TFE3 Rearrangements in Adult Renal Cell Carcinoma

TFE3型 肾细胞癌 基因重排 医学 病理 生物 增强子 转录因子 基因 遗传学
作者
William R. Sukov,Jennelle C. Hodge,Christine M. Lohse,Bradley C. Leibovich,R. Houston Thompson,Kathryn E. Pearce,Anne E. Wiktor,John C. Cheville
出处
期刊:The American Journal of Surgical Pathology [Lippincott Williams & Wilkins]
卷期号:36 (5): 663-670 被引量:111
标识
DOI:10.1097/pas.0b013e31824dd972
摘要

Renal cell carcinoma (RCC) with chromosomal rearrangement of transcription factor for immunoglobulin heavy-chain enhancer 3 (TFE3) at Xp11.2 is a distinct subtype that was initially described in children and has been reported to display an indolent course. Recent reports have identified RCC with TFE3 rearrangements in adults and have suggested a more aggressive course in this population. However, only a few studies have examined these tumors in a large series of consecutively treated adults. We screened 632 RCCs from patients consecutively treated by surgery at a single institution by fluorescence in situ hybridization to detect TFE3 rearrangements. We identified 6 RCCs with TFE3 rearrangement. Patient ages ranged from 25 to 78 years and included 4 women and 2 men. Tumors showed significant histologic variability. Comparison of the clinical and pathologic features between RCCs with TFE3 rearrangements and RCCs without TFE3 rearrangements showed no significant differences. Follow-up period for patients with TFE3-rearranged RCC ranged from 0.8 to 16.5 years, with 4 of 6 dying from the disease. Cancer-specific survival for patients with TFE3-rearranged RCC was significantly worse than for patients with TFE3-rearrangement–negative papillary-type RCC (P<0.001) but not different from that for TFE3-rearrangement–negative clear cell-type RCC. In conclusion, we present an assessment of TFE3 rearrangement status in a large series of adults consecutively treated by surgery for RCC. Our findings confirm that RCCs with TFE3 rearrangement account for only approximately 1% of adult RCCs. The results also suggest that adult RCC with TFE3 rearrangement may be a clinically aggressive tumor.

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