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Erschienen in: Current Treatment Options in Oncology 11/2016

01.11.2016 | Skin Cancer (BY Kwong, Section Editor)

Cutaneous Complications of Targeted Melanoma Therapy

verfasst von: Emily de Golian, MD, Bernice Y. Kwong, MD, Susan M. Swetter, MD, Silvina B. Pugliese, MD

Erschienen in: Current Treatment Options in Oncology | Ausgabe 11/2016

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Opinion statement

The landscape of advanced and metastatic melanoma therapy has shifted dramatically in recent years. Since 2011, eight drugs (ipilimumab, vemurafenib, dabrafenib, trametinib, cometinib, pembrolizumab, nivolumab, and talimogene laherparepvec) have received FDA approval for the treatment of advanced or metastatic melanoma, including combination regimens of both small molecule kinase and immune checkpoint inhibitors. These therapies have revolutionized the management of unresectable regional nodal and distant melanoma, providing hope of extended survival to patients. As the use of novel agents has increased, so have the cutaneous toxicities associated with these medications. While most skin reactions are low-grade and can be managed conservatively with topical therapies, malignant lesions and more serious or life-threatening drug reactions can arise during therapy, requiring prompt dermatologic recognition and treatment in order to improve patient outcome. Given the survival benefit attributed to these new agents, treating skin toxicity and maintaining patient quality of life is of paramount importance. Oncologists should be aware of the common cutaneous toxicities associated with these medications and should be encouraged to involve dermatologists in the collaborative care of advanced melanoma patients. Close communication between oncologists and dermatologists can help to avoid unnecessary dose reduction or treatment discontinuation and identify situations when treatment cessation is truly warranted.
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Metadaten
Titel
Cutaneous Complications of Targeted Melanoma Therapy
verfasst von
Emily de Golian, MD
Bernice Y. Kwong, MD
Susan M. Swetter, MD
Silvina B. Pugliese, MD
Publikationsdatum
01.11.2016
Verlag
Springer US
Erschienen in
Current Treatment Options in Oncology / Ausgabe 11/2016
Print ISSN: 1527-2729
Elektronische ISSN: 1534-6277
DOI
https://doi.org/10.1007/s11864-016-0434-0

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