Back to Search
Start Over
Third-line sorafenib after sequential therapy with sunitinib and mTOR inhibitors in metastatic renal cell carcinoma.
- Source :
-
European urology [Eur Urol] 2010 Dec; Vol. 58 (6), pp. 906-11. Date of Electronic Publication: 2010 Sep 24. - Publication Year :
- 2010
-
Abstract
- Background: Sunitinib and everolimus have been approved for first- and second-line treatment, respectively, in metastatic renal cell carcinoma (mRCC). The role of sorafenib, which is approved for second-line treatment after cytokines failure, is presently to be defined.<br />Objective: To determine whether third-line sorafenib after sequential use of sunitinib and mammalian target of rapamycin inhibitors (everolimus or temsirolimus) is feasible and effective.<br />Design, Setting, and Participants: One hundred fifty medical records of patients with mRCC treated with first-line sunitinib between January 2006 and January 2010 were reviewed at four participating centers. Data regarding patients treated with the sequence sunitinib-everolimus or temsirolimus-sorafenib were extracted. Central analysis of radiographic images was performed using RECIST criteria to determine progression-free survival (PFS) and overall response rate (oRR) to sorafenib treatment.<br />Measurements: PFS and oRR to sorafenib were the primary end points. Secondary outcomes were safety and overall survival (OS).<br />Results and Limitations: Thirty-four patients were eligible for the study. A median PFS of 4 mo (range: 3-6 mo) and a median OS of 7 mo since sorafenib treatment (range: 6-10 mo) were reported. Of the patients, 23.5% showed response to sorafenib, with an overall disease control rate (complete responses plus partial responses plus stable disease) of 44%. Selection bias, data incompleteness, and absence of study design are inevitable limitations of the study, although central review can strengthen the quality of presented data.<br />Conclusions: Third-line sorafenib appears to be active and well tolerated in mRCC after first-line sunitinib and second-line everolimus or temsirolimus, with no patients interrupting sorafenib because of toxicity or lack of compliance. Prospective, placebo-controlled trials are completely lacking and are required in this setting.<br /> (Copyright © 2010 European Association of Urology. Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Adult
Aged
Angiogenesis Inhibitors administration & dosage
Antineoplastic Combined Chemotherapy Protocols adverse effects
Benzenesulfonates administration & dosage
Carcinoma, Renal Cell enzymology
Carcinoma, Renal Cell mortality
Carcinoma, Renal Cell secondary
Disease-Free Survival
Everolimus
Feasibility Studies
Female
Humans
Indoles administration & dosage
Italy
Kaplan-Meier Estimate
Kidney Neoplasms enzymology
Kidney Neoplasms mortality
Kidney Neoplasms pathology
Male
Middle Aged
Niacinamide analogs & derivatives
Phenylurea Compounds
Protein Kinase Inhibitors administration & dosage
Pyridines administration & dosage
Pyrroles administration & dosage
Retrospective Studies
Sirolimus administration & dosage
Sirolimus analogs & derivatives
Sorafenib
Sunitinib
Survival Rate
TOR Serine-Threonine Kinases metabolism
Time Factors
Treatment Outcome
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Carcinoma, Renal Cell drug therapy
Kidney Neoplasms drug therapy
TOR Serine-Threonine Kinases antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1873-7560
- Volume :
- 58
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- European urology
- Publication Type :
- Academic Journal
- Accession number :
- 20884115
- Full Text :
- https://doi.org/10.1016/j.eururo.2010.09.008