Study of PEG-Intron for Plexiform Neurofibromas



Status:Completed
Conditions:Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:Any - 21
Updated:11/8/2017
Start Date:December 2006
End Date:April 2014

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A Phase II Trial of Peginterferon Alfa-2b (PEG-Intron) for Plexiform Neurofibromas

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:

1. To determine how your child's plexiform neurofibroma responds to PEG-Intron when given
weekly.

2. To determine the side effects of PEG-Intron when given weekly to participants with
plexiform neurofibromas.

3. To evaluate a new method of measuring changes in the size of tumors called volume
analysis. This method measures the entire volume of a tumor in three dimensions. The
standard method of measuring tumors uses only the length and/or width of the tumor. By
studying the different ways of measuring tumors the investigators hope to be able to
determine which method is the most accurate and useful.

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.

Inclusion Criteria:

- Age > or equal to 18 months to 21 years

- Diagnosis Patients with NF1 and progressive, symptomatic or life-threatening plexiform
neurofibromas which are not surgically resectable. Patients without biopsy-proof of
plexiform must have at least one other diagnostic criteria for NF1: 6 or more
cafe-au-lait spots, freckling in the axilla or groin, optic glioma, 2 or more Lisch
nodules, distinctive bony lesion, first degree relative with NF1.

- Only eligible if complete tumor resection is not feasible, or if a patient with a
surgical option refuses surgery.

- Patients may be treated on this trial without having received prior therapy. If
patients have received prior therapy, they must have recovered from all toxic effects
prior to entering this study.

- Must have life expectancy of at least 12 months and a performance score (Karnofsky or
Lansky) of > or equal to 50.

- Must have adequate liver, kidney and bone marrow function

Exclusion Criteria:

- Clinically significant unrelated systemic illness.

- Received an investigational agent within the past 30 days.

- Evidence of active visual pathway glioma

- History of malignant peripheral nerve sheath tumor or ther cancer other than
surgically cured non-melanoma skin cancer or cervical carcinoma in situ

- Ongoing radiation therapy, chemotherapy, hormonal therapy directed at the tumor, or
immunotherapy.

- Inability to return for follow-up visits or obtain follow-up studies

- Severe cardiovascular disease

- Pre-existing sever psychiatric condition or history of psychiatric disorder requiring
hospitalization or a history of suicidal ideation or attempt.

- Thyroid dysfunction not responsive to therapy.

- Uncontrolled diabetes mellitus

- History of seropositivity for HIV

- Subjects who are pregnant, lactating, or of reproductive potential and not practicing
an effective means of contraception.

- Any medical condition requiring chronic systemic corticosteroids.

- Subjects who are known to be actively abusing alcohol or drugs.
We found this trial at
1
site
4401 Penn Avenue
Pittsburgh, Pennsylvania 15224
412-692-5325
Children's Hospital of Pittsburgh of UPMC UPMC is one of the leading nonprofit health systems...
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Pittsburgh, PA
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