Literature DB >> 16369989

Phase II study of a protracted irinotecan schedule in children with refractory or recurrent soft tissue sarcoma.

Gianni Bisogno1, Riccardo Riccardi, Antonio Ruggiero, Giampaolo Arcamone, Arcangelo Prete, Gianmarco Surico, Massimo Provenzi, Patrizia Bertolini, Paolo Paolucci, Modesto Carli.   

Abstract

BACKGROUND: Irinotecan (CPT-11) is a novel antineoplastic agent that takes effect by inhibiting topoisomerase I. The Italian Soft Tissue Sarcoma (STS) Committee performed a multiinstitutional Phase II study to evaluate its effect on STS.
METHODS: Over a 2-year period between 2002 and 2004, 32 heavily pretreated patients were administered 60-minute infusions of irinotecan at 20 mg/m2/day, for 5 days a week, for 2 consecutive weeks. The courses were repeated every 4 weeks for at least 2 courses, unless there were signs of toxicity or disease progression. Thirty patients, 13 with peripheral primitive neuroectodermal tumor (PNET), 12 with rhabdomyosarcoma (RMS), 3 with desmoplastic small round cell tumor (DSRCT), and 2 with other STS were evaluable for response.
RESULTS: A total of 79 cycles were delivered. The main regimen-related toxicity was diarrhea, occurring in 58% of cycles with 9 episodes graded as 3 or 4. Grade 3-4 neutropenia was recorded in 10% of cycles. The overall response rate was 23% (2 complete remissions +5 partial remissions of 30 patients), 38% for PNET and 16% for RMS. In addition, 4 minor responses were noted.
CONCLUSIONS: As a single agent in the treatment of recurrent and refractory STS, irinotecan administered on a daily x5 x2 schedule revealed a noteworthy response rate in a population of heavily pretreated patients, especially in the subset of patients with PNET. Its hematologic toxicity profile warrants further investigation in association with other myelotoxic agents. Copyright (c) 2005 American Cancer Society.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16369989     DOI: 10.1002/cncr.21629

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  16 in total

1.  Phase I and Phase II Objective Response Rates are Correlated in Pediatric Cancer Trials: An Argument for Better Clinical Trial Efficiency.

Authors:  Jonathan C Yeh; Peng Huang; Kenneth J Cohen
Journal:  J Pediatr Hematol Oncol       Date:  2016-07       Impact factor: 1.289

2.  The use of interval-compressed chemotherapy with the addition of vincristine, irinotecan, and temozolomide for pediatric patients with newly diagnosed desmoplastic small round cell tumor.

Authors:  Kevin X Liu; Natalie B Collins; Katie A Greenzang; Elissa Furutani; Kevin Campbell; Andrew Groves; Elizabeth A Mullen; Suzanne Shusterman; Jennifer Spidle; Karen J Marcus; Brent R Weil; Christopher B Weldon; A Lindsay Frazier; Katherine A Janeway; Allison F O'Neill; Jennifer W Mack; Steven G DuBois; David S Shulman
Journal:  Pediatr Blood Cancer       Date:  2020-07-19       Impact factor: 3.167

3.  Dose escalation of intravenous irinotecan using oral cefpodoxime: a phase I study in pediatric patients with refractory solid tumors.

Authors:  Lisa M McGregor; Clinton F Stewart; Kristine R Crews; Michael Tagen; Amy Wozniak; Jianrong Wu; M Beth McCarville; Fariba Navid; Victor M Santana; Peter J Houghton; Wayne L Furman; Carlos Rodriguez-Galindo
Journal:  Pediatr Blood Cancer       Date:  2011-04-20       Impact factor: 3.167

4.  Topotecan plus cyclophosphamide in adults with relapsed or refractory pediatric-type sarcoma: a retrospective analysis from the German Sarcoma Medical Oncology Group (AIO).

Authors:  Jörg Thomas Hartmann; R D Issels; K San Nicolo; V Grünwald; B Hertenstein; E Papesch; S Krause; I Sturm
Journal:  Invest New Drugs       Date:  2015-07-12       Impact factor: 3.850

5.  Metastatic desmoplastic small round cell tumor controlled by an anthracycline-based regimen: review of the role of chemotherapy.

Authors:  H Mrabti; W Kaikani; N Ahbeddou; H Abahssain; B El Khannoussi; M Amrani; H Errihani
Journal:  J Gastrointest Cancer       Date:  2012-03

Review 6.  Neurotoxicity of chemotherapeutic and biologic agents in children with cancer.

Authors:  Kevin C De Braganca; Roger J Packer
Journal:  Curr Neurol Neurosci Rep       Date:  2008-03       Impact factor: 5.081

7.  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

8.  Phase I trial of two schedules of vincristine, oral irinotecan, and temozolomide (VOIT) for children with relapsed or refractory solid tumors: a Children's Oncology Group phase I consortium study.

Authors:  Lars M Wagner; John P Perentesis; Joel M Reid; Matthew M Ames; Stephanie L Safgren; Marvin D Nelson; Ashish M Ingle; Susan M Blaney; Peter C Adamson
Journal:  Pediatr Blood Cancer       Date:  2010-04       Impact factor: 3.167

Review 9.  Prospects and challenges for the development of new therapies for Ewing sarcoma.

Authors:  Patrick J Grohar; Lee J Helman
Journal:  Pharmacol Ther       Date:  2012-10-18       Impact factor: 12.310

10.  Camptothecin-based regimens for treatment of ewing sarcoma: past studies and future directions.

Authors:  Lars Wagner
Journal:  Sarcoma       Date:  2011-04-06
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.