Baseline Vascular Endothelial Growth Factor Concentration as a Potential Predictive Marker of Benefit from Vandetanib in Non-Small Cell Lung Cancer

被引:82
作者
Hanrahan, Emer O.
Ryan, Anderson J. [2 ]
Mann, Helen [2 ]
Kennedy, Sarah J. [2 ]
Langmuir, Peter [3 ]
Natale, Ronald B. [4 ]
Herbst, Roy S.
Johnson, Bruce E. [5 ]
Heymach, John V. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol & Canc Biol, Unit 432, Houston, TX 77030 USA
[2] AstraZeneca, Macclesfield, Cheshire, England
[3] AstraZeneca, Wilmington, DE USA
[4] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
[5] Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
TYROSINE KINASE INHIBITORS; PHASE-III TRIAL; FACTOR RECEPTOR; TUMOR ANGIOGENESIS; PLUS BEVACIZUMAB; PACLITAXEL; VEGF; CARBOPLATIN; CHEMOTHERAPY; COMBINATION;
D O I
10.1158/1078-0432.CCR-08-2568
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Vandetanib [vascular endothelial growth factor (VEGF) receptor/epidermal growth factor receptor/RET inhibitor] has shown improvements in progression-free survival (PFS) in advanced non-small cell lung cancer in three randomized phase II studies: vandetanib versus gefitinib (study 3), docetaxel vandetanib (study 6), and carboplatin-paclitaxel and/or vandetanib (study 7). In study 7, vandetanib monotherapy was inferior to carboplatin-paclitaxel. We performed an exploratory retrospective analysis of the relationship between baseline circulating VEGF concentrations and PFS. Experimental Design: Mean baseline VEGF levels were determined by ELISA from two baseline samples of plasma (163 of 168 patients, study 3; 65 of 127, study 6) or serum (144 of 181, study 7). High baseline VEGF values were above the immunoassay reference range for healthy subjects; low baseline VEGF values were within the range. Results: Patients with low baseline VEGF had a lower risk of disease progression with vandetanib versus gefitinib [hazard ratio (HR), 0.55; 95% confidence interval (95% CI), 0.35-0.86; P = 0.01] or vandetanib 100 mg/d + docetaxel versus docetaxel (HR, 0.25; 95% CI, 0.09-0.68; P = 0.01). High VEGF patients had a similar risk of disease progression with vandetanib monotherapy versus gefitinib (HR, 1.03; 95% CI, 0.60-1.75; P = 0.92) or vandetanib 100 mg/d + docetaxel versus docetaxel (HR, 0.95; 95% CI, 0.25-3.61; P = 0.94). In study 7, low VEGF patients had a similar risk of disease progression with vandetanib monotherapy 300 mg/d versus carboplatin-paclitaxel (HR, 0.80; 95% CI, 0.41-1.56; P = 0.51); high VEGF patients progressed more quickly (HR, 1.60; 95% CI, 0.81-3.15; P = 0.17). Conclusions: These analyses suggest that low baseline circulating VEGF may be predictive of PFS advantage in patients with advanced non-small cell lung cancer receiving vandetanib versus gefitinib or vandetanib + docetaxel versus docetaxel. Moreover, patients with low VEGF levels may have a similar outcome with either vandetanib monotherapy or carboplatin-paclitaxel.
引用
收藏
页码:3600 / 3609
页数:10
相关论文
共 42 条
[1]   Nuclear factor-κB-related serum factors as longitudinal biomarkers of response and survival in advanced oropharyngeal carcinoma [J].
Allen, Clint ;
Duffy, Sonia ;
Teknos, Theodoros ;
Islam, Mozaffarul ;
Chen, Zhong ;
Albert, Paul S. ;
Wolf, Gregory ;
Van Wales, Carter .
CLINICAL CANCER RESEARCH, 2007, 13 (11) :3182-3190
[2]   Increased plasma vascular endothelial growth factor (VEGF) as a surrogate marker for optimal therapeutic dosing of VEGF receptor-2 monoclonal antibodies [J].
Bocci, G ;
Man, S ;
Green, SK ;
Francia, G ;
Ebos, JML ;
du Manoir, JM ;
Weinerman, A ;
Emmenegger, U ;
Ma, L ;
Thorpe, P ;
Davidoff, A ;
Huber, J ;
Hicklin, DJ ;
Kerbel, RS .
CANCER RESEARCH, 2004, 64 (18) :6616-6625
[3]   Angiogenesis in non-small cell lung cancer: The prognostic impact of neoangiogenesis and the cytokines VEGF and bFGF in tumours and blood [J].
Bremnes, RM ;
Camps, C ;
Sirera, R .
LUNG CANCER, 2006, 51 (02) :143-158
[4]  
Bukowski RM, 2007, J CLIN ONCOL, V25, DOI 10.1200/JCO.2007.11.5154
[5]   VEGF as a Marker for Outcome Among Advanced Breast Cancer Patients Receiving anti-VEGF Therapy with Bevacizumab and Vinorelbine Chemotherapy [J].
Burstein, Harold J. ;
Chen, Yu-Hui ;
Parker, Leroy M. ;
Savoie, Jennifer ;
Younger, Jerry ;
Kuter, Irene ;
Ryan, Paula D. ;
Garber, Judy E. ;
Chen, Helen ;
Campos, Susana M. ;
Shulman, Lawrence N. ;
Harris, Lyndsay N. ;
Gelman, Rebecca ;
Winer, Eric P. .
CLINICAL CANCER RESEARCH, 2008, 14 (23) :7871-7877
[6]   Pharmacodynamic separation of epidermal growth factor receptor tyrosine kinase inhibitors and chemotherapy in non-small-cell lung cancer [J].
Davies, Angela M. ;
Ho, Cheryl ;
Lara, Primo N., Jr. ;
Mack, Philip ;
Gumerlock, Paul H. ;
Gandara, David R. .
CLINICAL LUNG CANCER, 2006, 7 (06) :385-388
[7]   Cell adhesion molecules, vascular endothelial growth factor, and basic fibroblast growth factor in patients with non-small cell lung cancer treated with chemotherapy with or without bevacizumab - an eastern cooperative oncology group study [J].
Dowlati, Afshin ;
Gray, Robert ;
Sandler, Alan B. ;
Schiller, Joan H. ;
Johnson, David H. .
CLINICAL CANCER RESEARCH, 2008, 14 (05) :1407-1412
[8]   Soluble markers for the assessment of biological activity with PTK787/ZK 222584 (PTK/ZK), a vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitor in patients with advanced colorectal cancer from two phase I trials [J].
Drevs, J ;
Zirrgiebel, U ;
Schmidt-Gersbach, CIM ;
Mross, K ;
Medinger, M ;
Lee, L ;
Pinheiro, J ;
Wood, J ;
Thomas, AL ;
Unger, C ;
Henry, A ;
Steward, WP ;
Laurent, D ;
Lebwohl, D ;
Dugan, M ;
Marmé, D .
ANNALS OF ONCOLOGY, 2005, 16 (04) :558-565
[9]   Vascular permeability factor/vascular endothelial growth factor: A critical cytokine in tumor angiogenesis and a potential target for diagnosis and therapy [J].
Dvorak, HF .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (21) :4368-4380
[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