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| Sponsors and Collaborators: |
Children's Oncology Group National Cancer Institute (NCI) |
|---|---|
| Information provided by: | National Cancer Institute (NCI) |
| ClinicalTrials.gov Identifier: | NCT00003793 |
Purpose
RATIONALE: Determination of genetic markers for soft tissue sarcoma or rhabdomyosarcoma may help doctors identify patients who are at risk for therapy-related leukemia.
PURPOSE: Clinical trial to study genetic testing of children with soft tissue sarcoma or rhabdomyosarcoma to identify children who are at risk of developing leukemia from the chemotherapy used to treat sarcoma.
| Condition | Intervention |
|---|---|
|
Leukemia Myelodysplastic Syndromes Sarcoma |
Genetic: clonality analysis Genetic: microsatellite instability analysis Genetic: mutation analysis |
| Study Type: | Observational |
| Official Title: | Clinical and Biological Predictors of Therapy-Related Leukemia |
| Estimated Enrollment: | 321 |
| Study Start Date: | December 1998 |
OBJECTIVES:
OUTLINE: Blood is collected from patients at diagnosis (preferably before chemotherapy or transfusion), at end of therapy, and at 6 months, 1 year, 2 years, and 3 years after therapy.
Blood specimens are examined by clonality analysis (HUMARA), variant cell frequency (glycophorin A assay), GST NAT2/CYP1A1 genotyping, microsatellite instability, and ras mutation detection (single strand conformation polymorphism and sequencing of mutant alleles).
Patients do not receive the results of the genetic testing and the results do not influence the type or duration of treatment.
PROJECTED ACCRUAL: A total of 321 patients will be accrued for this study within 4 years.
Eligibility| Ages Eligible for Study: | up to 17 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
DISEASE CHARACTERISTICS:
Diagnosis of sarcoma including:
PATIENT CHARACTERISTICS:
Age:
Performance status:
Life expectancy:
Hematopoietic:
Hepatic:
Renal:
PRIOR CONCURRENT THERAPY:
Biologic therapy
Chemotherapy
Endocrine therapy
Radiotherapy
Surgery
Contacts and Locations
Show 96 Study Locations| Study Chair: | Stella M. Davies, MBBS, PhD | Children's Hospital Medical Center, Cincinnati |
More Information
| Study ID Numbers: | CDR0000066936, COG-AB9804, CCG-B9804 |
| Study First Received: | November 1, 1999 |
| Last Updated: | February 6, 2009 |
| ClinicalTrials.gov Identifier: | NCT00003793 History of Changes |
| Health Authority: | United States: Federal Government |
|
secondary acute myeloid leukemia secondary myelodysplastic syndromes localized osteosarcoma metastatic osteosarcoma childhood soft tissue sarcoma nonmetastatic childhood soft tissue sarcoma metastatic childhood soft tissue sarcoma |
childhood fibrosarcoma childhood synovial sarcoma childhood neurofibrosarcoma previously untreated childhood rhabdomyosarcoma localized Ewing sarcoma/peripheral primitive neuroectodermal tumor metastatic Ewing sarcoma/peripheral primitive neuroectodermal tumor |
|
Fibrosarcoma Neuroectodermal Tumors, Primitive Precancerous Conditions Leukemia, Myeloid, Acute Sarcoma, Synovial Leukemia Neoplasms, Connective and Soft Tissue Sarcoma, Ewing's Preleukemia Soft Tissue Sarcomas Acute Myelocytic Leukemia Neoplasm Metastasis Neuroepithelioma Osteogenic Sarcoma Synovial Sarcoma |
Ewing's Family of Tumors Rhabdomyosarcoma Hematologic Diseases Myelodysplastic Syndromes Osteosarcoma Rhabdomyosarcoma, Childhood Leukemia, Myeloid Ewing's Sarcoma Neuroectodermal Tumors Malignant Mesenchymal Tumor Peripheral Neuroectodermal Tumor Sarcoma Bone Marrow Diseases Neuroectodermal Tumors, Primitive, Peripheral |
|
Neoplasms, Muscle Tissue Disease Neoplasms by Histologic Type Precancerous Conditions Hematologic Diseases Myosarcoma Myelodysplastic Syndromes Neoplasms, Connective and Soft Tissue |
Leukemia Preleukemia Neoplasms Pathologic Processes Syndrome Sarcoma Bone Marrow Diseases Rhabdomyosarcoma |
