Literature DB >> 30327274

Systemic Treatment of Metastatic Clear Cell Renal Cell Carcinoma in 2018: Current Paradigms, Use of Immunotherapy, and Future Directions.

Aly-Khan A Lalani1, Bradley A McGregor2, Laurence Albiges3, Toni K Choueiri2, Robert Motzer4, Thomas Powles5, Christopher Wood6, Axel Bex7.   

Abstract

CONTEXT: Systemic therapy for metastatic clear cell renal cell carcinoma (mccRCC) has greatly evolved over the last 15yr. More recently, combination strategies involving contemporary immunotherapy have emerged as key opportunities to further shift the treatment landscape.
OBJECTIVE: To review the evidence regarding the efficacy and safety of standard therapeutic options in mccRCC as well as combination immunotherapy options on the horizon. EVIDENCE ACQUISITION: PubMed/Medline, Embase, Web of Knowledge, and Cochrane Library databases were searched up to February 2018 and according to the Preferred Reporting Items for Systematic Reviews and Meta-analyses statement. A narrative review of studies was performed. EVIDENCE SYNTHESIS: Twenty-six studies were included regarding therapies for metastatic RCC including vascular endothelial growth factor (VEGF)-directed therapy (n=9), mTOR inhibitors (n=2), cytokines (n=3), vaccines (n=3), and immune checkpoint inhibitors (ICIs, n=9). VEGF tyrosine kinase inhibitor monotherapy had been the standard therapy, and its use is evolving in the front-line setting with ICIs; cabozantinib provides superior progression-free survival versus sunitinib in intermediate- and poor-risk patients, by International Metastatic RCC Database Consortium criteria. The mTOR therapy is largely inferior to VEGF-directed therapy, although it has a role in combination strategies. Cytokines have largely been replaced in current practice throughout most regions, and vaccines have failed to show improved survival in phase III studies to date. ICIs have now become standard care in untreated patients with intermediate and poor risks, given overall survival benefit seen with CheckMate-214 study; survival data from IMmotion 151 are not yet mature. Several ongoing phase III combination trials, with promising early-phase data, are due to be read out.
CONCLUSIONS: The treatment landscape for mccRCC has evolved since the introduction of VEGF inhibitors. Combination therapies involving checkpoint inhibitors could be the next standard of care. PATIENT
SUMMARY: With the expanding role of immune checkpoint inhibitors in metastatic renal cell carcinoma, the treatment paradigm has shifted to include combination therapy in the untreated setting. As the field advances, the bar has been raised in evaluating ongoing combination strategies.
Copyright © 2018 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Combination therapy; Immunotherapy; PD-1/PD-L1; Renal cell carcinoma; Tyrosine kinase inhibitor

Mesh:

Substances:

Year:  2018        PMID: 30327274     DOI: 10.1016/j.eururo.2018.10.010

Source DB:  PubMed          Journal:  Eur Urol        ISSN: 0302-2838            Impact factor:   20.096


  53 in total

1.  First-line Immuno-Oncology Combination Therapies in Metastatic Renal-cell Carcinoma: Results from the International Metastatic Renal-cell Carcinoma Database Consortium.

Authors:  Shaan Dudani; Jeffrey Graham; J Connor Wells; Ziad Bakouny; Sumanta K Pal; Nazli Dizman; Frede Donskov; Camillo Porta; Guillermo de Velasco; Aaron Hansen; Marco Iafolla; Benoit Beuselinck; Ulka N Vaishampayan; Lori A Wood; Elizabeth Liow; Flora Yan; Takeshi Yuasa; Georg A Bjarnason; Toni K Choueiri; Daniel Y C Heng
Journal:  Eur Urol       Date:  2019-08-22       Impact factor: 20.096

2.  Can immune biomarkers predict benefit from targeted agents in metastatic renal cell carcinoma?

Authors:  Renate Pichler; Manuela Schmidinger
Journal:  Ann Transl Med       Date:  2019-12

Review 3.  A Meta-Analysis Evaluating Clinical Outcomes of Patients with Renal Cell Carcinoma Harboring Chromosome 9P Loss.

Authors:  Vincenzo Di Nunno; Veronica Mollica; Matteo Brunelli; Lidia Gatto; Riccardo Schiavina; Michelangelo Fiorentino; Matteo Santoni; Rodolfo Montironi; Anna Caliò; Albino Eccher; Michele Milella; Guido Martignoni; Eugenio Brunocilla; Francesco Massari
Journal:  Mol Diagn Ther       Date:  2019-10       Impact factor: 4.074

4.  Immunotherapy in Genitourinary Malignancy: Evolution in Revolution or Revolution in Evolution.

Authors:  Kevin Lu; Kun-Yuan Chiu; Chen-Li Cheng
Journal:  Cancer Treat Res       Date:  2022

5.  [Speckle-type POZ protein up-regulates c-Jun protein expression and promotes proliferation and invasion of renal carcinoma cells].

Authors:  L Wu; K Yu; Y Cue; X Zhu; Z Yang; J Ma
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2021-03-25

6.  Gαi1 Promoted Proliferation, Migration and Invasion via Activating the Akt-mTOR/Erk-MAPK Signaling Pathway in Renal Cell Carcinoma.

Authors:  Zhan Chen; Yong Zhang; Xiang Wu; Ji Zhang; Wei Xu; Cheng Shen; Bing Zheng
Journal:  Onco Targets Ther       Date:  2021-05-04       Impact factor: 4.147

7.  High-dose-rate surface brachytherapy as a treatment option for renal cell carcinoma cutaneous metastases.

Authors:  Łukasz Raszewski; Artur J Chyrek; Magdalena Marciniak; Wojciech M Burchardt; Grzegorz M Biele da; Adam Chicheł
Journal:  J Contemp Brachytherapy       Date:  2021-05-07

8.  A Metastasis-Related lncRNA Signature Correlates With the Prognosis in Clear Cell Renal Cell Carcinoma.

Authors:  Qian Dou; Shun Gao; Hua Gan; Zhao Kang; Han Zhang; Yichun Yang; Hang Tong
Journal:  Front Oncol       Date:  2021-06-03       Impact factor: 6.244

9.  A Risk Signature with Autophagy-Related Long Noncoding RNAs for Predicting the Prognosis of Clear Cell Renal Cell Carcinoma: Based on the TCGA Database and Bioinformatics.

Authors:  Yundong Xuan; Weihao Chen; Kan Liu; Yu Gao; Shidong Zuo; Baojun Wang; Xin Ma; Xu Zhang
Journal:  Dis Markers       Date:  2021-05-07       Impact factor: 3.434

10.  KCNN4 is a potential prognostic marker and critical factor affecting the immune status of the tumor microenvironment in kidney renal clear cell carcinoma.

Authors:  Shaohua Chen; Chengbang Wang; Xiaotao Su; Xiaodi Dai; Songheng Li; Zengnan Mo
Journal:  Transl Androl Urol       Date:  2021-06
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.