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Population pharmacokinetics of intraperitoneal irinotecan and SN-38 in patients with peritoneal metastases from colorectal origin.
- Source :
-
CPT: pharmacometrics & systems pharmacology [CPT Pharmacometrics Syst Pharmacol] 2024 Jun; Vol. 13 (6), pp. 1006-1016. Date of Electronic Publication: 2024 Apr 17. - Publication Year :
- 2024
-
Abstract
- Peritoneal metastases (PM) are common in patients with colorectal cancer. Patients with PM have a poor prognosis, and for those who are not eligible for cytoreductive surgery (CRS) with or without hyperthermic intraperitoneal chemotherapy (HIPEC), palliative chemotherapy is currently the only option. Recently, we conducted a phase I trial (INTERACT) in which irinotecan was administered intraperitoneally (IP) to 18 patients ineligible for CRS-HIPEC. The primary objective was to evaluate covariates influencing the PK profile of irinotecan and SN-38 after IP administration. Secondly, a population PK model was developed to support the further development of IP irinotecan by improving dosing in patients with PM. Patients were treated with IP irinotecan every 2 weeks in combination with systemic FOLFOX-bevacizumab. Irinotecan and SN-38 were measured in plasma (588 samples) and SN-38 was measured in peritoneal fluid (267 samples). Concentration-Time data were log-transformed and analyzed using NONMEM version 7.5 using FOCE+I estimation. An additive error model described the residual error, with inter-individual variability in PK parameters modeled exponentially. The final structural model consisted of five compartments. Weight was identified as a covariate influencing the SN-38 plasma volume of distribution and GGT was found to influence the SN-38 plasma clearance. This population PK model adequately described the irinotecan and SN-38 in plasma after IP administration, with weight and GGT as predictive factors. Irinotecan is converted intraperitoneal to SN-38 by carboxylesterases and the plasma bioavailability of irinotecan is low. This model will be used for the further clinical development of IP irinotecan by providing dosing strategies.<br /> (© 2024 The Authors. CPT: Pharmacometrics & Systems Pharmacology published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.)
- Subjects :
- Humans
Male
Middle Aged
Female
Aged
Adult
Camptothecin analogs & derivatives
Camptothecin pharmacokinetics
Camptothecin administration & dosage
Camptothecin therapeutic use
Models, Biological
Bevacizumab pharmacokinetics
Bevacizumab administration & dosage
Bevacizumab therapeutic use
Leucovorin pharmacokinetics
Leucovorin administration & dosage
Leucovorin therapeutic use
Fluorouracil pharmacokinetics
Fluorouracil administration & dosage
Injections, Intraperitoneal
Organoplatinum Compounds
Irinotecan pharmacokinetics
Irinotecan administration & dosage
Peritoneal Neoplasms secondary
Peritoneal Neoplasms drug therapy
Colorectal Neoplasms drug therapy
Colorectal Neoplasms pathology
Antineoplastic Combined Chemotherapy Protocols pharmacokinetics
Antineoplastic Combined Chemotherapy Protocols administration & dosage
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 2163-8306
- Volume :
- 13
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- CPT: pharmacometrics & systems pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 38634204
- Full Text :
- https://doi.org/10.1002/psp4.13136