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Dermatologists' Case Files:                                                                  Use of Immune Response Modifier Therapy in Challenging Patients

A supplement to Skin & Allergy News, supported by an educational grant from 3M Pharmaceuticals and designated by the American Academy of Dermatology (AAD) for AAD continuing medical educational (CME) credit.

 

Topics

  • Introduction
  • Sebaceous Carcinoma in an Elderly Patient
  • Extensive Actinic Keratoses
  • Actinic Keratoses and Warts in a Kidney Transplant Recipient 

Faculty

Hilary E. Baldwin, MD
Associate Professor of Clinical Dermatology
Department of Dermatology
SUNY Downstate Medical Center
Brooklyn, N.Y.

May J. Chow, MD
Director of Dermatology
Wellgroup Health Partners
Chicago Heights, Ill.
Clinical Assistant Professor of Medicine and Dermatology
Midwestern University
Downers Grove, Ill

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Faculty Disclosures

The faculty of this CME activity disclose the following:

Faculty Member
Hilary E. Baldwin, MD Dr. Baldwin has nothing to disclose nor does she discuss the unlabeled use of any drugs.
May J. Chow, MD Dr. Chow has received honoraria from 3M Pharmaceuticals. She discusses the alternatives to approved dosage regimens of imiquimod; the unlabeled use of tazarotene as an adjunct to imiquimod therapy in actinic keratosis; prophylactic maintenance treatment with imiquimod; and the use of imiquimod to treat sebaceous carcinoma or nodular basal cell carcinoma.

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Target Audience

This activity has been developed for dermatologists and other healthcare professionals involved in the diagnosis and treatment of skin conditions for which immune response modifier therapy may be considered.

Educational Needs

The treatment of many commonly encountered skin disorders necessitates elimination of lesions. Such cutaneous disorders include actinic keratoses, external anogenital warts, superficial basal cell carcinomas, squamous cell carcinomas, and common warts. Historically, these lesions have been treated with a variety of surgical and/or chemical lesion-destructive modalities. These therapies have varied in their success rates; in addition, they often produce adverse effects such as pain, swelling, and scarring.

 

Within the past decade, the concept of local immune response modifier (IRM) treatment for many of these diseases has emerged. With IRM therapy, topical application of the medication produces a local upregulation of activity in both the innate and the acquired immune system, yielding proven, safe, antiviral and antitumor activity with limited side effects and ease of application.

 

The results of well-controlled clinical trials form the foundation of any evidence-based approach to medical treatment. In treating individual patients, however, clinicians also receive valuable knowledge from their own experience and that of their colleagues. Using case studies as a basis, this supplement offers the clinical experiences of experts who have used imiquimod in a variety of skin diseases.

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Learning Objectives

By reading and studying this supplement, participants should be able to:

·      Discuss the indications and dosing schedule for the use of imiquimod that are currently approved by the US Food and Drug Administration.

·      Describe the experience of clinicians who treated an elderly patient with sebaceous carcinoma in a case presented in this supplement.

·      Discuss the treatment regimen used for treating a patient with extensive actinic keratoses on the face and upper extremities.

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CME Recognition

This Skin & Allergy News supplement is recognized by the American Academy of Dermatology (AAD) for 1 hour of AAD Category 1 CME credit and may be used toward the American Academy of Dermatology’s Continuing Medical Education Award. This program was developed in accordance with the Accreditation Council for Continuing Medical Education guidelines.

Term of Approval: March 2006—February 28, 2007

Copyright © 2006 Elsevier Inc.

 

 

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