Biomarkers Predicting Outcome in Patients with Advanced Renal Cell Carcinoma: Results from Sorafenib Phase III Treatment Approaches in Renal Cancer Global Evaluation Trial

被引:136
作者
Pena, Carol [1 ]
Lathia, Chetan [1 ]
Shan, Minghua [1 ]
Escudier, Bernard [2 ]
Bukowski, Ronald M. [3 ]
机构
[1] Bayer HealthCare Pharmaceut Inc, Montville, NJ 07045 USA
[2] Inst Gustave Roussy, Villejuif, France
[3] Cleveland Clin Taussig Canc Ctr, Cleveland, OH USA
关键词
ENDOTHELIAL GROWTH-FACTOR; CARBONIC-ANHYDRASE-IX; PLASMA TISSUE INHIBITOR; FACTOR-TARGETED THERAPY; LONG-TERM SURVIVAL; INDEPENDENT PREDICTOR; ANTITUMOR-ACTIVITY; TUMOR PROGRESSION; SUNITINIB MALATE; METALLOPROTEINASE-1;
D O I
10.1158/1078-0432.CCR-09-3343
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Plasma proteins [vascular endothelial growth factor (VEGF), soluble VEGF receptor 2 (sVEGFR-2), carbonic anhydrase IX (CAIX), tissue inhibitor of metalloproteinase 1 (TIMP-1), and Ras p21] and one tumor gene (VHL) were analyzed to identify prognostic biomarkers or indicators of response to sorafenib in a subset of patients enrolled in the Treatment Approaches in Renal Cancer Global Evaluation Trial. Experimental Design: Nine hundred three patients with advanced renal cell carcinoma (RCC) were randomized to 400 mg sorafenib twice a day or placebo. Samples collected at baseline and after 3 and 12 weeks were subjected to enzyme-linked immunosorbent assays. VHL exons were sequenced from tumor biopsies. Results: Baseline biomarker data were available for VEGF (n = 712), sVEGFR-2 (n = 713), CAIX (n = 128), TIMP-1 (n = 123), Ras p21 (n = 125), and VHL mutational status (n = 134). Higher Eastern Cooperative Oncology Group performance status (ECOG PS) score correlated with elevated baseline VEGF (P < 0.0001) and a higher incidence of VHL mutations (P = 0.008), whereas higher Memorial Sloan-Kettering Cancer Center (MSKCC) score correlated with elevated VEGF (P < 0.0001), CAIX (P = 0.027), and TIMP-1 (P = 0.0001). Univariable analyses of baseline levels in the placebo cohort identified VEGF (P = 0.0024), CAIX (P = 0.034), TIMP-1 (P = 0.001), and Ras p21 (P = 0.016) as prognostic biomarkers for survival. TIMP-1 remained prognostic for survival in a multivariable analysis model (P = 0.002) that also included ECOG PS, MSKCC score, and the other biomarkers assayed. In the placebo cohort, TIMP-1 (P < 0.001) and Ras p21 (P = 0.048) levels increased at 12 weeks. In the sorafenib cohort, VEGF levels increased at 3 and 12 weeks of treatment (both weeks P < 0.0001), whereas sVEGFR-2 (both weeks P < 0.0001) and TIMP-1 levels (P = 0.002, week 3; P = 0.006, week 12) decreased. Conclusions: VEGF, CAIX, TIMP-1, and Ras p21 levels were prognostic for survival in RCC patients. Of these, TIMP-1 has emerged as being independently prognostic. Clin Cancer Res; 16(19); 4853-63. (C) 2010 AACR.
引用
收藏
页码:4853 / 4863
页数:11
相关论文
共 46 条
[1]   Raf: A strategic target for therapeutic development against cancer [J].
Beeram, M ;
Patnaik, A ;
Rowinsky, EK .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (27) :6771-6790
[2]  
Bhuvarahamurthy V, 2006, ONCOL REP, V15, P1379
[3]  
Bui MHT, 2003, CLIN CANCER RES, V9, P802
[4]  
BUKOWSKI R, 2009, CANCER, V15, P2273
[5]   Phase II study of sunitinib malate, an oral multitargeted tyrosine kinase inhibitor, in patients with metastatic breast cancer previously treated with an anthracycline and a taxane [J].
Burstein, Harold J. ;
Elias, Anthony D. ;
Rugo, Hope S. ;
Cobleigh, Melody A. ;
Wolff, Antonio C. ;
Eisenberg, Peter D. ;
Lehman, Mary ;
Adams, Bonne J. ;
Bello, Carlo L. ;
DePrimo, Samuel E. ;
Baum, Charles M. ;
Miller, Kathy D. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (11) :1810-1816
[6]   Increasing complexity of Ras signaling [J].
Campbell, SL ;
Khosravi-Far, R ;
Rossman, KL ;
Clark, GJ ;
Der, CJ .
ONCOGENE, 1998, 17 (11) :1395-1413
[7]   BAY 43-9006 inhibition of oncogenic RET mutants [J].
Carlomagno, F ;
Anaganti, S ;
Guida, T ;
Salvatore, G ;
Troncone, G ;
Wilhelm, SM ;
Santoro, M .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (05) :326-334
[8]   Hypoxia-Inducible Carbonic Anhydrase IX and XII Promote Tumor Cell Growth by Counteracting Acidosis through the Regulation of the Intracellular pH [J].
Chiche, Johanna ;
Ilc, Karine ;
Laferriere, Julie ;
Trottier, Eric ;
Dayan, Frederic ;
Mazure, Nathalie M. ;
Brahimi-Horn, M. Christiane ;
Pouyssegur, Jacques .
CANCER RESEARCH, 2009, 69 (01) :358-368
[9]   Circulating protein biomarkers of pharmacodynamic activity of sunitinib in patients with metastatic renal cell carcinoma: modulation of VEGF and VEGF-related proteins [J].
DePrimo, Samuel E. ;
Bello, Carlo L. ;
Smeraglia, John ;
Baum, Charles M. ;
Spinella, Dominic ;
Rini, Brian I. ;
Michaelson, M. Dror ;
Motzer, Robert J. .
JOURNAL OF TRANSLATIONAL MEDICINE, 2007, 5
[10]   Multiple circulating proangiogenic factors induced by sunitinib malate are tumor-independent and correlate with antitumor efficacy [J].
Ebos, John M. L. ;
Lee, Christina R. ;
Christensen, James G. ;
Mutsaers, Anthony J. ;
Kerbel, Robert S. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (43) :17069-17074