Literature DB >> 14752800

Phase I study of oral cyclophosphamide and oral topotecan for children with recurrent or refractory solid tumors.

Daniel C Bowers1, Victor M Aquino, Patrick J Leavey, Robert O Bash, Janna M Journeycake, Gail Tomlinson, Arlynn F Mulne, Heidi J Haynes, Naomi J Winick.   

Abstract

BACKGROUND: To determine the maximum-tolerated duration and dose-limiting toxicity of a daily schedule of orally administered cyclophosphamide and topotecan in pediatric patients with recurrent or refractory malignant solid tumors.
METHODS: Patients received oral cyclophosphamide (50 mg/m2/dose) in the morning followed by topotecan (0.8 mg/m2/dose) 8-12 hr later for an escalating number of consecutive days (10, 14, and 17 days).
RESULTS: Seventeen pediatric patients were treated with oral cyclophosphamide and topotecan for durations of 10-17 days for a total of 58 treatment courses. Reversible hematologic toxicity (neutropenia and thrombocytopenia) was the dose-limiting toxicity. Nonhematologic toxicities of greater than grade 3 were not observed. A partial response (neuroblastoma following myeloablative chemotherapy and stem cell rescue) and prolonged stable disease (medulloblastoma) were each observed in one patient.
CONCLUSIONS: The recommended duration of therapy with a daily schedule of both oral cyclophosphamide (50 mg/m2/day) and topotecan (0.8 mg/m2/day) for previously treated pediatric patients with recurrent or refractory solid tumors is 14 consecutive days. The observed dose limiting toxicity (DLT) was reversible neutropenia. This regimen was well tolerated in heavily pretreated patients and demonstrated activity against recurrent pediatric solid tumors. Copyright 2003 Wiley-Liss, Inc.

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Year:  2004        PMID: 14752800     DOI: 10.1002/pbc.10456

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  5 in total

1.  Risk-adapted therapy for young children with medulloblastoma (SJYC07): therapeutic and molecular outcomes from a multicentre, phase 2 trial.

Authors:  Giles W Robinson; Vasilisa A Rudneva; Ivo Buchhalter; Catherine A Billups; Sebastian M Waszak; Kyle S Smith; Daniel C Bowers; Anne Bendel; Paul G Fisher; Sonia Partap; John R Crawford; Tim Hassall; Daniel J Indelicato; Frederick Boop; Paul Klimo; Noah D Sabin; Zoltan Patay; Thomas E Merchant; Clinton F Stewart; Brent A Orr; Jan O Korbel; David T W Jones; Tanvi Sharma; Peter Lichter; Marcel Kool; Andrey Korshunov; Stefan M Pfister; Richard J Gilbertson; Robert P Sanders; Arzu Onar-Thomas; David W Ellison; Amar Gajjar; Paul A Northcott
Journal:  Lancet Oncol       Date:  2018-05-16       Impact factor: 41.316

2.  Stability of cyclophosphamide in extemporaneous oral suspensions.

Authors:  Rachel Kennedy; Daniel Groepper; Michael Tagen; Robbin Christensen; Fariba Navid; Amar Gajjar; Clinton F Stewart
Journal:  Ann Pharmacother       Date:  2010-01-26       Impact factor: 3.154

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

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

4.  Phase 1 study of sirolimus in combination with oral cyclophosphamide and topotecan in children and young adults with relapsed and refractory solid tumors.

Authors:  Kieuhoa T Vo; Erin E Karski; Nicole M Nasholm; Shelly Allen; Fabienne Hollinger; W Clay Gustafson; Janel R Long-Boyle; Stephen Shiboski; Katherine K Matthay; Steven G DuBois
Journal:  Oncotarget       Date:  2017-04-04

Review 5.  Medulloblastoma in children and adolescents: a systematic review of contemporary phase I and II clinical trials and biology update.

Authors:  Francisco Bautista; Victoria Fioravantti; Teresa de Rojas; Fernando Carceller; Luis Madero; Alvaro Lassaletta; Lucas Moreno
Journal:  Cancer Med       Date:  2017-10-04       Impact factor: 4.452

  5 in total

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