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1789 PREDICTION OF TKI-THERAPY RESPONSE IN PATIENTS WITH METASTATIC RENAL CELL CARCINOMA BY SERUM PROTEOMICS
- Source :
- Journal of Urology. 187
- Publication Year :
- 2012
- Publisher :
- Ovid Technologies (Wolters Kluwer Health), 2012.
-
Abstract
- p44/42 mitogen-activated protein kinase (MAPK) and signal transducers and activation of transcription 3 (STAT3), vascular endothelial growth factor receptor (VEGFR)-1 and -2, and platelet-derived growth factor receptor (PDGFR)and , in primary RCC specimens were measured by immunohistochemical staining. RESULTS: Of several factors examined, tumor grade and the expression level of VEGFR-2 were shown to have significant impact on response to sunitinib in these 60 patients. Progression-free survival (PFS) was significantly associated with the expression levels of VEGFR-2 in addition to tumor grade, performance status, MSKCC risk classification system and c-reactive protein level on univariate analysis. Of these significant factors, only VEGFR-2 expression appeared to be independently related to PFS by multivariate analysis. In fact, the PFS in patients with strong expression of VEGFR-2 was significantly favorable compared with that in those with weak expression of VEGFR-2. CONCLUSIONS: It would be useful to consider expression levels of potential molecular markers, particularly VEGFR-2, as well as conventional parameters to select metastatic RCC patients likely to benefit from treatment with sunitinib.
- Subjects :
- Oncology
medicine.medical_specialty
Univariate analysis
biology
Performance status
Sunitinib
business.industry
Urology
medicine.disease
Growth factor receptor
Renal cell carcinoma
Internal medicine
embryonic structures
medicine
biology.protein
Immunohistochemistry
STAT3
business
Platelet-derived growth factor receptor
medicine.drug
Subjects
Details
- ISSN :
- 15273792 and 00225347
- Volume :
- 187
- Database :
- OpenAIRE
- Journal :
- Journal of Urology
- Accession number :
- edsair.doi...........8bb410619f1ecb85b880d91b895477a8
- Full Text :
- https://doi.org/10.1016/j.juro.2012.02.1820