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Celecoxib in Preventing Skin Cancer in Patients With Actinic Keratoses

2013년 8월 1일 업데이트: University of Alabama at Birmingham

A Phase II/III Randomized, Double-Blind, Placebo-Controlled Clinical Trial Of Celecoxib In Subjects With Actinic Keratoses

RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. The use of celecoxib may be an effective way to prevent actinic keratoses.

PURPOSE: Randomized phase II/III trial to determine the effectiveness of celecoxib in preventing skin cancer in patients who have actinic keratoses.

연구 개요

상세 설명

OBJECTIVES:

  • Compare celecoxib vs placebo in terms of preventing the development of new actinic keratoses in patients with actinic keratoses.
  • Compare these treatment regimens in terms of inducing regression of actinic keratoses in these patients.
  • Determine the safety of this drug in these patients.
  • Compare the effect of these treatment regimens on potential surrogate end-point biomarkers in areas of actinic keratosis, sun-exposed skin, and non-sun-exposed skin and correlate these biomarkers with clinical outcome in these patients.

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

  • Arm I: Patients receive oral celecoxib twice daily for 9 months in the absence of disease progression or unacceptable toxicity.
  • Arm II: Patients receive oral placebo as in arm I. Patients are followed at 2 months after completing treatment.

PROJECTED ACCRUAL: A total of 240 patients (120 per treatment arm) will be accrued for this study.

연구 유형

중재적

단계

  • 2 단계
  • 3단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Alabama
      • Birmingham, Alabama, 미국, 35294-3300
        • University of Alabama at Birmingham Comprehensive Cancer Center
    • California
      • Irvine, California, 미국, 92697
        • Chao Family Comprehensive Cancer Center at University of California Irvine Cancer Center
    • Michigan
      • Ann Arbor, Michigan, 미국, 48109-0314
        • University Of Michigan Comprehensive Cancer Center
    • Missouri
      • Saint Louis, Missouri, 미국, 63110
        • Siteman Cancer Center at Barnes-Jewish Hospital
    • New York
      • Rochester, New York, 미국, 14642
        • James P. Wilmot Cancer Center at University of Rochester Medical Center
    • Texas
      • Houston, Texas, 미국, 77030-4009
        • University of Texas - MD Anderson Cancer Center
    • Wisconsin
      • Madison, Wisconsin, 미국, 53792-6164
        • University of Wisconsin Comprehensive Cancer Center

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

DISEASE CHARACTERISTICS:

  • Diagnosis of Fitzpatrick skin types I, II, or III
  • Sun-damaged skin with 10-40 actinic keratoses on the upper extremities (upper arms, forearms, and hands), neck, face, and scalp combined

PATIENT CHARACTERISTICS:

Age:

  • 18 and over

Performance status:

  • Not specified

Life expectancy:

  • Not specified

Hematopoietic:

  • WBC at least 3,000/mm^3
  • Platelet count at least 125,000/mm^3
  • Hemoglobin at least lower limit of normal
  • No significant bleeding disorder

Hepatic:

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

Renal:

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

Gastrointestinal:

  • No history of or active inflammatory bowel disease
  • No active pancreatitis
  • Not diagnosed with esophageal, gastric, pyloric channel, or duodenal ulceration within the past 30 days

Other:

  • No history of keloid formation
  • No known photosensitivity disorder
  • No history of hypersensitivity or adverse reaction to sulfonamides, COX-2 inhibitors, salicylates, or other NSAIDs
  • No other condition that would preclude study
  • No other medical or psychosocial condition that would preclude study
  • No other malignancy within the past 5 years except:

    • Carcinoma in situ of the cervix
    • Curatively excised nonmelanoma skin cancer
    • Stage 0 chronic lymphocytic leukemia
    • Any cancer for which the patient is currently without evidence of disease, has not been treated for tumor within the past 6 months, has no current or planned therapy, and has an expected disease-free survival of at least 5 years
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • At least 30 days since prior systemic immunotherapy
  • No concurrent immunotherapy

Chemotherapy:

