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Survival Outcomes and Tumor IMP3 Expression in Patients with Sarcomatoid Metastatic Renal Cell Carcinoma.
Tantravahi, Srinivas K; Albertson, Daniel; Agarwal, Archana M; Ravulapati, Sowmya; Poole, Austin; Patel, Shiven B; Hawatmeh, Jamil S; Straubhar, Alli M; Liu, Ting; Stenehjem, David D; Agarwal, Neeraj.
Afiliación
  • Tantravahi SK; Department of Internal Medicine, University of Utah Huntsman Cancer Institute, Salt Lake City, UT 84112, USA.
  • Albertson D; ARUP Laboratories, Department of Pathology, The University of Utah, Salt Lake City, UT 84108, USA.
  • Agarwal AM; ARUP Laboratories, Department of Pathology, The University of Utah, Salt Lake City, UT 84108, USA.
  • Ravulapati S; Department of Internal Medicine, University of Utah Huntsman Cancer Institute, Salt Lake City, UT 84112, USA.
  • Poole A; Department of Internal Medicine, University of Utah Huntsman Cancer Institute, Salt Lake City, UT 84112, USA.
  • Patel SB; Department of Internal Medicine, University of Utah Huntsman Cancer Institute, Salt Lake City, UT 84112, USA.
  • Hawatmeh JS; Department of Internal Medicine, University of Utah Huntsman Cancer Institute, Salt Lake City, UT 84112, USA.
  • Straubhar AM; Department of Internal Medicine, University of Utah Huntsman Cancer Institute, Salt Lake City, UT 84112, USA.
  • Liu T; ARUP Laboratories, Department of Pathology, The University of Utah, Salt Lake City, UT 84108, USA.
  • Stenehjem DD; Pharmacotherapy Outcomes Research Center (PORC), College of Pharmacy, The University of Utah, Salt Lake City, UT 84112, USA.
  • Agarwal N; Department of Internal Medicine, University of Utah Huntsman Cancer Institute, Salt Lake City, UT 84112, USA.
J Oncol ; 2015: 181926, 2015.
Article en En | MEDLINE | ID: mdl-25688268
Metastatic renal cell carcinoma with sarcomatoid histology (SmRCC) is associated with poor survival. No data is available from randomized trials on the efficacy of vascular endothelial growth factor (VEGF) and mammalian target of rapamycin (mTOR) inhibitors in SmRCC. We identified SmRCC patients from a single institutional database. To identify predictive and prognostic biomarkers, immunohistochemistry (IHC) analysis was performed on the tumor samples for downstream targets of VEGF and mTOR pathways. Survival outcomes were stratified by IHC analysis, extent of sarcomatoid component, Memorial Sloan-Kettering Cancer Center (MSKCC), and Heng risk criteria. Twenty-seven patients with SmRCC were included. First line therapy included targeted therapy (n = 19), immunotherapy (n = 4), cytotoxic chemotherapy (n = 1), and no treatment (n = 3). Median OS was 8.2 months (95% CI 3.8-14.2 months). Median survival in months, based on MSKCC and Heng risk groups, was favorable 89.3 versus 84.5, intermediate 9.5 versus 12.7, and poor 3.9 versus 5.1. None of the IHC markers predicted outcomes of treatment with VEGF or mTOR inhibitors. Only tumor IMP3 expression was associated with inferior OS, although not statistically significant (IMP3 negative 14.2 versus IMP3 positive 4.9 months; HR 0.46, 95% CI 0.16-1.21; P = 0.12). The study was limited by small sample size.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies Idioma: En Revista: J Oncol Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies Idioma: En Revista: J Oncol Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos