Clinical Trial: Study of PEG-Intron for Plexiform Neurofibromas
Study Status: Active, not recruiting
Recruit Status: Active, not recruiting
Study Type: Interventional
Official Title: A Phase II Trial of Peginterferon Alfa-2b (PEG-Intron) for Plexiform Neurofibromas
Brief Summary:
This study is for slow growing tumors called plexiform neurofibromas (PNF) which are a relatively common problem in people with neurofibromatosis type 1 (NF1). These tumors are benign but as they grow, they can become disfiguring as well as disabling or even life threatening. They often cause pain, difficulty using arms or legs because of spinal cord compression, and/or nerve damage. At present, the only available therapy for plexiform neurofibromas is to try to surgically remove as much of the tumor as is possible. Because these tumors grow into the surrounding areas, total surgical resection is often impossible. Most tumors will re-grow after surgery if the entire tumor cannot be removed. To date, other treatments including chemotherapy and radiotherapy have not been able to shrink these tumors.
Interferon is a drug that is used for different types of tumors as well as for hepatitis. It has been used in the treatment of plexiform neurofibromas (PNF) with some subjects showing improvement in symptoms and/or a decrease in the size of the tumor. Most subjects had no further growth of their tumor while on the PEG-Intron. The drug used in this study is PEG (pegylated)-Intron. PEG-Intron is a long acting form of interferon which keeps the drug from being broken down in the body for a longer period of time and potentially could be more effective than the short-acting interferon. PEG-Intron has been approved by the Food and Drug Administration (FDA) for the treatment of Hepatitis C.
The goals of this study are:
- To determine how your child's plexiform neurofibroma responds to PEG-Intron when given weekly.
- To determine the side effects of PEG-Intron when given weekly to participants with plexiform neurofibromas.
Detailed Summary:
PEG-Intron will be given every week through a small needle under the skin, in the same way that insulin is given to people with diabetes. Subjects will be taught to do this at home. As long as the tumor isn't growing and the side effects are tolerable, the injections will be given once a week for 2 years.
Children will be enrolled on the study into one of three strata (patient groups): strata 1 includes children who do not have any symptoms associated with their PNF and MRI scans over the past year may or may not show tumor growth, strata 2 includes children who have symptoms associated with the PNF but MRI scans over the past year have not shown growth and strata 3 includes children who have shown an increase in the size of the PNF on MRI scans over the past year, with or without any symptoms.
Sponsor: University of Pittsburgh
Current Primary Outcome: The primary outcomes for the the study will be response or progression free survival, depending on the stratum in which the patient has enrolled. [ Time Frame: 5 years ]
Original Primary Outcome: The primary outcomes for the the study will be response or progression free survival, depending on the stratum in which the patient has enrolled.
Current Secondary Outcome:
Original Secondary Outcome:
Information By: University of Pittsburgh
Dates:
Date Received: November 2, 2006
Date Started: November 2006
Date Completion: November 2017
Last Updated: February 24, 2016
Last Verified: February 2016
