Predictive role of plasma vascular endothelial growth factor for the effect of celecoxib in advanced non-small cell lung cancer treated with chemotherapy

被引:21
作者
Sorenson, Sverre [1 ,2 ]
Fohlin, Helena [3 ]
Lindgren, Andrea [4 ]
Lindskog, Magnus [5 ,6 ]
Bergman, Bengt [7 ,8 ]
Sederholm, Christer [2 ]
Ek, Lars [9 ]
Lamberg, Kristina [10 ]
Clinchy, Birgitta [11 ]
机构
[1] Linkoping Univ, Fac Hlth Sci, Dept Med & Hlth Sci, S-58183 Linkoping, Sweden
[2] Cty Council Ostergotland, Dept Pulm Med UHL, Linkoping, Sweden
[3] Cty Council Ostergotland, Reg Canc Ctr, Linkoping, Sweden
[4] Cty Council Ostergotland, Allergy Ctr UHL, Linkoping, Sweden
[5] Uppsala Univ, Dept Radiol Oncol & Radiat Sci, Uppsala, Sweden
[6] Uppsala Univ, Dept Med Sci, Uppsala, Sweden
[7] Sahlgrens Univ Hosp, Dept Resp Med, Gothenburg, Sweden
[8] Univ Gothenburg, Inst Med, Gothenburg, Sweden
[9] Skane Univ Hosp, Dept Resp Med & Allergol, Lund, Sweden
[10] Univ Uppsala Hosp, Dept Pulm Med, Uppsala, Sweden
[11] Linkoping Univ, Fac Hlth Sci, Dept Clin & Expt Med, Div Clin Immunol, S-58183 Linkoping, Sweden
[12] Cty Council Ostergotland, Dept Clin Immunol & Transfus Med, Linkoping, Sweden
基金
英国医学研究理事会;
关键词
Non-small cell lung cancer; Celecoxib; Chemotherapy; Survival; Plasma VEGF; FACTOR VEGF; PHASE-III; INHIBITION; EXPRESSION; APOPTOSIS; BLOOD;
D O I
10.1016/j.ejca.2012.07.032
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim of the study: The primary purpose of this study is to investigate if pretreatment plasma levels of vascular endothelial growth factor (VEGF) are predictive of the effect of celecoxib on survival in advanced non-small cell lung cancer (NSCLC) treated with palliative chemotherapy. A secondary objective is to describe the course of plasma VEGF levels during and after treatment with cytotoxic chemotherapy combined with celecoxib or placebo. Methods: In a previously published double-blind multicenter phase III trial, 316 patients with NSCLC stage IIIB or IV and World Health Organisation (WHO) performance status 0-2 were randomised to receive celecoxib 400 mg b.i.d. or placebo in combination with two-drug platinum-based chemotherapy. Chemotherapy cycle length was three weeks and planned duration of chemotherapy was four cycles. Celecoxib was given for a maximum of one year but was stopped earlier in case of disease progression or prohibitive toxicity. In a subset of patients, plasma VEGF levels were examined at onset of treatment and at 6, 12 and 20 weeks. Results: VEGF levels at start of treatment were obtained in 107 patients at four study sites. The median value was 70 pg/ml. Mean values declined during the first 12 weeks and then increased at 20 weeks. A subpopulation treatment effect pattern plot (STEPP) analysis showed an inverse relationship between initial plasma VEGF and the impact of celecoxib on survival with zero effect at 200 pg/ml. The effect on survival by celecoxib in the whole subset of patients was positive (hazard ratio (HR)=0.64 [confidence interval (CI) 0.43-0.95], p=0.028). Conclusion: Low pretreatment plasma levels of VEGF appear to be predictive of a positive effect of celecoxib on survival. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:115 / 120
页数:6
相关论文
共 21 条
[1]  
Bonetti M, 2000, STAT MED, V19, P2595, DOI 10.1002/1097-0258(20001015)19:19<2595::AID-SIM562>3.0.CO
[2]  
2-M
[3]   Cyclooxygenase as a target in lung cancer [J].
Brown, JR ;
DuBois, RN .
CLINICAL CANCER RESEARCH, 2004, 10 (12) :4266S-4269S
[4]   Reclinical evaluation of the nonsteroidal anti-inflammatory agent celecoxib on malignant mesothelioma chemoprevention [J].
Catalano, A ;
Graciotti, L ;
Rinaldi, L ;
Raffaelli, G ;
Rodilosso, S ;
Betta, P ;
Gianni, W ;
Amoroso, S ;
Procopio, A .
INTERNATIONAL JOURNAL OF CANCER, 2004, 109 (03) :322-328
[5]   Inhibition of cyclo-oxygenase 2 reduces tumor metastasis and inflammatory signaling during blockade of vascular endothelial growth factor [J].
Fisher, Jason C. ;
Gander, Jeffrey W. ;
Haley, Mary Jo ;
Hernandez, Sonia L. ;
Huang, Jianzhong ;
Chang, Yan-Jung ;
Johung, Tessa B. ;
Guarnieri, Paolo ;
O'Toole, Kathleen ;
Yamashiro, Darrell J. ;
Kandel, Jessica J. .
VASCULAR CELL, 2011, 3
[6]   Randomized, Placebo-Controlled Phase III Study of Docetaxel Plus Carboplatin With Celecoxib and Cyclooxygenase-2 Expression As a Biomarker for Patients With Advanced Non-Small-Cell Lung Cancer: The NVALT-4 Study [J].
Groen, Harry J. M. ;
Sietsma, Hannie ;
Vincent, Andrew ;
Hochstenbag, Monique M. H. ;
van Putten, John W. G. ;
van den Berg, Anke ;
Dalesio, Otilia ;
Biesma, Bonne ;
Smit, Hans J. M. ;
Termeer, Arien ;
Hiltermann, T. Jeroen N. ;
van den Borne, Ben E. E. M. ;
Schramel, Franz M. N. H. .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (32) :4320-4326
[7]   Baseline Vascular Endothelial Growth Factor Concentration as a Potential Predictive Marker of Benefit from Vandetanib in Non-Small Cell Lung Cancer [J].
Hanrahan, Emer O. ;
Ryan, Anderson J. ;
Mann, Helen ;
Kennedy, Sarah J. ;
Langmuir, Peter ;
Natale, Ronald B. ;
Herbst, Roy S. ;
Johnson, Bruce E. ;
Heymach, John V. .
CLINICAL CANCER RESEARCH, 2009, 15 (10) :3600-3609
[8]   A critical review of vascular endothelial growth factor (VEGF) analysis in peripheral blood: Is the current literature meaningful? [J].
Hormbrey, E ;
Gillespie, P ;
Turner, K ;
Han, C ;
Roberts, A ;
McGrouther, D ;
Harris, AL .
CLINICAL & EXPERIMENTAL METASTASIS, 2002, 19 (08) :651-663
[9]   Combined VEGF-A and VEGFR-2 concentrations in plasma: Diagnostic and prognostic implications in patients with advanced NSCLC [J].
Jantus-Lewintre, Eloisa ;
Sanmartin, Elena ;
Sirera, Rafael ;
Blasco, Ana ;
Javier Sanchez, Jose ;
Taron, Miguel ;
Rosell, Rafael ;
Camps, Carlos .
LUNG CANCER, 2011, 74 (02) :326-331
[10]  
Jelkmann W, 2001, CLIN CHEM, V47, P617