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Angiotensin system inhibitors and survival outcomes in patients with metastatic renal cell carcinoma.
McKay, Rana R; Rodriguez, Gustavo E; Lin, Xun; Kaymakcalan, Marina D; Hamnvik, Ole-Petter R; Sabbisetti, Venkata S; Bhatt, Rupal S; Simantov, Ronit; Choueiri, Toni K.
Afiliação
  • McKay RR; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Rodriguez GE; Pfizer Oncology, Pfizer Inc., New York, New York.
  • Lin X; Division of Endocrinology, Diabetes, and Hypertension, Brigham and Woman's Hospital, Boston, Massachusetts.
  • Kaymakcalan MD; Department of Pharmacy and Clinical Support, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Hamnvik OP; Division of Endocrinology, Diabetes, and Hypertension, Brigham and Woman's Hospital, Boston, Massachusetts.
  • Sabbisetti VS; Department of Nephrology, Brigham and Woman's Hospital, Boston, Massachusetts.
  • Bhatt RS; Division of Hematology-Oncology and Cancer Biology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
  • Simantov R; Pfizer Oncology, Pfizer Inc., New York, New York.
  • Choueiri TK; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts. toni_choueiri@DFCI.harvard.edu.
Clin Cancer Res ; 21(11): 2471-9, 2015 Jun 01.
Article em En | MEDLINE | ID: mdl-25724518
PURPOSE: The renin-angiotensin system may play a role in carcinogenesis. The purpose of this study was to evaluate the impact of angiotensin system inhibitors (ASI) on outcomes in metastatic renal cell carcinoma (mRCC) patients treated in the targeted therapy era. EXPERIMENTAL DESIGN: We conducted a pooled analysis of mRCC patients treated on phase II and III clinical trials. Statistical analyses were performed using Cox regression adjusted for several risk factors and the Kaplan-Meier method. RESULTS: A total of 4,736 patients were included, of whom 1,487 received ASIs and 783 received other antihypertensive agents. Overall, ASI users demonstrated improved overall survival (OS) compared with users of other antihypertensive agents (adjusted HR, 0.838, P = 0.0105, 26.68 vs. 18.07 months) and individuals receiving no antihypertensive therapy (adjusted HR, 0.810, P = 0.0026, 26.68 vs. 16.72 months). When stratified by therapy type, a benefit in OS was demonstrated in ASI users compared with nonusers in individuals receiving VEGF therapy (adjusted HR, 0.737, P < 0.0001, 31.12 vs. 21.94 months) but not temsirolimus or IFNα. An in vitro cell viability assay demonstrated that sunitinib in combination with an ASI significantly decreased RCC cell viability compared with control at physiologically relevant doses. This effect was not observed with either agent alone or with other non-ASI antihypertensives or temsirolimus. CONCLUSIONS: In the largest analysis to date, we demonstrate that ASI use improved survival in mRCC patients treated in the targeted therapy era. Further studies are warranted to investigate the mechanism underlying this interaction and verify our observations to inform clinical practice.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema Renina-Angiotensina / Angiotensinas / Carcinoma de Células Renais Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2015 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema Renina-Angiotensina / Angiotensinas / Carcinoma de Células Renais Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2015 Tipo de documento: Article País de publicação: Estados Unidos