Kuentz Marie Auvray, Blons Hélène, Gimenez-Roqueplo Anne Paule, Just Pierre-Alexandre, Laurent-Puig Pierre, Mejean Arnaud, Oudard Stéphane, Verkarre Virginie
Department of Oncology, European Georges Pompidou Hospital, Assistance publique-hôpitaux de Paris (APHP)-Centre, Université Paris Cité, Paris Cancer Institute CARPEM, Paris, France.
Department of Biochemistry, Molecular Oncology and Pharmacogenetics, European Georges Pompidou Hospital, APHP-Centre, Université Paris Cité, Paris Cancer Institute CARPEM, Paris, France.
Genes Chromosomes Cancer. 2023 Jun;62(6):361-366. doi: 10.1002/gcc.23127. Epub 2023 Feb 13.
Renal cell carcinoma (RCC) with rearrangement of transcription factor for immunoglobulin heavy-chain enhancer 3 (TFE3; TFE3-rearranged RCC) at Xp11.2 is a rare tumor entity but the most frequent among the microphthalmia transcription factor family translocation RCCs. Here, we report the identification of a new VCP::TFE3 fusion gene as the result of a t(X;9)(p11.23;p13.3) translocation identified by whole transcriptome sequencing. No other relevant molecular alteration was identified by whole exome sequencing. This case showed typical morphological features of TFE3-rearranged RCC with positive TFE3 immunostaining and positive TFE3 break-apart fluorescence in situ hybridization. MET was also overexpressed on immunohistochemistry. The patient had metastatic disease and was treated by surgery and five lines of therapy, including 24 months of stable disease on the mesenchymal epithelial transition (MET) inhibitor cabozantinib, with an overall survival of 7 years. In addition to expanding the spectrum of TFE3 rearrangement partners, this report highlights the complexity of these tumors and supports the development of translational programs in renal cancer.
Xp11.2处具有免疫球蛋白重链增强子3转录因子(TFE3;TFE3重排性肾细胞癌)重排的肾细胞癌(RCC)是一种罕见的肿瘤实体,但在小眼畸形转录因子家族易位性肾细胞癌中最为常见。在此,我们报告通过全转录组测序鉴定出一种新的VCP::TFE3融合基因,该基因是由t(X;9)(p11.23;p13.3)易位导致的。全外显子组测序未发现其他相关分子改变。该病例显示出TFE3重排性肾细胞癌的典型形态学特征,TFE3免疫染色阳性,TFE3分离荧光原位杂交阳性。免疫组化还显示MET过表达。该患者有转移性疾病,接受了手术及五种治疗方案,包括在间充质上皮转化(MET)抑制剂卡博替尼治疗下病情稳定24个月,总生存期为7年。除了扩大TFE3重排伙伴的范围外,本报告还强调了这些肿瘤的复杂性,并支持肾癌转化研究项目的开展。