Celecoxib in Preventing Basal Cell Carcinoma in Patients With Basal Cell Nevus Syndrome

June 25, 2013 updated by: University of California, San Francisco

A Phase II Randomized, Double-Blind, Placebo-Controlled Clinical Trial of Celecoxib in Subjects With Basal Cell Nevus Syndrome

RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development of cancer. The use of celecoxib may be an effective way to prevent the development of basal cell carcinoma.

PURPOSE: Randomized phase II trial to determine the effectiveness of celecoxib in preventing basal cell carcinoma in patients who have basal cell nevus syndrome.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

OBJECTIVES:

  • Determine whether celecoxib prevents the development of basal cell carcinoma in patients with basal cell nevus syndrome.

OUTLINE: This is a randomized, double-blind, placebo-controlled, multicenter study. Patients are randomized to 1 of 2 arms.

  • Arm I: Patients receive oral celecoxib twice daily.
  • Arm II: Patients receive oral placebo twice daily. Treatment continues for 2 years in the absence of unacceptable toxicity.

Patients are followed every 3 months for 3 years.

PROJECTED ACCRUAL: A total of 60 patients (30 per arm) will be accrued for this study.

Study Type

Interventional

Enrollment (Anticipated)

60

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • California
      • San Francisco, California, United States, 94115
        • UCSF Comprehensive Cancer Center
    • New York
      • New York, New York, United States, 10032
        • Herbert Irving Comprehensive Cancer Center at Columbia University Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

DISEASE CHARACTERISTICS:

  • Histologically confirmed basal cell carcinoma (BCC)

    • At least 5 prior BCCs AND
    • At least 4 BCCs within the past year

  • Meets diagnostic criteria for basal cell nevus syndrome (BCNS)

    • Any 1 of the following:

      • More than 2 BCCs or 1 before age 20
      • Histologically confirmed odontogenic keratocysts of the jaw
      • 3 or more palmar and/or plantar pits
      • Bilamellar calcification of the falx cerebri (if less than 20 years of age)
      • Fused, bifid, or markedly splayed ribs
      • First degree relative with BCNS
      • PTC gene mutation in normal tissue OR

    • Any 2 of the following:

      • Macrocephaly determined after adjustment for height
      • Congenital malformations (e.g., cleft lip or palate, frontal bossing, "coarse face", or moderate or severe hypertelorism)
      • Skeletal abnormalities (e.g., Sprengel deformity, marked pectus deformity, or marked syndactyly of the digits)
      • Radiological abnormalities (e.g., bridging of the sella turcica, vertebral anomalies, modeling defects of the hands and feet, or flame-shaped lucencies of the hands or feet)
      • Ovarian fibroma
      • Medulloblastoma

PATIENT CHARACTERISTICS:

Age:

  • 18 to 75

Performance status:

  • Not specified

Life expectancy:

  • Not specified

Hematopoietic:

  • WBC greater than 3,000/mm^3
  • Platelet count greater than 125,000/mm^3
  • Hemoglobin greater than 12.0 g/dL (women)
  • Hemoglobin greater than 13.0 g/dL (men)
  • No significant coagulation defect

Hepatic:

  • Bilirubin normal
  • ALT/AST no greater than 1.5 times upper limit of normal (ULN)
  • No chronic or acute hepatic disorder

Renal:

  • Creatinine no greater than 1.5 times ULN
  • BUN normal
  • Electrolytes within normal
  • No chronic or acute renal disorder

Cardiovascular:

  • No congestive heart failure

Gastrointestinal:

  • No active gastrointestinal disease
  • No inflammatory bowel disease
  • No chronic or acute pancreatic disorder
  • No history of gastrointestinal ulceration allowed except with permission of primary care physician
  • No esophageal, gastric, pyloric channel, or duodenal ulceration within the past 30 days
  • Stool hematest normal

Other:

  • No prior invasive malignancy within the past 5 years except nonmelanoma skin cancer, stage I cervical cancer, stage 0 chronic lymphoblastic leukemia, or medulloblastoma
  • No hypersensitivity to COX-2 inhibitors, nonsteroidal anti-inflammatory drugs (NSAIDs), salicylates, or sulfonamides
  • No other condition that would preclude study involvement
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Not specified

Chemotherapy:

  • At least 2 weeks since prior topical agents as chemoprevention
  • At least 1 year since other prior chemotherapy

Endocrine therapy:

  • At least 1 month since prior oral or IV corticosteroids
  • At least 6 months since prior inhaled corticosteroid use for longer than 4 weeks
  • At least 2 weeks since prior topical glucocorticoids
  • No concurrent topical glucocorticoids
  • Concurrent oral and IV corticosteroid use of less than 2 weeks within 6 months allowed
  • Concurrent inhaled corticosteroid use of less than 4 weeks within 6 months allowed

Radiotherapy:

  • Not specified

Surgery:

  • Not specified

Other:

  • At least 2 weeks since prior topical retinoids or alpha-hydroxy acids (e.g., glycolic acid or lactic acid)
  • At least 2 weeks since prior topical medications
  • At least 30 days since prior investigational agents
  • At least 2 months since prior NSAIDs given more than 3 times/week
  • At least 2 months since prior aspirin dose of more than 100 mg/day given more than 3 times/week
  • At least 6 months since prior oral retinoids
  • No concurrent chronic NSAIDs (more than 3 times per week for at least 2 weeks)
  • No concurrent aspirin dose of more than 100 mg/day
  • No concurrent topical medications
  • No concurrent fluconazole
  • No concurrent lithium
  • No concurrent retinoids (including topical administration) or alpha-hydroxy acids
  • No other concurrent investigational agents

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Masking: Double

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Prevention of the development of basal cell carcinoma

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of California, San Francisco

Collaborators

National Cancer Institute (NCI)

Investigators

  • Study Chair: Ervin Epstein, MD, University of California, San Francisco

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

February 1, 2001

Study Completion (Actual)

July 1, 2007

Study Registration Dates

First Submitted

September 13, 2001

First Submitted That Met QC Criteria

January 26, 2003

First Posted (Estimate)

January 27, 2003

Study Record Updates

Last Update Posted (Estimate)

June 26, 2013

Last Update Submitted That Met QC Criteria

June 25, 2013

Last Verified

July 1, 2007

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • UCSF-U19-CA81888-BC
  • CDR0000068817 (Registry Identifier: PDQ (Physician Data Query))
  • UCSF-H473-16531-02B
  • NCI-P01-0190

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Non-melanomatous Skin Cancer

Clinical Trials on celecoxib

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Bangladesh

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

3
Subscribe