Genetic analysis of primary renal cell carcinoma to determine treatment approaches

被引:2
作者
Stuhler, Viktoria [1 ]
Rausch, Steffen [1 ]
Stenzl, Arnulf [1 ]
Bedke, Jens [1 ,2 ]
机构
[1] Eberhard Karls Univ Tuebingen, Univ Hosp Tuebingen, Dept Urol, Tubingen, Germany
[2] German Canc Consortium DKTK, Partner Site Tuebingen, Tubingen, Germany
关键词
Biomarker; heterogeneity; immune checkpoint inhibition; individualized treatment; renal cell carcinoma; tyrosin kinase inhibitor; ENDOTHELIAL GROWTH-FACTOR; MOLECULAR SUBTYPES; TUMOR VASCULATURE; TARGETED THERAPY; EXPRESSION; CANCER; TRIAL; MICROENVIRONMENT; HETEROGENEITY; ANGIOGENESIS;
D O I
10.1080/23808993.2021.1874822
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: To date, there is no validated predictive biomarker available that guides treatment selection between an immune-based or an anti-VEGF-based regimen in patients with metastatic renal cell carcinoma (mRCC). Here, valid biomarkers could increase the benefit of therapy and thereby safe unnecessary toxicity. Recently, phase II and III clinical trials have shown a correlation between molecular clusters and responses to targeted therapy with tyrosine kinase inhibitors (TKIs), immune checkpoint inhibitors (ICIs) or as combination of both in patients with clear-cell mRCC. Areas covered: This review discusses recent advances in the discovery of predictive biomarkers, highlighting the growing role of genetic analysis for treatment selection and its potential impact on precision medicine in mRCC. In this context, we extensively analyzed the available literature from Pubmed's archives on this topic. Expert opinion: Molecular subclassification which predicts responses to TKI, or ICI therapy is an exciting step toward personalized medicine in mRCC, but this still requires validation. However, intratumoral heterogeneity in relationship to the predictive power of molecular analysis of the primary tumor and circulating tumor DNA is challenging and requires further analysis.
引用
收藏
页码:107 / 115
页数:9
相关论文
共 68 条
[1]   A Mechanism of Hypoxia-Mediated Escape from Adaptive Immunity in Cancer Cells [J].
Barsoum, Ivraym B. ;
Smallwood, Chelsea A. ;
Siemens, D. Robert ;
Graham, Charles H. .
CANCER RESEARCH, 2014, 74 (03) :665-674
[2]   Clear cell renal cell carcinoma with wild-type von Hippel-Lindau gene: a non-existent or new tumour entity? [J].
Batavia, Aashil A. ;
Schraml, Peter ;
Moch, Holger .
HISTOPATHOLOGY, 2019, 74 (01) :60-67
[3]   Updated European Association of Urology Guidelines on Renal Cell Carcinoma: Nivolumab plus Cabozantinib Joins Immune Checkpoint Inhibition Combination Therapies for Treatment-naive Metastatic Clear-Cell Renal Cell Carcinoma [J].
Bedke, Jens ;
Albiges, Laurence ;
Capitanio, Umberto ;
Giles, Rachel H. ;
Hora, Milan ;
Lam, Thomas B. ;
Ljungberg, Borje ;
Marconi, Lorenzo ;
Klatte, Tobias ;
Volpe, Alessandro ;
Abu-Ghanem, Yasmin ;
Dabestani, Saeed ;
Fernandez-Pello, Sergio ;
Hofmann, Fabian ;
Kuusk, Teele ;
Tahbaz, Rana ;
Powles, Thomas ;
Bex, Axel .
EUROPEAN UROLOGY, 2021, 79 (03) :339-342
[4]   Molecular Subtypes of Clear Cell Renal Cell Carcinoma Are Associated with Sunitinib Response in the Metastatic Setting [J].
Beuselinck, Benoit ;
Job, Sylvie ;
Becht, Etienne ;
Karadimou, Alexandra ;
Verkarre, Virginie ;
Couchy, Gabrielle ;
Giraldo, Nicolas ;
Rioux-Leclercq, Nathalie ;
Molinie, Vincent ;
Sibony, Mathilde ;
Elaidi, Reza ;
Teghom, Corinne ;
Patard, Jean-Jacques ;
Mejean, Arnaud ;
Fridman, Wolf Herman ;
Sautes-Fridman, Catherine ;
de Reynies, Aurelien ;
Oudard, Stephane ;
Zucman-Rossi, Jessica .
