Literature DB >> 21537180

Prophylaxis and treatment of dermatologic adverse events from epidermal growth factor receptor inhibitors.

Peggy A Wu1, Yevgeniy Balagula, Mario E Lacouture, Milan J Anadkat.   

Abstract

PURPOSE OF REVIEW: As the number and uses for targeted therapies such as epidermal growth factor receptor inhibitors (EGFRIs) increase, so does the need to recognize and treat the dermatologic side-effects of these agents. Although agents such as gefitinib, erlotinib, cetuximab, lapatinib, and panitumumab have less systemic side-effects than traditional cytotoxic chemotherapy, dermatologic adverse events from EGFRIs are significantly more common. These dermatologic toxicities have previously led to reduction or cessation of therapy and recently have been shown to decrease patients' quality of life. RECENT
FINDINGS: This review provides a symptom-based treatment approach to the common dermatologic adverse effects seen with the epidermal growth factor receptor antagonists: papulopustular rash, xerosis, pruritus as well as hair, nail, and mucosal changes. Each dermatologic toxicity is described; prophylaxis and treatment options, from topical to systemic, are presented based on a review of the current literature with emphasis on new clinical trials results. We also provide specific recommendations based on our practice in a specialty clinic.
SUMMARY: Although the field continues to evolve, this review presents the most up-to-date information on managing dermatologic adverse effects of EGFRIs. Practitioners should find this article to be a practical resource in approaching patients on EGFRIs with dermatologic toxicities. As we learn how to optimally manage the adverse effects of these agents, we practitioners have the opportunity to increase patients' quality of life and decrease reductions or cessations of life-prolonging therapy.

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Year:  2011        PMID: 21537180     DOI: 10.1097/CCO.0b013e3283474063

Source DB:  PubMed          Journal:  Curr Opin Oncol        ISSN: 1040-8746            Impact factor:   3.645


  7 in total

1.  A review of cutaneous toxicities from targeted therapies in the treatment of colorectal cancers.

Authors:  Christopher Urban; Milan J Anadkat
Journal:  J Gastrointest Oncol       Date:  2013-09

2.  Dermatomyositis and chest radiography leading to the diagnosis of lung cancer and subsequent confusions in staging due to the presence of tuberculosis.

Authors:  Swaroop Revannasiddaiah; Manoj Kumar Gupta; Madhup Rastogi; Avinash Arjun Rao Kesari; Rajeev Kumar Seam; Manish Gupta; Suneel Chauhan; Irappa Madabhavi
Journal:  BMJ Case Rep       Date:  2012-04-02

Review 3.  Overview and management of dermatologic events associated with targeted therapies for medullary thyroid cancer.

Authors:  Mario E Lacouture; Kathryn Ciccolini; Richard T Kloos; Mark Agulnik
Journal:  Thyroid       Date:  2014-07-15       Impact factor: 6.568

4.  EGFR inhibitor-induced skin reactions: differentiating acneiform rash from superimposed bacterial infections.

Authors:  Rachel L Braden; Milan J Anadkat
Journal:  Support Care Cancer       Date:  2016-04-27       Impact factor: 3.603

Review 5.  Osimertinib: A Novel Dermatologic Adverse Event Profile in Patients with Lung Cancer.

Authors:  Chia-Yu Chu; Jennifer Choi; Beth Eaby-Sandy; Corey J Langer; Mario E Lacouture
Journal:  Oncologist       Date:  2018-04-12

6.  A review of the treatment options for skin rash induced by EGFR-targeted therapies: Evidence from randomized clinical trials and a meta-analysis.

Authors:  Janja Ocvirk; Steffen Heeger; Philip McCloud; Ralf-Dieter Hofheinz
Journal:  Radiol Oncol       Date:  2013-05-21       Impact factor: 2.991

7.  IL-36γ drives skin toxicity induced by EGFR/MEK inhibition and commensal Cutibacterium acnes.

Authors:  Takashi K Satoh; Mark Mellett; Barbara Meier-Schiesser; Gabriele Fenini; Atsushi Otsuka; Hans-Dietmar Beer; Tamara Rordorf; Julia-Tatjana Maul; Jürg Hafner; Alexander A Navarini; Emmanuel Contassot; Lars E French
Journal:  J Clin Invest       Date:  2020-03-02       Impact factor: 14.808

  7 in total

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