Immune checkpoint inhibitor-related dermatologic adverse events.
Immune checkpoint inhibitor-related dermatologic adverse events.
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DOI:
10.1016/j.jaad.2020.03.132
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发表时间:
2020-11
影响因子:
13.8
通讯作者:
Lacouture ME
中科院分区:
文献类型:
--
作者:
Geisler AN;Phillips GS;Barrios DM;Wu J;Leung DYM;Moy AP;Kern JA;Lacouture ME
Immune checkpoint inhibitors have emerged as a pillar in the management of advanced malignancies. However, nonspecific immune activation may lead to immune-related adverse events, wherein the skin and its appendages are the most frequent targets. Cutaneous immune-related adverse events include a diverse group of inflammatory reactions, with maculopapular rash, pruritus, psoriasiform and lichenoid eruptions being the most prevalent subtypes. Cutaneous immune-related adverse events occur early, with maculopapular rash presenting within the first 6 weeks after the initial immune checkpoint inhibitor dose. Management involves the use of topical corticosteroids for mild to moderate (grades 1–2) rash, addition of systemic corticosteroids for severe (grade 3) rash, and discontinuation of immunotherapy with grade 4 rash. Bullous pemphigoid eruptions, vitiligo-like skin hypopigmentation/depigmentation, and psoriasiform rash are more often attributed to programmed cell death-1/programmed cell death ligand-1 inhibitors. The treatment of bullous pemphigoid eruptions is similar to the treatment of maculopapular rash and lichenoid eruptions, with the addition of rituximab in grade 3–4 rash. Skin hypopigmentation/depigmentation does not require specific dermatologic treatment aside from photoprotective measures. In addition to topical corticosteroids, psoriasiform rash may be managed with vitamin D3 analogues, narrowband ultraviolet B light phototherapy, retinoids, or immunomodulatory biologic agents. StevenseJohnson syndrome and other severe cutaneous immune-related adverse events, although rare, have also been associated with checkpoint blockade and require inpatient care as well as urgent dermatology consultation.
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DOI:
10.1016/s1470-2045(16)30053-5
发表时间:
2016-07
期刊:
The Lancet. Oncology
影响因子:
--
作者:
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通讯作者:
Kluger HM
影响因子:
6.2
作者:
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通讯作者:
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影响因子:
50.5
作者:
Champiat, S.;Lambotte, O.;Marabelle, A.
通讯作者:
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影响因子:
51.1
作者:
Antonia, Scott J.;Lopez-Martin, Jose A.;Calvo, Emiliano
通讯作者:
Calvo, Emiliano
影响因子:
7.2
作者:
Ali, Omar Hasan;Diem, Stefan;Flatz, Lukas
通讯作者:
Flatz, Lukas