Literature DB >> 7720181

Pharmacokinetics of irinotecan and its metabolites in human blood, bile, and urine.

F Lokiec1, P Canal, C Gay, E Chatelut, J P Armand, H Roché, R Bugat, E Gonçalvès, A Mathieu-Boué.   

Abstract

Two patients were treated with CPT-11 for colorectal cancer and had a percutaneous biliary catheter for extrahepatic biliary obstruction. The first patient was treated with CPT-11 according to the 100-mg/m2 weekly therapeutic schedule, and the second patient was treated every 3 weeks, with a dose of 350 mg/m2 being given at the first course, after which it was decreased to 300 mg/m2 for the following courses. In plasma, the active identified metabolite of CPT-11, SN-38, occurred mainly in the form of a glucuronide conjugate. CPT-11 was mainly excreted in bile and urine as CPT-11. The cumulative biliary and urinary excretion of CPT-11 and its metabolites (SN-38 and SN-38 glucuronide conjugate) over a period of up to 48 h ranged from 25% (100 mg/m2 weekly) to 50% (300 mg/m2 every 3 weeks). This means that CPT-11 can be excreted under other, not yet identified metabolite forms.

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Year:  1995        PMID: 7720181     DOI: 10.1007/BF00685737

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  7 in total

1.  Simultaneous determination of the camptothecin analogue CPT-11 and its active metabolite SN-38 by high-performance liquid chromatography: application to plasma pharmacokinetic studies in cancer patients.

Authors:  I Barilero; D Gandia; J P Armand; A Mathieu-Boué; M Ré; A Gouyette; G G Chabot
Journal:  J Chromatogr       Date:  1992-03-27

2.  Synthesis of water-soluble (aminoalkyl)camptothecin analogues: inhibition of topoisomerase I and antitumor activity.

Authors:  W D Kingsbury; J C Boehm; D R Jakas; K G Holden; S M Hecht; G Gallagher; M J Caranfa; F L McCabe; L F Faucette; R K Johnson
Journal:  J Med Chem       Date:  1991-01       Impact factor: 7.446

3.  Phase I and pharmacokinetic trial of weekly CPT-11.

Authors:  M L Rothenberg; J G Kuhn; H A Burris; J Nelson; J R Eckardt; M Tristan-Morales; S G Hilsenbeck; G R Weiss; L S Smith; G I Rodriguez
Journal:  J Clin Oncol       Date:  1993-11       Impact factor: 44.544

4.  Intracellular roles of SN-38, a metabolite of the camptothecin derivative CPT-11, in the antitumor effect of CPT-11.

Authors:  Y Kawato; M Aonuma; Y Hirota; H Kuga; K Sato
Journal:  Cancer Res       Date:  1991-08-15       Impact factor: 12.701

5.  Identification and kinetics of a beta-glucuronide metabolite of SN-38 in human plasma after administration of the camptothecin derivative irinotecan.

Authors:  L P Rivory; J Robert
Journal:  Cancer Chemother Pharmacol       Date:  1995       Impact factor: 3.333

6.  Nonlinear pharmacokinetics of CPT-11 in rats.

Authors:  N Kaneda; T Yokokura
Journal:  Cancer Res       Date:  1990-03-15       Impact factor: 12.701

7.  Metabolism and pharmacokinetics of the camptothecin analogue CPT-11 in the mouse.

Authors:  N Kaneda; H Nagata; T Furuta; T Yokokura
Journal:  Cancer Res       Date:  1990-03-15       Impact factor: 12.701

  7 in total
  9 in total

Review 1.  Clinical pharmacokinetics of irinotecan.

Authors:  G G Chabot
Journal:  Clin Pharmacokinet       Date:  1997-10       Impact factor: 6.447

Review 2.  Liposomal Irinotecan: A Review in Metastatic Pancreatic Adenocarcinoma.

Authors:  Yvette N Lamb; Lesley J Scott
Journal:  Drugs       Date:  2017-05       Impact factor: 9.546

3.  Reduced gastrointestinal toxicity following inhibition of the biliary excretion of irinotecan and its metabolites by probenecid in rats.

Authors:  Masato Horikawa; Yukio Kato; Yuichi Sugiyama
Journal:  Pharm Res       Date:  2002-09       Impact factor: 4.200

Review 4.  Organic Anion Transporting Polypeptides: Emerging Roles in Cancer Pharmacology.

Authors:  Rachael R Schulte; Richard H Ho
Journal:  Mol Pharmacol       Date:  2019-02-19       Impact factor: 4.436

Review 5.  Therapeutic targeting of CPT-11 induced diarrhea: a case for prophylaxis.

Authors:  Umang Swami; Sanjay Goel; Sridhar Mani
Journal:  Curr Drug Targets       Date:  2013-06       Impact factor: 3.465

6.  Clinical usefulness of testing for UDP glucuronosyltransferase 1 family, polypeptide A1 polymorphism prior to the inititation of irinotecan-based chemotherapy.

Authors:  Taishi Harada; Haruhiro Saito; Fumi Karino; Tetsuya Isaka; Shuji Murakami; Tetsuro Kondo; Fumihiro Oshita; Yohei Miyagi; Kouzo Yamada
Journal:  Mol Clin Oncol       Date:  2014-06-06

Review 7.  Camptothecin and podophyllotoxin derivatives: inhibitors of topoisomerase I and II - mechanisms of action, pharmacokinetics and toxicity profile.

Authors:  Jörg T Hartmann; Hans-Peter Lipp
Journal:  Drug Saf       Date:  2006       Impact factor: 5.606

8.  A risk-benefit assessment of irinotecan in solid tumours.

Authors:  L L Siu; E K Rowinsky
Journal:  Drug Saf       Date:  1998-06       Impact factor: 5.606

9.  In vitro chemotherapy-associated muscle toxicity is attenuated with nutritional support, while treatment efficacy is retained.

Authors:  Liza A Wijler; Francina J Dijk; Hanil Quirindongo; Danielle A E Raats; Bram Dorresteijn; Matthew J W Furber; Anne M May; Onno Kranenburg; Miriam van Dijk
Journal:  Oncotarget       Date:  2022-10-08
  9 in total

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