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Bevacizumab in combination with IFN-α in metastatic renal cell carcinoma: the AVOREN trial
B. Melichar, H. Procházková-Študentová, D. Vitásková,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, přehledy
NLK
ProQuest Central
od 2001-06-01 do 2014-09-30
Health & Medicine (ProQuest)
od 2001-06-01 do 2014-09-30
Public Health Database (ProQuest)
od 2001-06-01 do 2014-09-30
PubMed
23136836
DOI
10.1586/era.12.103
Knihovny.cz E-zdroje
- MeSH
- humanizované monoklonální protilátky aplikace a dávkování MeSH
- interferon alfa aplikace a dávkování MeSH
- karcinom z renálních buněk farmakoterapie MeSH
- klinické zkoušky, fáze II jako téma MeSH
- klinické zkoušky, fáze III jako téma MeSH
- lidé MeSH
- nádory ledvin farmakoterapie MeSH
- přežití bez známek nemoci MeSH
- protokoly protinádorové kombinované chemoterapie terapeutické užití MeSH
- randomizované kontrolované studie jako téma MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Metastatic renal cell carcinoma (mRCC) is tumor resistant to all cytotoxic agents. During the last decade, effective targeted therapies emerged including sunitinib, pazopanib and the combination of bevacizumab with IFN-α. The use of bevacizumab plus IFN-α combination in mRCC is supported by the AVOREN trial. Although the primary end point of the AVOREN trial was overall survival, progression-free survival was used to evaluate efficacy and served as the basis of regulatory submission owing to the advent of targeted agents that probably resulted in the prolongation of overall survival in both experimental and control arms. The doubling of median progression-free survival in the AVOREN trials (from 5.4 to 10.2 months) is remarkably similar compared with the results of Phase III trials with sunitinib and pazopanib. Bevacizumab plus IFN-α is the only combined regimen currently used in mRCC and serves as a comparator in the trials combining bevacizumab with other agents.
Citace poskytuje Crossref.org
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