Completed

A Phase II Study of Continuous 21 Day Infusion of Topotecan (NSC # 609699) in Children With Relapsed Solid Tumors

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What is being tested

topotecan hydrochloride

Drug
Who is being recruted

Neoplasms+11

+ Neoplasms by Histologic Type

+ Neoplasms, Connective Tissue

Until 21 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Phase 2
Interventional
Study Start: May 1999
See protocol details

Summary

Principal SponsorNational Cancer Institute (NCI)
Last updated: February 5, 2013
Sourced from a government-validated database.Claim as a partner

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.

NCT00003745
Principal SponsorNational Cancer Institute (NCI)
Last updated: February 5, 2013
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

125 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

NeoplasmsNeoplasms by Histologic TypeNeoplasms, Connective TissueNeoplasms, Germ Cell and EmbryonalNeoplasms, Glandular and EpithelialNeoplasms, Nerve TissueNeuroectodermal TumorsNeoplasms, Connective and Soft TissueNeoplasms, Bone TissueNeuroectodermal Tumors, PrimitiveNeoplasms, NeuroepithelialSarcomaOsteosarcomaNeuroectodermal Tumors, Primitive, Peripheral

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.
Treatment Groups

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
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.

Study 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 Maps

University of South Alabama Medical Center

Mobile, United States

Phoenix Children's Hospital

Phoenix, United States

Arizona Cancer Center

Tucson, United States
Completed235 Study Centers