Literature DB >> 26036356

New molecular targets in non clear renal cell carcinoma: An overview of ongoing clinical trials.

Chiara Ciccarese1, Francesco Massari1, Matteo Santoni2, Daniel Y C Heng3, Valeria Sotte4, Matteo Brunelli5, Alessandro Conti6, Liang Cheng7, Antonio Lopez-Beltran8, Marina Scarpelli9, Stefano Cascinu4, Giampaolo Tortora1, Rodolfo Montironi9.   

Abstract

Non-clear cell renal cell carcinomas (nccRCCs) are a heterogeneous group of tumors, characterized by different histological features, molecular alterations, clinical outcomes, and responses to treatment. According to the 2004 WHO classification, 50 different histotypes were recognized. In 2013, five new distinct epithelial tumors and three provisional entities have been added to this classification, relying on morphology, immunohistochemistry, cytogenetics, and molecular pathology advances. Targeted therapies against VEGF and mTOR pathways have become the cornerstones of the treatment for clear cell RCC, dramatically revolutionizing the patients' prognosis. Interestingly, other than mTOR and VEGF pathways, tumor proliferation of some nccRCC histotypes seems to depend on alternative signaling pathways, as demonstrated by the close correlation between papillary RCC and activation of the HGF/MET axis. Currently, several strategies are under evaluation in patients with nccRCC. These approaches include TKIs and mTOR inhibitors, MET-pathway antagonists and immunotherapy. The aim of this review is to analyze the rationale for the use of TKIs and mTOR inhibitors as treatment options for nccRCC and to describe the future therapeutic perspectives for these patients.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Clinical trials; Immunotherapy; Non clear cell renal cell carcinoma; Prognosis; Tyrosine kinase inhibitors

Mesh:

Year:  2015        PMID: 26036356     DOI: 10.1016/j.ctrv.2015.05.006

Source DB:  PubMed          Journal:  Cancer Treat Rev        ISSN: 0305-7372            Impact factor:   12.111


  8 in total

1.  IL-6 is involved in malignancy and doxorubicin sensitivity of renal carcinoma cells.

Authors:  Yanqiang Chen; Jianzhen Liu; Pei Lv; Jiangyan Gao; Mingzheng Wang; Yongjun Wang
Journal:  Cell Adh Migr       Date:  2017-06-19       Impact factor: 3.405

2.  TAMing resistance to multi-targeted kinase inhibitors through Axl and Met inhibition.

Authors:  D J Pinato; S Chowdhury; J Stebbing
Journal:  Oncogene       Date:  2015-10-05       Impact factor: 9.867

3.  Plasma cytokine and angiogenic factors associated with prognosis and therapeutic response to sunitinib vs everolimus in advanced non-clear cell renal cell carcinoma.

Authors:  Pavlos Msaouel; Amado J Zurita; Shixia Huang; Eric Jonasch; Nizar M Tannir
Journal:  Oncotarget       Date:  2017-06-27

Review 4.  Beyond evidence-based data: scientific rationale and tumor behavior to drive sequential and personalized therapeutic strategies for the treatment of metastatic renal cell carcinoma.

Authors:  Lorena Incorvaia; Giuseppe Bronte; Viviana Bazan; Giuseppe Badalamenti; Sergio Rizzo; Gianni Pantuso; Clara Natoli; Antonio Russo
Journal:  Oncotarget       Date:  2016-04-19

Review 5.  Long-term efficacy of crizotinib in a metastatic papillary renal carcinoma with MET amplification: a case report and literature review.

Authors:  Philippe Rochigneux; Jeanne Thomassin-Piana; Sophy Laibe; Serge Brunelle; Naji Salem; Bernard Escudier; Gilles Vassal; Gwenaelle Gravis
Journal:  BMC Cancer       Date:  2018-11-22       Impact factor: 4.430

6.  The value of hepatic resection in metastasic renal cancer in the Era of Tyrosinkinase Inhibitor Therapy.

Authors:  Hans Michael Hau; Florian Thalmann; Christoph Lübbert; Mehmet Haluk Morgul; Moritz Schmelzle; Georgi Atanasov; Christian Benzing; Undine Lange; Rudolf Ascherl; Roman Ganzer; Dirk Uhlmann; Hans-Michael Tautenhahn; Georg Wiltberger; Michael Bartels
Journal:  BMC Surg       Date:  2016-07-22       Impact factor: 2.102

7.  Modulating ATP binding cassette transporters in papillary renal cell carcinoma type 2 enhances its response to targeted molecular therapy.

Authors:  Rola M Saleeb; Mina Farag; Zsuzsanna Lichner; Fadi Brimo; Jenni Bartlett; Georg Bjarnason; Antonio Finelli; Fabio Rontondo; Michelle R Downes; George M Yousef
Journal:  Mol Oncol       Date:  2018-08-23       Impact factor: 6.603

8.  microRNA-505 negatively regulates HMGB1 to suppress cell proliferation in renal cell carcinoma.

Authors:  Bing Zhong; Zhiqiang Qin; Hui Zhou; Fengming Yang; Ke Wei; Xi Jiang; Ruipeng Jia
Journal:  J Cell Physiol       Date:  2019-01-15       Impact factor: 6.384

  8 in total

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