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Increased oral bioavailability of topotecan in combination with the breast cancer resistance protein and P-glycoprotein inhibitor GF120918.
- Source :
-
Journal of clinical oncology : official journal of the American Society of Clinical Oncology [J Clin Oncol] 2002 Jul 01; Vol. 20 (13), pp. 2943-50. - Publication Year :
- 2002
-
Abstract
- Purpose: We discovered that breast cancer resistance protein (BCRP), a recently identified adenosine triphosphate-binding cassette drug transporter, substantially limits the oral bioavailability of topotecan in mdr1a/1b(-/-) P-glycoprotein (P-gp) knockout and wild-type mice. GF120918 is a potent inhibitor of BCRP and P-gp. The aim was to increase the bioavailability of topotecan by GF120918.<br />Patients and Methods: In cohort A, eight patients received 1.0 mg/m(2) oral topotecan with or without coadministration of one single oral dose of 1,000 mg GF120918 (day 1 or day 8). In cohort B, eight other patients received 1.0 mg/m(2) intravenous topotecan with or without 1,000 mg oral GF120918 to study the effect of GF120918 on the systemic clearance of topotecan.<br />Results: After oral topotecan, the mean area under the plasma concentration-time curve (AUC) of total topotecan increased significantly from 32.4 +/- 9.6 microg.h/L without GF120918 to 78.7 +/- 20.6 microg.h/L when GF120918 was coadministered (P =.008). The mean maximum plasma concentration of total topotecan increased from 4.1 +/- 1.5 microg/L without GF120918 to 11.5 +/- 2.4 microg/L with GF120918 (P =.008). The apparent bioavailability in this cohort increased significantly from 40.0% (range, 32% to 47%) to 97.1% (range, 91% to 120%) (P =.008). Interpatient variability of the apparent bioavailability was 17% without and 11% with GF120918. After intravenous administration of topotecan, coadministration of oral GF120918 had a small but statistically significant effect on the AUC and systemic clearance of total topotecan but no statistically significant effect on maximum plasma concentration and terminal half-life of total topotecan.<br />Conclusion: Coadministration of the BCRP and P-gp inhibitor GF120918 resulted in a significant increase of the systemic exposure of oral topotecan. The apparent oral bioavailability increased from 40.0% without to 97.1% with GF120918.
- Subjects :
- ATP Binding Cassette Transporter, Subfamily G, Member 2
Acridines pharmacology
Administration, Oral
Adult
Antineoplastic Agents administration & dosage
Biological Availability
Drug Administration Schedule
Drug Resistance, Multiple
Drug Resistance, Neoplasm
Enzyme Inhibitors administration & dosage
Female
Humans
Isoquinolines pharmacology
Middle Aged
Neoplasm Proteins antagonists & inhibitors
Topotecan administration & dosage
ATP Binding Cassette Transporter, Subfamily B, Member 1 antagonists & inhibitors
ATP-Binding Cassette Transporters antagonists & inhibitors
Acridines therapeutic use
Antineoplastic Agents pharmacokinetics
Breast Neoplasms drug therapy
Breast Neoplasms metabolism
Enzyme Inhibitors pharmacokinetics
Isoquinolines therapeutic use
Tetrahydroisoquinolines
Topotecan pharmacokinetics
Subjects
Details
- Language :
- English
- ISSN :
- 0732-183X
- Volume :
- 20
- Issue :
- 13
- Database :
- MEDLINE
- Journal :
- Journal of clinical oncology : official journal of the American Society of Clinical Oncology
- Publication Type :
- Academic Journal
- Accession number :
- 12089223
- Full Text :
- https://doi.org/10.1200/JCO.2002.12.116