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
[21]   Gefitinib in combination with paclitaxel and carboplatin in advanced non-small-cell lung cancer: A phase III trial - INTACT 2 [J].
Herbst, RS ;
Giaccone, G ;
Schiller, JH ;
Natale, RB ;
Miller, V .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (05) :785-794
[22]   TRIBUTE: A phase III trial of erlotinib hydrochloride (OSI-774) combined with carboplatin and paclitaxel chemotherapy in advanced non-small-cell lung cancer [J].
Herbst, RS ;
Prager, D ;
Hermann, R ;
Fehrenbacher, L ;
Johnson, BE ;
Sandler, A ;
Kris, MG ;
Tran, HT ;
Klein, P ;
Li, X ;
Ramies, D ;
Johnson, DH ;
Miller, VA .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :5892-5899
[23]   Randomized, placebo-controlled phase II study of vandetanib plus docetaxel in previously treated non-small-cell lung cancer [J].
Heymach, John V. ;
Johnson, Bruce E. ;
Prager, Diane ;
Csada, Edit ;
Roubec, Jaromir ;
Pesek, Milos ;
Spasova, Irena ;
Belani, Chandra P. ;
Bodrogi, Istvan ;
Gadgeel, Shirish ;
Kennedy, Sarah J. ;
Hou, Jeannie ;
Herbst, Roy S. .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (27) :4270-4277
[24]   Randomized Phase II Study of Vandetanib Alone or With Paclitaxel and Carboplatin as First-Line Treatment for Advanced Non-Small-Cell Lung Cancer [J].
Heymach, John V. ;
Paz-Ares, Luis ;
De Braud, Filippo ;
Sebastian, Martin ;
Stewart, David J. ;
Eberhardt, Wilfried E. E. ;
Ranade, Anantbhushan A. ;
Cohen, Graham ;
Trigo, Jose Manuel ;
Sandler, Alan B. ;
Bonomi, Philip D. ;
Herbst, Roy S. ;
Krebs, Annetta D. ;
Vasselli, James ;
Johnson, Bruce E. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (33) :5407-5415
[25]   Role of the vascular endothelial growth factor pathway in tumor growth and angiogenesis [J].
Hicklin, DJ ;
Ellis, LM .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (05) :1011-1027
[26]  
Holden S.N., 2005, J CLIN ONCOL, V23, P3555
[27]   Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer [J].
Hurwitz, H ;
Fehrenbacher, L ;
Novotny, W ;
Cartwright, T ;
Hainsworth, J ;
Heim, W ;
Berlin, J ;
Baron, A ;
Griffing, S ;
Holmgren, E ;
Ferrara, N ;
Fyfe, G ;
Rogers, B ;
Ross, R ;
Kabbinavar, F .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (23) :2335-2342
[28]   Vascular endothelial growth factor expression in non-small-cell lung cancer: Prognostic significance in squamous cell carcinoma [J].
Imoto, H ;
Osaki, T ;
Taga, S ;
Ohgami, A ;
Ichiyoshi, Y ;
Yasumoto, K .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1998, 115 (05) :1007-1014
[29]  
Karrison T, 2007, J CLIN ONCOL, V25
[30]   A randomized, bouble-blind, phase IIa dose-finding study of Vandetanib (ZD6474) in Japanese patients with nonsmall cell lung cancer [J].
Kiura, Katsuyuki ;
Nakagawa, Kazuhiko ;
Shinkai, Tetsu ;
Eguchi, Kenji ;
Ohe, Yuichiro ;
Yamamoto, Nobuyuki ;
Tsuboi, Masahiro ;
Yokota, Soichiro ;
Seto, Takashi ;
Jiang, Haiyi ;
Nishio, Kazuto ;
Saijo, Nagahiro ;
Fukuoka, Masahiro .
JOURNAL OF THORACIC ONCOLOGY, 2008, 3 (04) :386-393