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DOI 10.1111/dth.15747

Медицинская библиотека · Dermatologic therapy · 2022

Dermatological adverse events under programmed cell death-1 inhibitors as a prognostic marker in metastatic melanoma.

Shreberk-Hassidim Rony, Aizenbud Lilach, Lussheimer Shalev, Thomaidou Elena, Bdolah-Abram Tali, Merims Sharon, Popovtzer Aron, Maly Alex, Lotem Michal, Zlotogorski Abraham

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Аннотация

Melanoma is widely treated with programmed cell death-1 (PD-1) inhibitors. As part of their anti-tumor immunity effect, they increase the susceptibility to cutaneous immune-related adverse events (cIRAE) among other autoimmune effects. To characterize the manifestations of cIRAE in melanoma patients treated with PD-1 inhibitors, and evaluate the correlation with tumor response. A retrospective study of 95 metastatic malignant melanoma patients treated with PD-1 inhibitors at the Hadassah Medical Center during 2013-2016. The most common cIRAE was pruritus reported by 39 (41%) patients. All other cIRAE were noted in 34 patients (35.8%), of which the most common cutaneous manifestation was vitiligo, demonstrated in 17 patients (17.9%) followed by various rashes (7.4%, including erythema multiforme, oral lichen planus, photosensitive rash, insect bite-like reaction, and urticaria), psoriasiform rash (3.2%), bullous pemphigoid (3.2%), and eczema (1%). Interestingly, higher response rates to immunotherapy were demonstrated in patients who developed pruritus (85%) and cIRAE (88%), with lower mortality rates in the cIRAE group (38.2%) versus the non-cIRAE group (70.5%, p = 0.002). cIRAE are common among malignant melanoma patients treated with PD-1 inhibitors and may be a marker for favorable prognosis.

Для цитирования: Shreberk-Hassidim Rony, Aizenbud Lilach, Lussheimer Shalev, Thomaidou Elena, Bdolah-Abram Tali, Merims Sharon, Popovtzer Aron, Maly Alex, Lotem Michal, Zlotogorski Abraham. Dermatological adverse events under programmed cell death-1 inhibitors as a prognostic marker in metastatic melanoma.. Dermatologic therapy. 2022. DOI: 10.1111/dth.15747.

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