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dc.contributor.authorYılmaz, Mesut
dc.contributor.authorGüven Meşe, Şermin
dc.contributor.authorÇelik, Uğur
dc.date.accessioned2019-12-30T09:15:08Z
dc.date.available2019-12-30T09:15:08Z
dc.date.issued2020en_US
dc.identifier.citationYılmaz, M., Güven Meşe, Ş. ve Çelik, U. (2020). Nivolumab-induced lichen planus. Journal of Oncology Pharmacy Practice, 26(3), 758-760. https://doi.org/10.1177/1078155219866248en_US
dc.identifier.issn1078-1552
dc.identifier.issn1477-092X
dc.identifier.urihttps://doi.org/10.1177/1078155219866248
dc.identifier.urihttps://hdl.handle.net/20.500.12511/4796
dc.description.abstractIntroduction:Renal cell carcinomas account for 90% of all malignant neoplasms of the kidney. The most common types of renal cancer in adults are clear cell and papillary renal cell carcinoma; sporadic cases of renal carcinomas containing chromosomal translocations are rare, more usually occurring in children and young adults. Nivolumab (a fully human immunoglobulin G4 PD-1 checkpoint inhibitor antibody) has received the Food and Drug Administration approval for the treatment of metastatic renal cell carcinoma in patients who have received prior antiangiogenic therapy. Skin reactions are the most common side-effects under treatment with anti-PD-1 antibodies and play an important role for patients. Case report:We report a nivolumab-induced lichen planus as an immune-related adverse event in a young woman who was treated for advanced renal cell carcinoma. After the ninth dose of nivolumab treatment, she was consulted to the dermatologist because of skin lesions, and lichen planus was diagnosed.Management and outcome She was treated with topical corticosteroids and clobetasol propionate cream. Her lesions regressed after the local therapy within one month, allowing for uninterrupted nivolumab therapy. Discussion:Skin adverse events are the most common side-effects under immunotherapy and play an important role for patients and usually develop early in the course of treatment. The most frequent skin reactions are rash, pruritus, and vitiligo. Serious skin adverse events are rare and do not usually require dose reductions or treatment discontinuation. We report a nivolumab-induced lichen planus after the ninth dose of nivolumab.en_US
dc.language.isoengen_US
dc.publisherSAGE Publicationsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectImmune-Related Adverse Eventen_US
dc.subjectImmunotherapyen_US
dc.subjectLichen Planusen_US
dc.subjectNivolumaben_US
dc.titleNivolumab-induced lichen planusen_US
dc.typearticleen_US
dc.relation.ispartofJournal of Oncology Pharmacy Practiceen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Deri ve Zührevi Hastalıklar Ana Bilim Dalıen_US
dc.authorid0000-0003-0338-8111en_US
dc.identifier.volume26en_US
dc.identifier.issue3en_US
dc.identifier.startpage758en_US
dc.identifier.endpage760en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1177/1078155219866248en_US
dc.identifier.wosqualityQ4en_US
dc.identifier.scopusqualityQ3en_US


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