Racial Disparities in MiT Family Translocation Renal Cell Carcinoma

Author:

Lu Xiaofan1ORCID,Tawanaie Pour Sedehi Nassim1,Su Xiaoping2ORCID,Yan Fangrong3ORCID,Alhalabi Omar4ORCID,Tannir Nizar M4ORCID,Malouf Gabriel G15ORCID

Affiliation:

1. Department of Cancer and Functional Genomics, Institute of Genetics and Molecular and Cellular Biology, CNRS/INSERM/UNISTRA , Illkirch , France

2. Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center , Houston, TX , USA

3. Research Center of Biostatistics and Computational Pharmacy, China Pharmaceutical University , Nanjing , People’s Republic of China

4. Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center , Houston, TX , USA

5. Department of Medical Oncology, Institut de Cancérologie de Strasbourg, Strasbourg University , Strasbourg , France

Abstract

Abstract Racial disparities have been documented in the biology and outcome of certain renal cell carcinomas (RCCs) among Black patients. However, little is known about racial differences in MiT family translocation RCC (TRCC). To investigate this issue, we performed a case-control study using data from The Cancer Genome Atlas (TCGA) and the Chinese OrigiMed2020 cohort. A total of 676 patients with RCC (14 Asian, 113 Black, and 525 White) were identified in TCGA, and TRCC was defined as RCC with TFE3/TFEB translocation or TFEB amplification, leading to 21 patients with TRCC (2 Asian, 8 Black, 10 White, and 1 unknown). Asian (2 of 14 [14.3%] vs 10 of 525 [1.9%]; P = .036) and Black (8 of 113 [7.1%] vs 1.9%; P = .007) patients with RCC showed significantly higher prevalence of TRCC compared with White patients with RCC. The overall mortality rate of TRCC was slightly higher in Asian and Black patients compared with White patients (HR: 6.05, P = .069). OrigiMed2020 Chinese patients with RCC had a significantly higher proportion of TRCC with TFE3 fusions than TCGA White patients with RCC (13 of 250 [5.2%] vs 7 of 525 [1.3%]; P = .003). Black patients with TRCC were more likely to exhibit the proliferative subtype than White patients (6 of 8 [75%] vs 2 of 9 [22.2%]; P = .057) for those who had RNA-seq profiles. We present evidence of higher prevalence of TRCC in Asian and Black patients with RCC compared with White patients and show that these tumors in Asian and Black patients have distinct transcriptional signatures and are associated with poor outcomes.

Funder

National Natural Science Foundation of China

Key R&D Program of Jiangsu Province

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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