Journal
CANCER CHEMOTHERAPY AND PHARMACOLOGY
Volume 64, Issue 3, Pages 509-516Publisher
SPRINGER
DOI: 10.1007/s00280-008-0898-0
Keywords
Microdialysis; Clinical oncology; Pharmacokinetics; Target site; Carboplatin
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Funding
- Cornelis Vrolijk Stichting (IJmuiden, The Netherlands)
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To better understand the mechanisms underlying (in)sensitivity of tumors to anticancer drugs, assessing intra-tumor drug pharmacokinetics (PKs) could be important. We explored the feasibility of microdialysis in tumor tissue for multiple days in a clinical setting, using carboplatin as model drug. Plasma and microdialysate samples from tumor and adipose normal tissues were collected up to 47 h after dosing in eight carboplatin-treated patients with an accessible (sub)cutaneous tumor. Pharmacokinetics were evaluable in tumor tissue in 6/8 patients and in adipose normal tissue in 3/8 patients. Concentration-time curves of unbound platinum in both the tissues followed the pattern of the curves in plasma, with exposure ratios of tissue versus plasma ranging from 0.64 to 1.46. Microdialysis can be successfully employed in ambulant patients for multiple days, which enables one to study tissue PK of anticancer drugs in normal and malignant tissues in more detail.
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