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Summary
August 2006, Vol. 7, No. 12, Pages 1633-1639
, DOI 10.1517/14656566.7.12.1633
Capecitabine in carcinoma of the pancreasDavid B Smith1Consultant in Medical Oncology, Clatterbridge Centre for Oncology, Bebington, Wirral, Merseyside, L63 4JY, UK. david.smith@ccotrust.nhs.uk 2Professor of Surgery, Division of Surgery and Oncology, University of Liverpool, Fifth Floor UCD Building, Daulby Street, Liverpool, L69 3GA, UK Capecitabine is an oral prodrug of 5-fluorouracil, which is converted to 5-fluorouracil by three sequential enzymatic reactions. The final requisite enzyme, thymidine phosphorylase, is present at consistently higher levels in tumours compared with normal tissues, thereby suggesting that 5-fluorouracil that is delivered in this way may benefit from an element of tumour targeting and thus enhanced selectivity and better tolerability. Capecitabine has been shown to have single-agent activity in advanced carcinoma of the pancreas and to improve response rates and survival when administered in combination with gemcitabine compared with gemcitabine alone. This paper reviews the pharmacology and clinical data that are relevant to the use of capecitabine in pancreatic cancer. |
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