Literature DB >> 11990713

Phase I study of irinotecan in pediatric patients with malignant solid tumors.

Hideo Mugishima1, Tadashi Matsunaga, Keiko Yagi, Keiko Asami, Jun-ichi Mimaya, Sachiyo Suita, Tomoko Kishimoto, Tadashi Sawada, Yoshiaki Tsuchida, Michio Kaneko.   

Abstract

PURPOSE: To determine the dose-limiting toxicity, maximum tolerated dose, and potential efficacy of irinotecan in children with refractory malignant solid tumors. PATIENTS AND METHODS: In the present phase I clinical trial, 28 patients received irinotecan 50 to 200 mg/m2 per day by intravenous 2-hour infusion over the course of 3 days, repeated once after an interval of 25 days. Fifty-one treatment courses were administered to these patients.
RESULTS: Dose-limiting toxicities were observed at the dose of 200 mg/m2 per day for 3 days. Diarrhea and hematopoietic toxicities were the dose-limiting factors, and the former required support with intravenous fluid administration. The occurrence of vomiting was variable. Decreases in clinical tumor marker levels were observed in the majority of patients who received two cycles of irinotecan 80 mg/m2 per day to 200 mg/m2 per day over the course of 3 days, and partial response was attained in four patients who received irinotecan in two cycles of 140 mg/m2 per day to 200 mg/m2 per day over the course of 3 days. Pharmacokinetic studies showed that the plasma concentration of irinotecan and its active metabolite SN-38 ranged from 93 to 2,820 ng/mL and 5.2 to 34.8 ng/mL, respectively, during 3-day infusions of irinotecan 200 mg/m2 per day. The mean clearance of irinotecan was 14.54 L/h per m2 (range 8.45-20.83 L/h per m2).
CONCLUSION: The maximum tolerated dose was determined to be a dose of irinotecan between 160 mg/m2 per day and 180 mg/m2 per day administered over the course of 3 consecutive days on an inpatient basis, repeated once after 25 days off, and our results indicate that irinotecan is a promising anticancer agent that is worthy of phase II trials in pediatric solid tumors.

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Year:  2002        PMID: 11990713     DOI: 10.1097/00043426-200202000-00007

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  8 in total

1.  Phase I dose escalation and pharmacokinetic study of oral gefitinib and irinotecan in children with refractory solid tumors.

Authors:  R C Brennan; W Furman; S Mao; J Wu; D C Turner; C F Stewart; V Santana; L M McGregor
Journal:  Cancer Chemother Pharmacol       Date:  2014-09-26       Impact factor: 3.333

2.  Phase II study of irinotecan and temozolomide in children with relapsed or refractory neuroblastoma: a Children's Oncology Group study.

Authors:  Rochelle Bagatell; Wendy B London; Lars M Wagner; Stephan D Voss; Clinton F Stewart; John M Maris; Cynthia Kretschmar; Susan L Cohn
Journal:  J Clin Oncol       Date:  2010-11-29       Impact factor: 44.544

3.  Phase I trial of oral irinotecan and temozolomide for children with relapsed high-risk neuroblastoma: a new approach to neuroblastoma therapy consortium study.

Authors:  Lars M Wagner; Judith G Villablanca; Clinton F Stewart; Kristine R Crews; Susan Groshen; C Patrick Reynolds; Julie R Park; John M Maris; Randall A Hawkins; Heike E Daldrup-Link; Hollie A Jackson; Katherine K Matthay
Journal:  J Clin Oncol       Date:  2009-01-26       Impact factor: 44.544

4.  Phase 1 study of oxaliplatin and irinotecan in pediatric patients with refractory solid tumors: a children's oncology group study.

Authors:  Lisa M McGregor; Sheri L Spunt; Wayne L Furman; Clinton F Stewart; Paula Schaiquevich; Mark D Krailo; Roseanne Speights; Percy Ivy; Peter C Adamson; Susan M Blaney
Journal:  Cancer       Date:  2009-04-15       Impact factor: 6.860

5.  Tyrosine kinase inhibitor enhances the bioavailability of oral irinotecan in pediatric patients with refractory solid tumors.

Authors:  Wayne L Furman; Fariba Navid; Najat C Daw; M Beth McCarville; Lisa M McGregor; Sheri L Spunt; Carlos Rodriguez-Galindo; John C Panetta; Kristine R Crews; Jianrong Wu; Amar J Gajjar; Peter J Houghton; Victor M Santana; Clinton F Stewart
Journal:  J Clin Oncol       Date:  2009-08-17       Impact factor: 44.544

6.  Current treatment and future directions in neuroblastoma.

Authors:  Yoshiaki Tsuchida; Toshiji Shitara; Minoru Kuroiwa; Hitoshi Ikeda
Journal:  Indian J Pediatr       Date:  2003-10       Impact factor: 1.967

Review 7.  Do pharmacokinetic polymorphisms explain treatment failure in high-risk patients with neuroblastoma?

Authors:  Francesco Bellanti; Bertil Kågedal; Oscar Della Pasqua
Journal:  Eur J Clin Pharmacol       Date:  2011-02-02       Impact factor: 2.953

8.  Irinotecan metabolite SN38 results in germ cell loss in the testis but not in the ovary of prepubertal mice.

Authors:  Federica Lopes; Rowena Smith; Sophie Nash; Rod T Mitchell; Norah Spears
Journal:  Mol Hum Reprod       Date:  2016-07-28       Impact factor: 4.025

  8 in total

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