Association of intratumoral pharmacokinetics of fluorouracil with clinical response
- PMID: 7909867
- DOI: 10.1016/s0140-6736(94)92399-x
Association of intratumoral pharmacokinetics of fluorouracil with clinical response
Abstract
In-vivo fluorine-19 nuclear magnetic resonance spectroscopy (NMRS) allows non-invasive, real-time, chemical identification of specific fluorinated compounds inside human tumours after administration of fluorouracil (5-fluorouracil). Kinetic measures of the administered drug and metabolites allow estimation of the tumoral half-life of fluorouracil. We studied 57 patients by 19F NMRS immediately after they had received 600 mg/m2 fluorouracil intravenously. Serial spectra were acquired with the surface coil positioned on the skin above the tumour. We defined an intratumoral half-life of fluorouracil of 20 min or more as indicating trapping of the drug, based on the blood half-life of 8-12 min. 19 patients had intratumoral half-lives indicating trapping of fluorouracil, 27 had half-lives less than 20 min, and 11 had no detectable fluorouracil in their tumours. 8 of 9 evaluable patients whose tumours showed trapping had partial responses to chemotherapy that included fluorouracil compared with only 2 of 25 patients whose tumours did not trap the drug (p = 0.000021). 19F NMRS can identify patients likely to respond to chemotherapy with fluorouracil and could be used clinically to tailor optimum treatment.
Comment in
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Tumour pharmacokinetics?--we do need to know.Lancet. 1994 May 14;343(8907):1174-5. doi: 10.1016/s0140-6736(94)92395-7. Lancet. 1994. PMID: 7909863 No abstract available.
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