Vehicle-controlled, double-blind, randomized study of imiquimod 5% cream applied 3 days per week in one or two courses of treatment for actinic keratoses on the head

J Am Acad Dermatol. 2007 Aug;57(2):265-8. doi: 10.1016/j.jaad.2007.01.047. Epub 2007 May 18.

Abstract

Background: A shorter dosing regimen of imiquimod for the treatment of actinic keratosis may be effective, with long-term clinical benefits.

Objective: Imiquimod in one or two shorter courses of treatment was evaluated.

Methods: Patients with actinic keratosis lesions on the head applied imiquimod or vehicle cream 3x/wk for 4 weeks (course 1). Patients with remaining lesions received another course of treatment. Complete and partial clearance rates were evaluated after course 1, after course 2 (overall), and 1 year later.

Results: Complete clearance rates were 26.8% (course 1) and 53.7% (overall). Partial clearance rates were 36.6% (course 1) and 61.0% (overall). One-year follow-up recurrence rates were 39% (imiquimod) and 57% (vehicle).

Limitations: Blinded investigators may have been biased toward patients treated with imiquimod identified by treatment site reactions.

Conclusion: Imiquimod 3x/wk in one or two courses of treatment appears to be effective for the treatment of actinic keratoses on the head, providing long-term clinical benefits. Some recurrences do occur, so long-term follow-up is recommended.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aminoquinolines / administration & dosage*
  • Aminoquinolines / adverse effects
  • Aminoquinolines / therapeutic use
  • Double-Blind Method
  • Drug Administration Schedule
  • Facial Dermatoses / drug therapy*
  • Female
  • Humans
  • Imiquimod
  • Keratosis / drug therapy*
  • Male
  • Ointments
  • Photosensitivity Disorders / drug therapy*
  • Recurrence
  • Scalp Dermatoses / drug therapy*
  • Treatment Outcome

Substances

  • Aminoquinolines
  • Ointments
  • Imiquimod