Literature DB >> 27807302

Sunitinib: Ten Years of Successful Clinical Use and Study in Advanced Renal Cell Carcinoma.

Robert J Motzer1, Bernard Escudier2, Andrew Gannon3, Robert A Figlin4.   

Abstract

The oral multikinase inhibitor sunitinib malate was approved by the U.S. Food and Drug Administration in January 2006 for use in patients with advanced renal cell carcinoma (RCC). Since then, it has been approved globally for this indication and for patients with imatinib-resistant or -intolerant gastrointestinal stromal tumors and advanced pancreatic neuroendocrine tumors. As we mark the 10-year anniversary of the beginning of the era of targeted therapy, and specifically the approval of sunitinib, it is worthwhile to highlight the progress that has been made in advanced RCC as it relates to the study of sunitinib. We present the key trials and data for sunitinib that established it as a reference standard of care for first-line advanced RCC therapy and, along with other targeted agents, significantly altered the treatment landscape in RCC. Moreover, we discuss the research with sunitinib that has sought to refine its role via patient selection and prognostic markers, improve dosing and adverse event management, and identify predictive efficacy biomarkers, plus the extent to which this research has contributed to the overall understanding and management of RCC. We also explore the key learnings regarding study design and data interpretation from the sunitinib studies and how these findings and the sunitinib development program, in general, can be a model for successful development of other agents. Finally, ongoing research into the continued and future role of sunitinib in RCC management is discussed. THE ONCOLOGIST: 2017;22:41-52 IMPLICATIONS FOR PRACTICE: Approved globally, sunitinib is established as a standard of care for first-line advanced renal cell carcinoma (RCC) therapy and, along with other targeted agents, has significantly altered the treatment landscape in RCC. Research with sunitinib that has sought to refine its role via patient selection and prognostic markers, improve dosing and adverse event management, and identify predictive efficacy biomarkers has contributed to the overall understanding and management of RCC. Key learnings regarding study design and data interpretation from the sunitinib studies and the sunitinib development program, in general, can be a model for the successful development of other agents. © AlphaMed Press 2016.

Entities:  

Keywords:  Drug development; Renal cell carcinoma; Study design; Sunitinib; Treatment management

Mesh:

Substances:

Year:  2016        PMID: 27807302      PMCID: PMC5313263          DOI: 10.1634/theoncologist.2016-0197

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  92 in total

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Authors:  Frede Donskov; M Dror Michaelson; Igor Puzanov; Mellar P Davis; Georg A Bjarnason; Robert J Motzer; David Goldstein; Xun Lin; Darrel P Cohen; Robin Wiltshire; Brian I Rini
Journal:  Br J Cancer       Date:  2015-10-22       Impact factor: 7.640

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Journal:  Cancer Metastasis Rev       Date:  2021-01-07       Impact factor: 9.264

2.  Diclofenac sex-divergent drug-drug interaction with Sunitinib: pharmacokinetics and tissue distribution in male and female mice.

Authors:  Chii Chii Chew; Salby Ng; Yun Lee Chee; Teng Wai Koo; Ming Hui Liew; Evelyn Li-Ching Chee; Pilar Modamio; Cecilia Fernández; Eduardo L Mariño; Ignacio Segarra
Journal:  Invest New Drugs       Date:  2017-03-11       Impact factor: 3.850

3.  Anlotinib Versus Sunitinib as First-Line Treatment for Metastatic Renal Cell Carcinoma: A Randomized Phase II Clinical Trial.

Authors:  Ai-Ping Zhou; Yuxian Bai; Yan Song; Hong Luo; Xiu-Bao Ren; Xiuwen Wang; Benkang Shi; Cheng Fu; Ying Cheng; Jiyan Liu; Shukui Qin; Jun Li; Hanzhong Li; Xianzhong Bai; Dingwei Ye; Jinwan Wang; Jianhui Ma
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4.  C1QBP regulates apoptosis of renal cell carcinoma via modulating xanthine dehydrogenase (XDH) mediated ROS generation.

Authors:  Yiting Wang; Shuang Liu; Shaoping Tian; Runxuan Du; Tianyu Lin; Xuesong Xiao; Rui Wang; Ruibing Chen; Hua Geng; Saravanan Subramanian; Yuanjie Niu; Yong Wang; Dan Yue
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5.  The pharmacokinetic interaction between irinotecan and sunitinib.

Authors:  Lili Jiang; Li Wang; Zhongmin Zhang; Zhen Wang; Xiaoyu Wang; Shujuan Wang; Xiaowei Luan; Yangliu Xia; Yong Liu
Journal:  Cancer Chemother Pharmacol       Date:  2019-11-05       Impact factor: 3.333

Review 6.  Small molecules in targeted cancer therapy: advances, challenges, and future perspectives.

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Journal:  Signal Transduct Target Ther       Date:  2021-05-31

Review 7.  Sex-Divergent Clinical Outcomes and Precision Medicine: An Important New Role for Institutional Review Boards and Research Ethics Committees.

Authors:  Ignacio Segarra; Pilar Modamio; Cecilia Fernández; Eduardo L Mariño
Journal:  Front Pharmacol       Date:  2017-07-21       Impact factor: 5.810

8.  The tyrosine-kinase inhibitor sunitinib targets vascular endothelial (VE)-cadherin: a marker of response to antitumoural treatment in metastatic renal cell carcinoma.

Authors:  Helena Polena; Julie Creuzet; Maeva Dufies; Adama Sidibé; Abir Khalil-Mgharbel; Aude Salomon; Alban Deroux; Jean-Louis Quesada; Caroline Roelants; Odile Filhol; Claude Cochet; Ellen Blanc; Céline Ferlay-Segura; Delphine Borchiellini; Jean-Marc Ferrero; Bernard Escudier; Sylvie Négrier; Gilles Pages; Isabelle Vilgrain
Journal:  Br J Cancer       Date:  2018-03-22       Impact factor: 7.640

9.  A Neuroprotective Dose of Isatin Causes Multilevel Changes Involving the Brain Proteome: Prospects for Further Research.

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Journal:  Int J Mol Sci       Date:  2020-06-11       Impact factor: 5.923

10.  Health and kinship matter: Learning about direct-to-consumer genetic testing user experiences via online discussions.

Authors:  Zhijun Yin; Lijun Song; Ellen W Clayton; Bradley A Malin
Journal:  PLoS One       Date:  2020-09-08       Impact factor: 3.240

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