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PMID: 25681967 Published · ppublish English Comparative Study Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Validation Study

The International Metastatic Renal Cell Carcinoma Database Consortium model as a prognostic tool in patients with metastatic renal cell carcinoma previously treated with first-line targeted therapy: a population-based study.

The Lancet. Oncology ·Vol. 16 ·No. 3 ·2015-03-00 ·Pages 293-300

Ko JJ, Xie W, Kroeger N, Lee JL, Rini BI, Knox JJ, Bjarnason GA, Srinivas S, Pal SK, Yuasa T, Smoragiewicz M, Donskov F, Kanesvaran R, Wood L, Ernst DS, Agarwal N, Vaishampayan UN, Rha SY, Choueiri TK, Heng DY

Abstract

Previous prognostic models for second-line systemic therapy in patients with metastatic renal cell carcinoma have not been studied in the setting of targeted therapy. We sought to validate the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) model in patients with metastatic renal cell carcinoma receiving next-line targeted therapy after progression on first-line targeted therapy. In this population-based study, we analysed patients who received second-line targeted therapy for metastatic renal cell carcinoma at 19 centres in Canada, USA, Greece, Japan, Singapore, South Korea, and Denmark. The primary endpoint was overall survival since the initiation of second-line therapy. We compared the prognostic performance of the IMDC model with the three-factor MSKCC model used for previously treated patients for overall survival since the start of second-line targeted therapy. Between Jan 1, 2005, and Nov 30, 2012, we included 1021 patients treated with second-line targeted therapy. Median overall survival since the start of second-line targeted therapy was 12·5 months (95% CI 11·3-14·3). Five of six predefined factors in the IMDC model (anaemia, thrombocytosis, neutrophilia, Karnofsky performance status [KPS] <80, and <1 year from diagnosis to first-line targeted therapy) were independent predictors of poor overall survival on multivariable analysis. The concordance index using all six prognostic factors (ie, also including hypercalcaemia) was 0·70 (95% CI 0·67-0·72) with the IMDC model and was 0·66 (95% CI 0·64-0·68) with the three-factor MSKCC model. When patients were divided into three risk categories using IMDC criteria, median overall survival was 35·3 months (95% CI 28·3-47·8) in the favourable risk group (n=76), 16·6 months (14·9-17·9) in the intermediate risk group (n=529), and 5·4 months (4·7-6·8) in the poor risk group (n=261). The IMDC prognostic model can be applied to patients previously treated with targeted therapy, in addition to previously validated populations in first-line targeted therapy. The IMDC prognostic model in the second-line targeted therapy setting has an improved prognostic performance and is applicable to a more contemporary patient cohort than that of the three-factor MSKCC model. DF/HCC Kidney Cancer SPORE P50 CA101942-01, Kidney Cancer Research Network of Canada, Canadian Institute for Health Research, Trust Family, Loker Pinard, Michael Brigham, and Gerald DeWulf.

MeSH Terms
Asia Canada Carcinoma, Renal Cell/drug therapy,mortality,secondary Chi-Square Distribution Databases, Factual Decision Support Techniques Europe Female Humans Kaplan-Meier Estimate Kidney Neoplasms/drug therapy,mortality,pathology Male Middle Aged Molecular Targeted Therapy/adverse effects,mortality Multivariate Analysis Patient Selection Predictive Value of Tests Proportional Hazards Models Retrospective Studies Risk Assessment Risk Factors Salvage Therapy/adverse effects,mortality Time Factors Treatment Outcome United States
Authors & Affiliations
20 authors, click to expand affiliations / ORCID
Ko Jenny J
Department of Medical Oncology, Tom Baker Cancer Centre, University of Calgary, Calgary, AB, Canada.
Xie Wanling
Dana-Farber Cancer Institute, Boston, MA, USA.
Kroeger Nils
Department of Urology, University Hospital Greifswald, Ernst Moritz Arndt University, Greifswald, Germany.
Lee Jae-Lyun
Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
Rini Brian I
Cleveland Clinic, Taussig Cancer Institute, Cleveland, OH, USA.
Knox Jennifer J
Department of Medical Oncology, Princess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada.
Bjarnason Georg A
Sunnybrook Odette Cancer Centre, University of Toronto, Toronto, ON, Canada.
Srinivas Sandy
Division of Oncology, Stanford Medical Center, Stanford, CA, USA.
Pal Sumanta K
City of Hope Comprehensive Cancer Center, Medical Oncology & Experimental Therapeutics, Duarte, CA, USA.
Yuasa Takeshi
Department of Urology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Smoragiewicz Martin
Department of Medical Oncology, British Columbia Cancer Agency, University of British Columbia, Vancouver, BC, Canada.
Donskov Frede
Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Kanesvaran Ravindran
Division of Medical Oncology, National Cancer Centre Singapore, Singapore.
Wood Lori
Queen Elizabeth II Health Sciences Centre, Dalhousie University, Halifax, NS, Canada.
Ernst D Scott
London Regional Cancer Centre, London, ON, Canada.
Agarwal Neeraj
University of Utah Huntsman Cancer Institute, Salt Lake City, UT, USA.
Vaishampayan Ulka N
Karmanos Cancer Institute, Wayne State University, Detroit, MI, USA.
Rha Sun-Young
Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea.
Choueiri Toni K
Dana-Farber Cancer Institute, Boston, MA, USA.
Heng Daniel Y C
Department of Medical Oncology, Tom Baker Cancer Centre, University of Calgary, Calgary, AB, Canada. Electronic address: daniel.heng@albertahealthservices.ca.
Article Info
Journal
The Lancet. Oncology
Abbr.
Lancet Oncol
ISSN
1474-5488
Published
2015-03-00
Epub
2015-00-12
Pages
293-300
Language
English
Region
England
NLM ID
100957246
Subset
IM
Grants
NCI NIH HHS · P50 CA101942-01 · United States
Canadian Institutes of Health Research · Canada
Corrections
CommentIn
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