Irinotecan (CPT-11): Recent Developments and Future Directions–Colorectal Cancer and Beyond
Open Access
- 1 February 2001
- journal article
- review article
- Published by Oxford University Press (OUP) in The Oncologist
- Vol. 6 (1) , 66-80
- https://doi.org/10.1634/theoncologist.6-1-66
Abstract
Since its approval in the United States in 1996, irinotecan (CPT-11, Camptosar®, Pharmacia Corp.; Peapack, NJ) has undergone extensive clinical evaluation. In the past five years, the focus of development has evolved from evaluation of single-agent activity in refractory disease settings to evaluation of front-line irinotecan-based combination chemotherapy regimens and integration of irinotecan into combined modality regimens. Important studies have been performed clarifying the role of irinotecan in treating colorectal and other gastrointestinal cancers, small cell and non-small cell lung cancer, and a variety of other malignancies. Preclinical studies performed in conjunction with these clinical trials have also provided significant insights into the pharmacology, metabolism, mechanisms of resistance, and molecular determinants of response. This review summarizes that progress, focusing on the achievements of the past five years.Keywords
This publication has 46 references indexed in Scilit:
- Phenotype-genotype correlation of in vitro SN-38 (active metabolite of irinotecan) and bilirubin glucuronidation in human liver tissue with UGT1A1 promoter polymorphismClinical Pharmacology & Therapeutics, 1999
- CPT-11 converting carboxylesterase and topoisomerase I activities in tumour and normal colon and liver tissuesBritish Journal of Cancer, 1999
- Combination of irinotecan (CPT11) and 5-fluorouracil with an analysis of cellular determinants of drug activityBiochemical Pharmacology, 1998
- Sequence effect of irinotecan (CPT-11) and topoisomerase II inhibitors in vivoCancer Chemotherapy and Pharmacology, 1998
- Multiplicity of biliary excretion mechanisms for the camptothecin derivative irinotecan (CPT-11), its metabolite SN-38, and its glucuronide: role of canalicular multispecific organic anion transporter and P-glycoprotein.Cancer Chemotherapy and Pharmacology, 1998
- Cellular interactions of 5-fluorouracil and the camptothecin analogue CPT-11 (irinotecan) in a human colorectal carcinoma cell lineBiochemical Pharmacology, 1998
- Sequence‐dependent activity of the irinotecan‐5FU combination in human colon‐cancer model HT‐29 in vitro and in vivoInternational Journal of Cancer, 1997
- Severe CPT-11 toxicity in patients with Gilbert's syndrome: Two case reportsAnnals of Oncology, 1997
- Modulation of glucuronidation of SN-38, the active metabolite of irinotecan, by valproic acid and phenobarbitalCancer Chemotherapy and Pharmacology, 1997
- Effects of CPT‐11 in combination with other anti‐cancer agents in cultureInternational Journal of Cancer, 1992