A Phase II Study of Continuous 21 Day Infusion of Topotecan (NSC # 609699) in Children With Relapsed Solid Tumors
topotecan hydrochloride
Neoplasms+11
+ Neoplasms by Histologic Type
+ Neoplasms, Connective Tissue
Treatment Study
Summary
Study start date: May 1, 1999
Actual date on which the first participant was enrolled.OBJECTIVES: I. Determine the response rate in children with recurrent or refractory brain tumors, sarcomas, or neuroblastomas treated with topotecan. (Brain tumor and neuroblastoma strata closed to accrual effective 07/02/2001) II. Assess the toxicity of this regimen in a larger group of patients treated at the currently defined maximum tolerated dose. OUTLINE: This is a multicenter study. Patients receive topotecan IV continuously on days 1-21. Treatment continues at least every 4 weeks in the absence of unacceptable toxicity or disease progression. Patients are followed every 3 months.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.125 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Until 21 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
DISEASE CHARACTERISTICS: Histologically confirmed malignancy that is relapsed or refractory to conventional therapy at original diagnosis including: Brain tumors Gliomas or astrocytomas Medulloblastomas or primitive neuroectodermal tumor (PNET) in CNS (Brain tumor stratum closed to accrual effective 07/02/2001) Sarcomas Soft tissue sarcoma (undifferentiated sarcoma, embryonal or alveolar rhabdomyosarcoma (RMS), or non-RMS soft tissue sarcoma) Osteosarcoma Ewing's sarcoma/peripheral PNET tumors Neuroblastoma (Neuroblastoma stratum closed to accrual effective 07/02/2001) Histology requirement waived for brain stem tumors (Brain tumor stratum closed to accrual effective 07/02/2001) Measurable disease documented by clinical, radiographic, or histologic criteria Lesions in previously irradiated fields may be used to assess tumor response if there has been evidence of subsequent tumor growth in those fields No bone marrow metastases with granulocytopenia and/or thrombocytopenia PATIENT CHARACTERISTICS: Age: 30 days to 21 years at diagnosis Performance status: ECOG 0-2 Life expectancy: More than 2 months Hematopoietic: Absolute neutrophil count at least 1,000/mm3 Hemoglobin at least 10.0 g/dL (may receive RBC transfusions) Platelet count at least 100,000/mm3 (50,000/mm3 if post bone marrow transplantation) (transfusion independent) Hepatic: Bilirubin no greater than 1.5 times normal SGOT or SGPT less than 2.5 times normal Renal: Creatinine no greater than 1.5 times normal OR Creatinine clearance or radioisotope glomerular filtration rate at least 70 mL/min Neurologic: No greater than grade 2 CNS toxicity OR Stable CNS status for brain tumors (Brain tumor stratum closed to accrual effective 07/02/2001) Seizure disorders allowed if well-controlled with anticonvulsants Other: Not pregnant or nursing Negative pregnancy test Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Biologic therapy: At least 3 months since prior bone marrow transplantation and recovered At least 2 weeks since prior cytokines and recovered No concurrent filgrastim (G-CSF) or other cytokines No concurrent immunomodulating agents Chemotherapy: At least 2 weeks since prior chemotherapy (4 weeks for nitrosoureas) and recovered No prior topotecan or other camptothecins No other concurrent anticancer chemotherapy Endocrine therapy: Concurrent corticosteroids for CNS tumors with increased intracranial pressure allowed (Brain tumor stratum closed to accrual effective 07/02/2001) Radiotherapy: At least 2 months since prior craniospinal radiotherapy or radiotherapy to more than 50% of the bone marrow and recovered Concurrent radiotherapy to localized painful lesions allowed provided that at least 1 measurable lesion is not irradiated Other: Recovered from any other prior therapy
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 235 locations
University of Alabama at Birmingham Comprehensive Cancer Center
Birmingham, United StatesOpen University of Alabama at Birmingham Comprehensive Cancer Center in Google MapsUniversity of South Alabama Medical Center
Mobile, United StatesPhoenix Children's Hospital
Phoenix, United StatesArizona Cancer Center
Tucson, United States