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Can J Urol ; 30(3): 11558-11561, 2023 06.
Article in English | MEDLINE | ID: mdl-37344468

ABSTRACT

Fumarate hydratase deficient (FHdef) renal cell carcinoma (RCC) is rare, highly aggressive and is believed to arise mostly in the setting of hereditary leiomyomatosis RCC (HLRCC) syndrome with a germline mutation of fumarate hydratase (FH) gene. There is currently little evidence regarding the most effective systemic treatment for advanced FHdef RCC. We present three cases of metastatic FHdef RCC, all achieving tumor response with combination immunotherapy ipilimumab and nivolumab (Ipi/Nivo). A 50-year-old male, a 27-year-old male and a 48-year-old female. The clinical features, diagnosis and medical imaging are reviewed.


Subject(s)
Carcinoma, Renal Cell , Kidney Neoplasms , Skin Neoplasms , Male , Female , Humans , Middle Aged , Adult , Carcinoma, Renal Cell/drug therapy , Carcinoma, Renal Cell/genetics , Carcinoma, Renal Cell/pathology , Kidney Neoplasms/drug therapy , Kidney Neoplasms/genetics , Kidney Neoplasms/pathology , Fumarate Hydratase/genetics , Immune Checkpoint Inhibitors , Germ-Line Mutation , Skin Neoplasms/drug therapy , Skin Neoplasms/genetics
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