Complexity of the genomic landscape of renal cell carcinoma: Implications for targeted therapy and precision immuno-oncology

被引:16
作者
Sanfrancesco, Joseph M. [1 ]
Cheng, Liang [1 ,2 ]
机构
[1] Indiana Univ Sch Med, Dept Pathol & Lab Med, 350 West 11th St,IUHPL Room 4010, Indianapolis, IN 46202 USA
[2] Indiana Univ Sch Med, Dept Urol, Indianapolis, IN 46202 USA
关键词
Kidney; Tumor heterogeneity; Renal cell carcinoma; Clonal evolution; Targeted therapy; Precision immuno-oncology; SARCOMATOID TRANSFORMATION; INTRATUMOR HETEROGENEITY; ADJUVANT SUNITINIB; UNTREATED MELANOMA; SYSTEMIC THERAPY; PHASE-3; TRIAL; HIGH-RISK; NIVOLUMAB; CANCER; EVOLUTION;
D O I
10.1016/j.critrevonc.2017.09.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The topic of tumoral heterogeneity at the genetic level has become relevant in various solid origin tumors, particularly in an age of targeted treatment. Renal cell carcinoma is known for a sizable subset of tumors presenting at advanced clinical stage, further highlighting the importance and timeliness of this topic and its potential impact on adjuvant therapy. Recent studies have shown that molecular aberrations in renal cell carcinoma go beyond known truncal mutations and that downstream, subclonal aberrations are spatially heterogenous. Intratumoral heterogeneity as well as the differences in the molecular landscape between primary and metastatic lesions remains underappreciated, often due to inadequate sampling of tumors. The overall effect of these factors on the efficacy of current treatment options in renal cell carcinoma remains unknown; however, several recent studies have attempted to elucidate the extent and impact genetic heterogeneity in renal cell neoplasia may have on patient treatment and prognosis.
引用
收藏
页码:23 / 28
页数:6
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