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Review
. 2012 Feb;109(8):133-40.
doi: 10.3238/arztebl.2012.0133. Epub 2012 Feb 24.

Cutaneous side effects of new antitumor drugs: clinical features and management

Affiliations
Review

Cutaneous side effects of new antitumor drugs: clinical features and management

Ralf Gutzmer et al. Dtsch Arztebl Int. 2012 Feb.

Abstract

Background: Many new antitumor drugs have been approved in recent years. Their side-effect profiles are distinct from those of older drugs, and their adverse effects are sometimes highly specific, particularly with respect to the skin.

Methods: This article is based on articles retrieved by a selective search in Medline and the database of the American Society of Clinical Oncology (ASCO), as well as on the authors' personal experience.

Results: Cutaneous adverse effects are among the more common adverse effects of new antitumor drugs: they occur in up to 34% of patients receiving multikinase inhibitors, up to 90% of those receiving selective tyrosine kinase inhibitors (such as EGFR or mutant BRAF inhibitors), and up to 68% of those receiving immunotherapeutic agents (such as CTLA4 inhibitors). These adverse effects can be correlated with therapeutic benefit, but they can also be treatment-limiting because of their severity or visibility.

Conclusion: The recognition and proper management of cutaneous adverse effects is an important part of treatment with new antitumor drugs.

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Figures

Figure 1
Figure 1
Intensity and time-course of the most common cutaneous adverse events during EGFR inhibition
Figure 2
Figure 2
Papulopustular rash during treatment with the EGFR-inhibitor cetuximab
Figure 3
Figure 3
Paronychia with granulation tissue during treatment with the EGFR-inhibitor cetuximab
Figure 4
Figure 4
Maculo-papular rash during treatment with the multikinase inhibitor sorafenib
Figure 5
Figure 5
Hand-foot syndrome during treatment with the multikinase inhibitor sorafenib
Figure 6
Figure 6
Hand-foot syndrome (palmar-plantar erythrodysesthesia) during treatment with pegylated liposome-encapsulated doxorubicin
Figure 7
Figure 7
Papular urticarial rash during treatment with the anti-CTLA-4-antibody ipilimumab

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References

    1. Salomon DS, Brandt R, Ciardiello F, Normanno N. Epidermal growth factor-related peptides and their receptors in human malignancies. Crit Rev Oncol Hematol. 1995;19:183–232. - PubMed
    1. Potthoff K, Hofheinz R, Hassel JC, et al. Interdisciplinary management of EGFR-inhibitor-induced skin reactions: a German expert opinion. Ann Oncol. 2011;22:524–535. - PubMed
    1. Wollenberg A, Kroth J, Hauschild A, Dirschka T. Hautreaktionen unter EGFR-Inhibitoren - Klinik und Management. Dtsch Med Wochenschr. 2010;135:149–154. - PubMed
    1. Gutzmer R, Becker JC, Enk A, et al. Management kutaner Nebenwirkungen von FGFR-Inhibitoren: Empfehlungen eines deutschen Expertengremiums für den primär behandelnden Arzt. J Dtsch Dermatol Ges. 2011;9:195–203. - PubMed
    1. Wollenberg A, Moosmann N, Klein E, Katzer K. A tool for scoring of acneiform skin eruptions induced by EGF receptor inhibition. Exp Dermatol. 2008;17:790–792. - PubMed

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