Literature DB >> 28952411

Clinical development of mTor inhibitors for renal cancer.

Michele Ghidini1, Fausto Petrelli2, Antonio Ghidini3, Gianluca Tomasello1, Jens Claus Hahne4, Rodolfo Passalacqua1, Sandro Barni2.   

Abstract

INTRODUCTION: Renal cell carcinoma (RCC) accounts for approximately 3% of adult malignancies and 90-95% of neoplasms arising from the kidney. In the last 10 years, clinical trials have established multitargeted tyrosine kinase inhibitors (TKIs) as the standard first-line treatment in patients with metastatic disease. Multiple agents are now available for treatment in subsequent lines.The mammalian target of rapamycin (mTOR) inhibitors (e.g., everolimus alone or with lenvatinib) are among the most effective options. Areas covered: This paper provides a complete and updated overview on mTOR inhibitors for the treatment of advanced RCC. The authors revised the results of the most recent completed clinical trials and provided information about ongoing trials. Expert opinion: mTOR pathway still represents an important driver for RCC management. Combination of everolimus and lenvatinib is considered a category 1 choice with cabozantinib and nivolumab for subsequent therapy in metastatic RCC according to NCCN guidelines v2.2017. These three treatments (levantinib/everolimus, cabozantinib, and nivolumab) all resulted in a superior efficacy compared to everolimus alone. Moreover, mTOR inhibitors, and in particular temsirolimus for poor risk patients, are available choices for treatment in non-clear cell carcinomas together with TKIs.

Entities:  

Keywords:  advanced disease; everolimus; mTOR inhibitors; renal cell carcinoma; temsirolimus

Mesh:

Substances:

Year:  2017        PMID: 28952411     DOI: 10.1080/13543784.2017.1384813

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  14 in total

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Journal:  Oncoimmunology       Date:  2018-02-15       Impact factor: 8.110

Review 2.  Therapeutic potential of CDK4/6 inhibitors in renal cell carcinoma.

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Review 4.  Receptor tyrosine kinases and downstream pathways as druggable targets for cancer treatment: the current arsenal of inhibitors.

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Review 5.  Crosstalk between VEGFR and other receptor tyrosine kinases for TKI therapy of metastatic renal cell carcinoma.

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Journal:  Cancer Cell Int       Date:  2018-03-05       Impact factor: 5.722

6.  Pathway Based Analysis of Mutation Data Is Efficient for Scoring Target Cancer Drugs.

Authors:  Marianna A Zolotovskaia; Maxim I Sorokin; Anna A Emelianova; Nikolay M Borisov; Denis V Kuzmin; Pieter Borger; Andrew V Garazha; Anton A Buzdin
Journal:  Front Pharmacol       Date:  2019-01-23       Impact factor: 5.810

Review 7.  Autophagy Modulators: Mechanistic Aspects and Drug Delivery Systems.

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Journal:  Biomolecules       Date:  2019-09-25

Review 8.  Highlights in Resistance Mechanism Pathways for Combination Therapy.

Authors:  João M A Delou; Alana S O Souza; Leonel C M Souza; Helena L Borges
Journal:  Cells       Date:  2019-08-30       Impact factor: 6.600

9.  Prognostic significance of PI3K/AKT/ mTOR signaling pathway members in clear cell renal cell carcinoma.

Authors:  Demin Fan; Qiang Liu; Fei Wu; Na Liu; Hongyi Qu; Yijiao Yuan; Yong Li; Huayu Gao; Juntao Ge; Yue Xu; Hao Wang; Qingyong Liu; Zuohui Zhao
Journal:  PeerJ       Date:  2020-06-01       Impact factor: 2.984

Review 10.  The emerging roles of protein homeostasis-governing pathways in Alzheimer's disease.

Authors:  Ji Cheng; Brian J North; Tao Zhang; Xiangpeng Dai; Kaixiong Tao; Jianping Guo; Wenyi Wei
Journal:  Aging Cell       Date:  2018-07-10       Impact factor: 9.304

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