOS:000350138500013
DOI: 10.1093/neuonc/nou141
PROVIDER: wos
PMCID: PMC4288517
PUBMED: 25015089
Notes: Article -- Source: Wos
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  1. Andrew D Seidman
    318 Seidman
  2. Viviane S Tabar
    223 Tabar
  3. Conleth Gerrard Murphy
    18 Murphy