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Cutaneous Adverse Events of Systemic Melanoma Treatments

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Melanoma

Abstract

Cutaneous adverse events (AEs) are frequent with systemic melanoma treatments. As a result of a paradigmatic shift in melanoma management from traditional cytotoxic chemotherapy to immunotherapies and targeted therapies as first-line treatment, the spectrum of skin AEs to these treatments has significantly broadened. Cutaneous toxicities from anticancer therapy manifest as doubly burdensome as visible stigmatization often carries profound psychosocial implications. Early detection and treatment help to minimize a reduction in patients’ quality of life and maximize anticancer treatment adherence and outcome. The knowledge of typical presentations associated with the specific drug regimen administered to the patient is essential for timely management of these conditions. A dermatological evaluation of the skin condition appears to be essential for an interdisciplinary approach as very often even dramatic skin presentations do not necessitate a cessation of the potentially lifesaving antineoplastic drug. Since the onset of AEs of some therapies can take up to several months or years and may also occur in cancer survivors long after completion of their therapy, thorough dermatological follow-up may be advised even after successful completion of antineoplastic treatments.

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Abbreviations

AD:

Atopic dermatitis

ADLs:

Activities of daily living

AE:

Adverse event

AH:

Antihistamines

AK:

Actinic keratosis

BP:

Bullous pemphigoid

BPAG:

Bullous pemphigoid antigen

BRAF wt:

BRAF wild-type mutation

BRAFi:

BRAF inhibitor

BSA:

Body surface area

CIA:

Chemotherapy-induced alopecia

CsA:

Cyclosporin A

CTCAE:

Common Terminology Criteria for Adverse Events

CTLA-4:

Cytotoxic T-lymphocyte antigen-4

cuSCC/SCC:

(Cutaneous) Squamous cell carcinoma

DEJ:

Dermo-epidermal junction

DRESS:

Drug reaction with eosinophilia and systemic symptoms

DTIC:

5-(3,3-Dimethyl-1-triazeno) imidazole-4-carboxamide

EGFRi:

Epidermal growth factor receptor inhibitor

FDA:

Food and Drug Administration

H&E:

Hematoxylin and Eosin stain

HDAC:

Histone deacetylase

HFS:

Hand-foot syndrome

ICI:

Immune checkpoint inhibitor

IDO:

Indoleamine-pyrrole 2,3-dioxygenase

ircAE:

Immune-related cutaneous adverse event

irAE:

Immune-related adverse event

KA:

Keratoacanthoma

LP:

Lichen planus

MAPK pathway:

Mitogen-activated protein kinase pathway

MEKi:

MEK inhibitor

MMF:

Mycophenolate mofetil

MTIC:

5-3-Methyltriazen-1-yl-imidazo-4-carboxamide

MTX:

Methotrexate

NSCLC:

Non-small cell lung cancer

OS:

Overall survival

OTC:

Over-the-counter

PD-1:

Programmed cell death protein-1

PD-L1:

Programmed cell death ligand-1

PFS:

Progression-free survival

QoL:

Quality of life

RCC:

Renal cell carcinoma

RR:

Response rate

SCAR:

Severe cutaneous adverse reaction

SJS:

Stevens-Johnson syndrome

TCR:

T-cell receptor

TEN:

Toxic epidermolytic necrolysis

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Correspondence to Mario E. Lacouture .

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© 2019 Springer Science+Business Media, LLC, part of Springer Nature

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Menzer, C., Chen, S.T., Phillips, G.S., Lacouture, M.E. (2019). Cutaneous Adverse Events of Systemic Melanoma Treatments. In: Fisher, D., Bastian, B. (eds) Melanoma. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-7147-9_38

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  • DOI: https://doi.org/10.1007/978-1-4614-7147-9_38

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  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4614-7148-6

  • Online ISBN: 978-1-4614-7147-9

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