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Spots Global Cancer Trial Database for Topical Imiquimod Compared With Surgery in Treating Patients With Basal Cell Skin Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Topical Imiquimod Compared With Surgery in Treating Patients With Basal Cell Skin Cancer

Official Title: A Randomized Controlled Trial of Excisional Surgery Versus Imiquimod 5% Cream for Nodular and Superficial Basal Cell Carcinoma

Study ID: NCT00066872

Study Description

Brief Summary: RATIONALE: Biological therapies such as imiquimod use different ways to stimulate the immune system and stop cancer cells from growing. It is not yet known if topical imiquimod is more effective than surgery in treating basal cell skin cancer. PURPOSE: This randomized phase III trial is studying how well topical imiquimod works compared to surgery in treating patients with basal cell skin cancer.

Detailed Description: OBJECTIVES: * Compare the rate of local recurrence at 3 years in patients with nodular or superficial basal cell skin cancer treated with imiquimod 5% cream vs excisional surgery. * Compare recurrence at 6 months and 1, 2, and 5 years in patients treated with these regimens. * Compare the time to first recurrence in patients treated with these regimens. * Compare the aesthetic appearance of lesion sites in patients treated with these regimens. * Compare pain in patients treated with these regimens. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to participating center and lesion type (nodular vs superficial). Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive topical imiquimod to a single lesion once daily for 6 weeks for a superficial lesion or 12 weeks for a nodular lesion. Patients with early treatment failure or recurrence are offered surgical excision. * Arm II: Patients undergo surgical excision. Patients are followed at 6, 12, and 18 weeks, every 6 months for 1 year, annually for 2 years, and then at 5 years. Peer Reviewed and Funded or Endorsed by Cancer Research UK PROJECTED ACCRUAL: A total of 500 patients will be accrued for this study within 18 months.

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Chesterfield Royal Hospital, Chesterfield, England, United Kingdom

Queen's Medical Centre, Nottingham, England, United Kingdom

Solihull Hospital, Solihull, England, United Kingdom

Contact Details

Name: Mara Ozolins, MS

Affiliation: Queen's Medical Center

Role:

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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