Title of article
mTOR pathway inhibition in renal cell carcinoma
Author/Authors
Pinto Marيn، نويسنده , , Alvaro and Redondo Sلnchez، نويسنده , , Andrés and Espinosa Arranz، نويسنده , , Enrique and Zamora Auٌَn، نويسنده , , Pilar and Castelo Fernلndez، نويسنده , , Beatriz and Gonzلlez Barَn، نويسنده , , Manuel، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2012
Pages
6
From page
356
To page
361
Abstract
Renal cell carcinoma therapy has changed in a very significant way in the last few years. Up to 5 new agents have been developed, improving the results previously achieved with cytokine therapy. Bevacizumab, sorafenib, sunitinib, temsirolimus, and everolimus are now part of the therapeutic arsenal for this illness. Particularly, this has been the first tumoral type in which inhibition of mammalian target of rapamycin (mTOR) has proved its efficacy in phase III trials, either as first-line therapy for poor prognosis patients (temsirolimus, CCI-779) or as second-line therapy after failure of tyrosine-kinase inhibitors (everolimus, RAD001). In this paper, we review the basis for mTOR inhibition in RCC, and discuss the results of the trials involving temsirolimus and everolimus for the treatment of this disease.
Keywords
renal cell carcinoma , mTOR , Temsirolimus , Everolimus
Journal title
Urologic Oncology
Serial Year
2012
Journal title
Urologic Oncology
Record number
1890592
Link To Document