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The Conundrum of Rash Management of EGFR Inhibit The Conundrum of Rash Management of EGFR Inhibit
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EGFR Inhibit EGFR Inhibit




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Treatment Algorithm for Dermatological
Reactions Associated with EGFR Inhibitors

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Release date: October 9, 2006
Available for credit through: (Accreditation Expired)

Program Description

New therapies targeting the epidermal growth factor receptor (EGFR) have been used in the treatment of a variety of cancers. Although generally well tolerated, EGFR inhibitors are associated with the development of dermatologic reactions (e.g., papulopustular rash, xerosis, pruritus, periungual inflammation, and alopecia) in most patients. At present, little is known about the etiology of these reactions, and no evidence-based management guidelines have been set forth in the dermatologic literature. Early recognition of and attention to any new skin reaction is important, as is distinguishing between typical rash presentation, secondary infection, and steroid-induced acne. Of interest, data from clinical studies have shown a positive correlation between the development of rash and response and/or survival, thus suggesting that rash may be a surrogate marker of efficacy. The possibility that EGFR inhibitor-related rash is associated with success of treatment offers the potential to titrate the dosing of chemotherapeutic agents on a case-by-case basis. Lack of rash may signal the need for alternative therapy (if available) or an increase in dose (if maximum-tolerated dose is not being used), whereas the presence of rash may allow dose reduction.

Target Audience

This activity is intended for oncologists, pharmacists, nurses, and other clinicians caring for patients with cancer.

Educational Objectives

Upon completion of this educational activity participants will be able to:

  • Understand the dual role of the rash associated with EGFR inhibitor treatment as a side-effect and as clinical surrogate marker for clinical activity
  • Recognize when to implement early treatment to manage these adverse skin reactions
  • Titrate the dosages of various components of chemotherapeutic combinations to achieve best patient outcome

Disclaimer

©2006 ArcMesa Educators / CMEdiscovery.com. All rights reserved. None of the contents may be reproduced in any form without prior written permission from ArcMesa Educators.

The views and opinions expressed in this activity are those of the faculty. They do not reflect the views of Genentech, Inc., OSI Pharmaceuticals, any other manufacturer of pharmaceuticals, or ArcMesa Educators.

The recommendations made in this program are based upon a combination of randomized clinical trials, current guidelines, and the clinical practice experience of the participating panelists. Any medications, diagnostic procedures or treatments discussed by the panelists should not be utilized without evaluation of their patient's conditions. Participants are urged to consult the full prescribing information on any drug mentioned in this activity for recommended dosage, indications, contraindications, warnings, precautions, and adverse effects before prescribing any medication.





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Faculty

Roy S. Herbst, MD, PhD
Roy S. Herbst, MD, PhD
Professor
Chief, Section of Thoracic Medical Oncology
Co-Chairman, Phase I Working Group
Dept. of Thoracic/Head and Neck Medical Oncology
Dept. of Cancer Biology
The University of Texas
M. D. Anderson Cancer Center
Houston, TX

Mario Lacouture, MD
Mario Lacouture, MD
Director, SERIES Clinic
Assistant Professor
Department of Dermatology
Robert H. Lurie Comprehensive Cancer Center
Northwestern University, Chicago, IL

Roman Perez-Soler, MD
Roman Perez-Soler, MD
Gutman Professor of Medicine
Chairman, Department of Oncology
Montefiore Medical Center
Albert Einstein College of Medicine
NYU Medical Center
Bronx, NY

Sandy Kurtin, RN, MS, AOCN, NP
Sandy Kurtin, RN, MS, AOCN®, NP
Nurse Practitioner
Hematology/Oncology
Arizona Cancer Center
Tucson, AZ