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Neurofibromatosis Type 1Phase 1NCT00053937

Pirfenidone in Treating Young Patients With Neurofibromatosis Type 1 and Plexiform Neurofibromas

A Phase 1 study testing pirfenidone in people with Neurofibromatosis Type 1 and Precancerous Condition, run by National Cancer Institute (NCI) at 15 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. Pirfenidone may slow the growth or prevent further development of plexiform neurofibromas. Read more about this study

Who is it for?
Ages 3 to 21 years
What is being tested?
pirfenidone
How many people
Not given
Where
15 sitesUnited States
Study dates
Dec 2002to not given
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 3 to 21 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

DISEASE CHARACTERISTICS:

  • Diagnosis of neurofibromatosis type 1 (NF1) AND
  • Plexiform neurofibromas
  • Neurofibromas that have grown along the length of a nerve and may involve multiple fascicles and branches (spinal neurofibromas involve 2 or more levels with connection between the levels or extending laterally along the nerve)
  • Potential to cause significant morbidity such as:
  • Head and neck lesions that could compromise airway or great vessels
  • Brachial or lumbar plexus lesions that could cause nerve compression and loss of function
  • Lesions that could result in major deformity (e.g., orbital lesions) or significant cosmetic problems
  • Lesions of the extremity that cause limb hypertrophy or loss of function
  • Painful lesions
  • Meets at least 1 other diagnostic criteria for NF1
  • 6 or more cafe-au-lait spots (at least 0.5 cm in prepubertal patients or at least 1.5 cm in postpubertal patients)
  • Freckling in the axilla or groin
  • Optic glioma
  • 2 or more Lisch nodules
  • Distinctive bony lesion (dysplasia of the sphenoid bone or dysplasia or thinning of long bone cortex)
  • First-degree relative with NF1
  • Measurable plexiform neurofibromas
  • At least 3 cm in 1 dimension
  • Tumor resection not feasible
  • No history of malignant peripheral nerve sheath tumor or other cancer
  • No evidence of an active optic glioma requiring chemotherapy or radiotherapy
  • No malignant glioma

PATIENT CHARACTERISTICS:

Age

  • 3 to 21

Performance status

  • Karnofsky 50-100% (over 10 years of age)
  • Lansky 50-100% (10 years and under)

Life expectancy

  • Not specified

Hematopoietic

  • Absolute granulocyte count at least 1,500/mm^3
  • Hemoglobin at least 9.0 g/dL
  • Platelet count at least 150,000/mm^3

Hepatic

  • Bilirubin normal
  • SGPT no greater than 2 times upper limit of normal
  • No clinically significant hepatic dysfunction that would preclude study participation

Renal

  • Creatinine normal for age OR
  • Creatinine clearance at least 70 mL/min

Cardiovascular

  • No clinically significant cardiac dysfunction that would preclude study participation

Pulmonary

  • No clinically significant pulmonary dysfunction that would preclude study participation

Other

  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for 2 months after study
  • Must be able to take pirfenidone orally
  • No serious infections
  • No clinically significant unrelated systemic illness or organ dysfunction that would preclude study participation

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • At least 30 days since prior immunotherapy
  • No concurrent immunotherapy
  • No concurrent hematopoietic growth factors

Chemotherapy

  • At least 30 days since prior chemotherapy
  • No concurrent chemotherapy directed at the tumor

Endocrine therapy

  • At least 30 days since prior hormonal therapy directed at the tumor
  • No concurrent hormonal therapy directed at the tumor

Radiotherapy

  • At least 90 days since prior radiotherapy to the site of the plexiform neurofibroma
  • No concurrent radiotherapy directed at the tumor

Surgery

  • Not specified

Other

  • Recovered from prior therapy
  • More than 30 days since prior investigational agents
  • No prior pirfenidone
  • No other concurrent investigational agents

Trial locations and contacts

15 sites in 1 country.

15 sites in 1 country

United States15 sites
  • Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

    Baltimore, Maryland, 21231

  • Warren Grant Magnuson Clinical Center - NCI Clinical Studies Support

    Bethesda, Maryland, 20892

  • University of Alabama at Birmingham Comprehensive Cancer Center

    Birmingham, Alabama, 35294-3300

  • Dana-Farber/Harvard Cancer Center at Dana Farber Cancer Institute

    Boston, Massachusetts, 02115

  • Children's Memorial Hospital - Chicago

    Chicago, Illinois, 60614

  • Cleveland Clinic Taussig Cancer Center

    Cleveland, Ohio, 44195

  • Texas Children's Cancer Center

    Houston, Texas, 77030-2399

  • Beth Israel Medical Center - Singer Division

    New York, New York, 10128

  • Children's Hospital of Philadelphia

    Philadelphia, Pennsylvania, 19104

  • Children's Hospital of Pittsburgh

    Pittsburgh, Pennsylvania, 15213

  • Cancer Institute at Oregon Health and Science University

    Portland, Oregon, 97239-3098

  • Mayo Clinic Cancer Center

    Rochester, Minnesota, 55905

  • Washington University School of Medicine

    St Louis, Missouri, 63110

  • University Hospital at State University of New York - Upstate Medical University

    Syracuse, New York, 13210

  • Children's National Medical Center

    Washington D.C., District of Columbia, 20010-2970

Other trials in United States

About this study

Official title: Phase I Trial Of Pirfenidone In Children With Neurofibromatosis Type 1 And Plexiform Neurofibromas

RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. Pirfenidone may slow the growth or prevent further development of plexiform neurofibromas.

PURPOSE: Phase I trial to study the effectiveness of pirfenidone in treating young patients who have neurofibromatosis type 1 and plexiform neurofibroma.

Read the detailed description

OBJECTIVES:

  • Determine the maximum tolerated dose or "comparable dose" of pirfenidone in pediatric patients with neurofibromatosis type 1 and inoperable, symptomatic plexiform neurofibromas.
  • Determine the toxic effects of this drug in these patients.
  • Determine the plasma pharmacokinetics of this drug in these patients.
  • Determine, preliminarily, if this drug could be beneficial for pediatric patients with refractory solid tumors.
  • Assess the quality of life of patients treated with this drug.

OUTLINE: This is an open-label, multicenter, dose-escalation study.

Patients receive oral pirfenidone three times daily on days 1-28. Courses repeat every 28 days for up to 2 years in the absence of disease progression or unacceptable toxicity.

Cohorts of 3-6 patients receive escalating doses of pirfenidone until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

Quality of life is assessed at baseline, before course 4, and then after every 6 courses.

PROJECTED ACCRUAL: A total of 3-18 patients will be accrued for this study within 18 months.

Being tested
pirfenidone
Keywords
plexiform neurofibroma, neurofibromatosis type 1
Medical subject headings
Neurofibromatosis 1, Precancerous Conditions, Neurofibroma, Plexiform

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • pirfenidoneDrug

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Feb 2003 (estimated)
  2. Study startDec 2002

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Prevention
Masking
None (open label)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00053937
Sponsor's protocol ID
CDR0000269598
Other IDs
NCI-03-C-0058A
Status last verified
Apr 2004
First submitted
5 Feb 2003
Last updated
30 Apr 2015
Results posted
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing pirfenidone in people with Neurofibromatosis Type 1 and Precancerous Condition, run by National Cancer Institute (NCI) at 15 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 30 Apr 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 15 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Apr 2015.

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