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Study of Plexiform Neurofibromas in Neurofibromatosis Type 1

Natural History of Plexiform in Neurofibromatosis Type I

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00006435
Enrollment
24
Registered
2000-11-06
Start date
2001-05-18
Completion date
2020-05-01
Last updated
2020-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

NF1, Plexiform Neurofibromas

Keywords

Tissue Repository, Growth Rate, Volumetric MRI

Brief summary

Background: -Plexiform neurofibromas in patients with NF1 are a significant cause of morbidity but little is known about the natural history of these lesions. Objectives: * The purpose of this study is to monitor the natural history of plexiform neurofibromas and to evaluate the usefulness of volumetric MRI tumor measurements in this disease. * Other goals of the study are to provide a body of normative data on the growth rate of plexiform neurofibromas and to establish a tissue repository and pathology review center to allow future studies of the pathogenesis of neurofibromas and clinical trials of potential therapeutic agents. Design \- This study is coordinated by Dr. Bruce Korf, and was initiated when he was at the Partners Center for Human Genetics, Boston, MA.

Detailed description

Background: -Plexiform neurofibromas in patients with NF1 are a significant cause of morbidity but little is known about the natural history of these lesions. Objectives: * The purpose of this study is to monitor the natural history of plexiform neurofibromas and to evaluate the usefulness of volumetric MRI tumor measurements in this disease. * Other goals of the study are to provide a body of normative data on the growth rate of plexiform neurofibromas and to establish a tissue repository and pathology review center to allow future studies of the pathogenesis of neurofibromas and clinical trials of potential therapeutic agents. Design \- This study is coordinated by Dr. Bruce Korf, and was initiated when he was at the Partners Center for Human Genetics, Boston, MA.

Interventions

None listed

Sponsors

National Cancer Institute (NCI)
Lead SponsorNIH

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 100 Years
Healthy volunteers
No

Inclusion criteria

* INCLUSION * Diagnosis of Neurofibromatosis: All study subjects will fulfill two or more of the diagnostic criteria listed below for NF1. * Six or more caf(SqrRoot)(Copyright)-au-lait macules * 1.5cm or larger in postpubertal individuals * 0.5 cm or larger in prepubertal individuals * Two or more neurofibromas of any type or 1 or more plexiform neurofibroma * Freckling in the axilla or groin * Optic glioma (tumor of the optic pathway) * Two or more Lisch nodules (benign iris hamartomas) * A distinctive bony lesion * Dysplasia of the sphenoid bone * Dysplasia or thinning of long bone cortex * A first degree relative with NF-1 * Plexiform Neurofibroma: A plexiform neurofibroma fulfilling entry criteria for the study will be defined as a diffuse soft tissue or nerve enlargement in a patient with NF1 that is causing, or has potential to cause, disfigurement or functional disability. * Distribution of Plexiform Neurofibromas by site: A total of 300 plexiform neurofibromas will be studied, consisting of 100 tumors in the following three groups (based on region of maximal involvement): * Head and Neck * Trunk and Limbs (externally visible) * Trunk and Limbs (internal) \[spinal plexiform neurofibromas involve two or more levels with connection between the levels or extending laterally along the nerve\] * Subject Ascertainment: Study subjects will be ascertained at any of the participating clinical centers. It is expected that these will include subjects already followed in these clinics, as well as newly diagnosed patients EXCLUSION * Presence of metallic implant(s) that will make the patient unable to have MRI studies * Presence of medical or psychological condition that will make the patient unable to tolerate MRI studies or anesthesia (if needed) * Inability to image tumor or define tumor margins by MRI (which may be determined after the initial study) * Failure to obtain initial MRI within 60 days of enrollment * Previous radiation therapy to site of plexiform neurofibroma * Surgery involving the plexiform neurofibroma (excluding biopsy) within a six month period before enrollment * Current antineoplastic therapy * Entry of more than one member of the same family into the study is not permitted

Design outcomes

Primary

MeasureTime frameDescription
Monitor natural history of plexiform neurofibromas3 yearsMonitor natural history of plexiform neurofibromas
Usefulness of volumetric MRI measurements4 yearsUsefulness of volumetric MRI measurements

Secondary

MeasureTime frame
Establish tissue repository & pathology reviews center3 years
Body of data regarding growth rate of plexiform neurofibromas3 years

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026