  • At least 3 months since prior topical fluorouracil (5-FU)
  • At least 6 months since other prior topical chemotherapy
  • No concurrent topical chemotherapy, including 5-FU
  • No other concurrent chemotherapy

Endocrine therapy:

  • At least 6 months since prior oral or IV corticosteroids for more than 2 consecutive weeks
  • At least 6 months since prior inhaled or nasal corticosteroids for more than 4 weeks duration
  • At least 14 days since prior topical corticosteroids
  • At least 30 days since prior nasal corticosteroids (except mometasone)
  • No concurrent oral or IV corticosteroids for more than 2 consecutive weeks during any 6 month period during study
  • No concurrent inhaled or nasal steroids (except mometasone) for more than 4 weeks during any 6 month period during study
  • No concurrent hormonal or steroidal therapy, including topical corticosteroids
  • Concurrent hormone replacement therapy (e.g., estrogen or thyroid hormone replacement) allowed

Radiotherapy:

  • At least 6 months since prior local radiotherapy to areas being studied
  • At least 30 days since other prior radiotherapy
  • No concurrent radiotherapy, including local radiotherapy to areas being studied

Surgery:

  • Not specified

Other:

  • At least 30 days since prior cryotherapy to target lesions
  • At least 60 days since prior laser resurfacing, dermabrasion, or chemical peels
  • At least 30 days since prior investigational medication
  • At least 14 days since prior topical alphahydroxyacids (e.g., glycolic acid or lactic acid) or retinoids
  • At least 30 days since prior systemic psoralens or retinoids
  • At least 30 days since prior treatment for esophageal, gastric, pyloric channel, or duodenal ulcers
  • At least 30 days since prior aspirin (more than 100 mg/day), other nonsteroidal anti-inflammatory drugs (NSAIDs) or COX-2 inhibitors at a frequency of at least 3 times per week for more than 2 weeks (except cardioprotective doses of aspirin (no more than 100 mg/day)
  • No concurrent systemic psoralens or retinoids
  • No concurrent prescription or over-the-counter topical medications to areas being studied (e.g., vitamin A derivatives)
  • No concurrent cryotherapy to target lesions
  • No concurrent laser resurfacing, dermabrasion, or chemical peels
  • No other concurrent investigational medications
  • No concurrent fluconazole or lithium
  • No concurrent chronic NSAIDs or COX-2 inhibitors (at least 3 times per week for more than 2 consecutive weeks per year)
  • Concurrent cardioprotective doses of oral aspirin (100 mg per day or less) allowed
  • Concurrent moisturizer/emollient or sunscreen allowed

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 방지
  • 할당: 무작위
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 삼루타

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Group 1 active arm
receipt of active drug
실험적: Group 2 active arm
receipt of active drug
실험적: group 2 placebo arm
receipt of placebo

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
Compare celecoxib vs placebo in terms of preventing the development of new actinic keratoses in patients with actinic keratoses.
기간: baseline to 2 months after last dose
baseline to 2 months after last dose

2차 결과 측정

결과 측정
기간
Compare these treatment regimens in terms of inducing regression of actinic keratoses in these patients.
기간: baseline to 2 months after last dose
baseline to 2 months after last dose
Compare the effect of these treatment regimens on potential surrogate end-point biomarkers in areas of actinic keratosis, sun-exposed skin, and non-sun-exposed skin and correlate these biomarkers with clinical outcome in these patients.
기간: baseline to 2 months after last dose
baseline to 2 months after last dose

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 연구 의자: Craig A. Elmets, MD, University of Alabama at Birmingham

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2001년 12월 1일

기본 완료 (실제)

2005년 12월 1일

연구 완료 (실제)

2005년 12월 1일

연구 등록 날짜

최초 제출

2001년 12월 7일

QC 기준을 충족하는 최초 제출

2003년 1월 26일

처음 게시됨 (추정)

2003년 1월 27일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2013년 8월 5일

QC 기준을 충족하는 마지막 업데이트 제출

2013년 8월 1일

마지막으로 확인됨

2012년 11월 1일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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