期刊
BMC UROLOGY
卷 20, 期 1, 页码 -出版社
BMC
DOI: 10.1186/s12894-020-00687-2
关键词
Kidney cancer; Genes; VHL gene; PBRM1 mutation; Metastasis; Pan-cancer panel; Next-generation sequencing
资金
- National R&D Program for Cancer Control [HA17C0039]
- Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHID I) - Ministry of Health & Welfare, Republic of Korea [HI14C1277]
Background This study aimed to assess the feasibility of a pan-cancer panel assay for high-risk renal cell carcinoma (RCC) in the Korean population. We also analyzed the clinical and genetic factors contributing to metastasis in clear cell RCC. Methods Thirty-one patients with advanced RCC who underwent radical nephrectomy were analyzed. A 1.8 Mb multi-cancer panel (including 25 RCC-related genes, such as VHL, PBRM1, SETD2, and MET), comprising 181 target genes, 23 fusion genes, and 45 drug target lesions developed by Seoul National University Hospital, was used for this study. Results We extracted DNA from 30 of the 31 (96.7%) RCC specimens. Twenty-one patients (average age 63.3 +/- 11.3 years) with clear cell RCC, 5 with papillary RCC, 3 with chromophobe RCC, and one patient, each with MiT family translocation carcinoma RCC and succinate dehydrogenase deficiency RCC, were analyzed. The sequencing depth was 430.8 +/- 206.6 and 97 mutations (7.3 +/- 2.7 mutations per patient) were detected. The most commonly mutated genes wereVHL(46%),PBRM1(30%), andBAP1,NOTCH4, andPOLQ(23.33% each). Compared with TNM stage matched data from TCGA of clear cell RCC,VHLandPBRM1are most common in both cohorts. Univariate and multivariate analyses revealed that tumor size (Hazard ratio = 2.47,p = 0.04) andPBRM1(Hazard ratio = 28.69,p = 0.05) were related to metastasis in clear cell RCC. Conclusion The pan-cancer panel comprised of RCC-related genes is a feasible and promising tool to evaluate genetic alterations in advanced RCC. However, large-scale studies and a focus on the clinical utility of this cancer panels is needed.
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