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Cited by 454

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Targeted Therapy for Metastatic Renal Cell Carcinoma

Motzer, Robert J., Bukowski, Ronald M.·2006·Journal of Clinical Oncology

Abstract

The discovery of a relationship for the VHL tumor suppressor gene, hypoxia inducible factor-1 alpha, and vascular endothelial growth factor in the growth of clear-cell renal cell carcinoma (RCC) has identified a pathway for novel targeted therapy. This study evaluated the impact of these agents on metastatic RCC (mRCC), and highlights recent phase II and III trials. A systematic review examined the clinical data for novel targeted agents in mRCC, with a focus on randomized phase II and III trials of the novel targeted agents sunitinib, temsirolimus, sorafenib, and bevacizumab. Several agents, including the small-molecule targeted inhibitors sunitinib, temsirolimus, sorafenib, and the monoclonal antibody bevacizumab, have demonstrated antitumor activity in randomized trials. Superior activity was found with sunitinib and temsirolimus versus cytokines in first-line therapy. Improved progression-free survival was reported with sorafenib and bevacizumab given second-line compared with placebo. Targeted therapies show promising activity in this disease, and they have been changing patient management. Sunitinib and sorafenib were recently approved by the US Food and Drug Administration for treatment of mRCC, These drugs are currently included in clinical practice.

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Crossref · 10.1200/jco.2006.08.5415

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Metadata

Authors
Motzer, R. J., & Bukowski, R. M.
Venue
Journal of Clinical Oncology
Published
2006-12-10
Volume
24
Issue
35
Pages
5601-5608
ISSN
  • 0732-183X (ISSN-L)
  • 1527-7755
OpenAlex
W2097976367
Cited by
454
References
3
FWCI
50.45
Type
journal article
Language
en
Open access
closed

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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