CLINICAL CANCER RESEARCH, 2015, 21 (06) :1329-1339
[5]   A phase 2, single-arm trial of neoadjuvant axitinb plus avelumab in patients (pts) with localized renal cell carcinoma (RCC) who are at high risk of relapse after nephrectomy (NeoAvAx). [J].
Bex, Axel ;
Van Thienen, Johannes V. ;
Schrier, Mariette ;
Hendricksen, Kees ;
Blank, Christian U. ;
Haanen, John B. A. G. .
JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (15)
[6]   Meta-analysis of Clear Cell Renal Cell Carcinoma Gene Expression Defines a Variant Subgroup and Identifies Gender Influences on Tumor Biology [J].
Brannon, A. Rose ;
Haake, Scott M. ;
Hacker, Kathryn E. ;
Pruthi, Raj S. ;
Wallen, Eric M. ;
Nielsen, Matthew E. ;
Rathmell, W. Kimryn .
EUROPEAN UROLOGY, 2012, 61 (02) :258-268
[7]   Molecular stratification of clear cell renal cell carcinoma by consensus clustering reveals distinct subtypes and survival patterns [J].
Brannon, A. Rose ;
Reddy, Anupama ;
Seiler, Michael ;
Arreola, Alexandra ;
Chen, Shufen ;
Moore, Dominic T. ;
Pruthi, Raj S. ;
Wallen, Eric M. ;
Nielsen, Matthew E. ;
Liu, Huiqing ;
Ljungberg, Borje ;
Zhao, Hongjuan ;
Brooks, James D. ;
Ganesan, Shridar ;
Bhanot, Gyan ;
Rathmell, W. Kimryn .
CANCER RESEARCH, 2010, 70
[8]   Identification and Analysis of In Vivo VEGF Downstream Markers Link VEGF Pathway Activity with Efficacy of Anti-VEGF Therapies [J].
Brauer, MJ ;
Zhuang, GL ;
Schmidt, M ;
Yao, J ;
Wu, XM ;
Kaminker, JS ;
Jurinka, SS ;
Kolumam, G ;
Chung, AS ;
Jubb, A ;
Modrusan, Z ;
Ozawa, T ;
James, CD ;
Phillips, H ;
Haley, B ;
Tam, RNW ;
Clermont, AC ;
Cheng, JH ;
Yang, SX ;
Swain, SM ;
Chen, D ;
Scherer, SJ ;
Koeppen, H ;
Yeh, RF ;
Yue, P ;
Stephan, JP ;
Hegde, P ;
Ferrara, N ;
Singh, M ;
Bais, C .
CLINICAL CANCER RESEARCH, 2013, 19 (13) :3681-3692
[9]   Clinical Validation of PBRM1 Alterations as a Marker of Immune Checkpoint Inhibitor Response in Renal Cell Carcinoma [J].
Braun, David A. ;
Ishii, Yuko ;
Walsh, Alice M. ;
Van Allen, Eliezer M. ;
Wu, Catherine J. ;
Shukla, Sachet A. ;
Choueiri, Toni K. .
JAMA ONCOLOGY, 2019, 5 (11) :1631-1633
[10]   Differential Expression of PD-L1 between Primary and Metastatic Sites in Clear-Cell Renal Cell Carcinoma [J].
Callea, Marcella ;
Albiges, Laurence ;
Gupta, Mamta ;
Cheng, Su-Chun ;
Genega, Elizabeth M. ;
Fay, Andre P. ;
Song, Jiaxi ;
Carvo, Ingrid ;
Bhatt, Rupal S. ;
Atkins, Michael B. ;
Hodi, F. Stephen ;
Choueiri, Toni K. ;
McDermott, David F. ;
Freeman, Gordon J. ;
Signoretti, Sabina .
CANCER IMMUNOLOGY RESEARCH, 2015, 3 (10) :1158-1164