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| Sponsor: | Children's Hospital of Philadelphia |
|---|---|
| Information provided by: | National Cancer Institute (NCI) |
| ClinicalTrials.gov Identifier: | NCT00030264 |
Purpose
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining methotrexate with vinblastine may be effective treatment for neurofibromatosis type 1 associated with progressive plexiform neurofibromas.
PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy in treating patients who have neurofibromatosis type 1 associated with progressive plexiform neurofibromas.
| Condition | Intervention | Phase |
|---|---|---|
|
Neurofibromatosis Type 1 Precancerous Condition |
Drug: methotrexate Drug: vinblastine sulfate |
Phase II |
| Study Type: | Interventional |
| Study Design: | Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Vinblastine/Methotrexate For Severe Progressive Plexiform Neurofibromas: A Phase II Study |
| Estimated Enrollment: | 35 |
| Study Start Date: | February 2001 |
| Estimated Primary Completion Date: | December 2011 (Final data collection date for primary outcome measure) |
OBJECTIVES:
OUTLINE: Patients are stratified according to tumor status (severely debilitating and/or life-threatening vs cosmetically disfiguring).
Patients receive methotrexate and vinblastine IV weekly for 26 weeks and then every 2 weeks for 26 weeks in the absence of disease progression or unacceptable toxicity.
Quality of life is assessed at baseline and then every 3 months during study participation.
Patients are followed every 3 months until disease progression.
PROJECTED ACCRUAL: A total of 35 patients will be accrued for this study within approximately 3 years.
Eligibility| Ages Eligible for Study: | up to 25 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
DISEASE CHARACTERISTICS:
Diagnosis of progressive, debilitating, severely disfiguring, or life-threatening plexiform neurofibroma (PN) that is surgically unresectable (or surgery refused by patient) and for which there is no other standard medical management
Histologic confirmation of tumor not required in the presence of consistent clinical and radiographic findings
Measurable disease
Recurrent or progressive disease as documented by an increase in size or the presence of new lesions on MRI
Must meet at least one other diagnostic criteria for neurofibromatosis type 1 (NF1):
PATIENT CHARACTERISTICS:
Age:
Performance status:
Life expectancy:
Hematopoietic:
CBC normal
Hepatic:
Renal:
Other:
PRIOR CONCURRENT THERAPY:
Biologic therapy:
Chemotherapy:
Endocrine therapy:
Radiotherapy:
Surgery:
Other:
Contacts and Locations| United States, Pennsylvania | |
| Children's Hospital of Philadelphia | Recruiting |
| Philadelphia, Pennsylvania, United States, 19104 | |
| Contact: Jean B. Belasco, MD 215-590-3129 | |
| Study Chair: | Jean B. Belasco, MD | Children's Hospital of Philadelphia |
More Information
| Responsible Party: | Jean Bello Belasco, Children's Hospital of Philadelphia |
| ClinicalTrials.gov Identifier: | NCT00030264 History of Changes |
| Other Study ID Numbers: | CDR0000069065, CHP-686, CHP-IRB-2001-2-2339, NCI-V01-1678 |
| Study First Received: | February 14, 2002 |
| Last Updated: | November 2, 2010 |
| Health Authority: | Unspecified |
|
plexiform neurofibroma neurofibromatosis type 1 |
|
Disease Neurofibroma Neurofibromatosis 1 Osteitis Fibrosa Cystica Precancerous Conditions Neurofibromatoses Neurofibroma, Plexiform Pathologic Processes Nerve Sheath Neoplasms Neoplasms, Nerve Tissue Neoplasms by Histologic Type Neoplasms Peripheral Nervous System Neoplasms Nervous System Neoplasms Nervous System Diseases |
Peripheral Nervous System Diseases Neuromuscular Diseases Neoplastic Syndromes, Hereditary Neurocutaneous Syndromes Heredodegenerative Disorders, Nervous System Neurodegenerative Diseases Genetic Diseases, Inborn Bone Diseases, Endocrine Bone Diseases Musculoskeletal Diseases Methotrexate Vinblastine Abortifacient Agents, Nonsteroidal Abortifacient Agents Reproductive Control Agents |