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临床试验/NCT00121511
NCT00121511已完成不适用

The Effect of Efudex (5-fluorouracil) Treatment on Photoaged Skin

University of Michigan2 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2005年7月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
21
试验地点
2
主要终点
Actinic Keratoses resolution and improvement in photoaging

研究概览

简要总结

The researchers propose that skin improvements may be seen following a course of Efudex, (5-fluorouracil), a FDA-approved topical therapy (applied directly to the skin). These improvements could be the result of both a reduction of actinic keratoses (small red horny growths or flesh-colored wartlike growths caused by overexposure to ultraviolet radiation or the sun) and improvement of sun-damaged skin.

In addition, this research study is being done to determine if the expression of p53, a tumor suppressor gene (its activity stops the formation of tumors), is decreased following Efudex treatment. Mutations (abnormal changes) in the gene, called p53, are associated with a certain type of skin cancer. In addition, p53-mutated genes are known to exist in non-cancerous sun-damaged skin. Thus, the presence of p53 mutations may serve as a marker for both sun damage and an elevated risk of developing skin cancer.

详细描述

Efudex (5-fluorouracil) has been used as topical chemotherapy for the treatment of actinic keratoses (AKs) since the 1950's. Through many years of use, Efudex has been deemed to be a safe and effective therapy. It requires, however, a high level of patient compliance and is known to cause a vigorous inflammatory reaction when actinic keratoses are treated. It has the distinct advantage of identifying precancerous skin lesions not apparent on clinical inspection or palpation. Following a course of Efudex to the face, patients have been noted to have fewer signs of dermatoheliosis.

The investigators propose to determine if Efudex is associated with improvement of aging skin in the setting of treating actinic keratoses. The researchers hope to demonstrate less p53 staining following Efudex treatment. It is proposed that the skin improvements seen following a course of Efudex are due to both reduction of actinic keratoses and impact on photoaging. The researchers propose to quantify the effects of Efudex therapy on the immunohistochemical staining properties of facial skin with respect to p53 and procollagen. The hypothesis is that Efudex therapy will decrease p53 immunostaining thus providing biochemical evidence to support this treatment in the reduction of actinic keratoses with concomitant improvement of aging skin.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 50 or older of either gender.
  • Patients must have actinic keratoses
  • Patients must have clinical photoaging judged by rhytides, dyspigmentation, poikiloderma, lentigines, skin thinning, and/or telangiectases.
  • Subjects must be in generally good health and willing to undergo skin biopsies from the face.
  • Subjects must be willing and able to comply with the requirements of the protocol.
  • You must live within a reasonable driving distance of Ann Arbor, Michigan, and/or be able to attend all of the scheduled appointments during the study.

排除标准

  • Oral retinoid therapy (such as Accutane) within two months of study entry.
  • Topical retinoid, imiquimod, or diclofenac therapy within 2 months of study entry.
  • Prior laser re-surfacing, chemical peels for actinic keratoses or aging skin.
  • Pregnant or nursing subjects.
  • Non-compliant subjects.
  • Subjects with a significant medical history or concurrent illness that the investigator feels is not safe for study participation.
  • Prior systemic treatment with 5-fluorouracil.
  • Known history of allergy to lidocaine (numbing medication), 5-fluoruracil, or any other known components of Efudex.

结局指标

主要结局

Actinic Keratoses resolution and improvement in photoaging

次要结局

  • Changes in p53 immunostaining intensity will be used to assess response
  • Collagen production will be evaluated by Western blotting, immunohistology, and RT-PCR

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dana L. Sachs, MD

Professor of Dermatology, Medical School

University of Michigan

研究点 (2)

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