Evaluating antiangiogenesis agents in the clinic: The Eastern Cooperative Oncology Group portfolio of clinical trials

被引:37
作者
Sparano, JA [1 ]
Gray, R [1 ]
Giantonio, B [1 ]
O'Dwyer, P [1 ]
Comis, RL [1 ]
机构
[1] Eastern Cooperat Oncol Grp, Philadelphia, PA USA
关键词
D O I
10.1158/1078-0432.CCR-03-0238
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent evidence indicates that treatment with a humanized monoclonal antibody (bevacizumab) directed at vascular endothelial growth factor improves response and survival in metastatic colorectal cancer when added to standard chemotherapy, validating angiogenesis as a therapeutic target. Investigators from the Eastern Cooperative Oncology Group (ECOG) have initiated a number of Phase III studies that will help further define the role of antiangiogenic agents for the treatment of breast, colon, lung, renal, and head and neck cancer, as well as melanoma and myeloma. The agents being evaluated target various biological functions involved in angiogenesis, including vascular endothelial growth factor (bevacizumab), endothelial cell proliferation (thalidomide, IFN-alpha), and matrix metalloproteinases (marimastat). These clinical trials include correlative laboratory studies aimed at elucidating how these agents may exert their clinical effects. The portfolio of Eastern Cooperative Oncology Group studies will serve to further define the role of this therapeutic strategy for patients with advanced cancer.
引用
收藏
页码:1206 / 1211
页数:6
相关论文
共 54 条
[1]   Extended survival in advanced and refractory multiple myeloma after single-agent thalidomide: identification of prognostic factors in a phase 2 study of 169 patients [J].
Barlogie, B ;
Desikan, R ;
Eddlemon, P ;
Spencer, T ;
Zeldis, J ;
Munshi, N ;
Badros, A ;
Zangari, M ;
Anaissie, E ;
Epstein, J ;
Shaughnessy, J ;
Ayers, D ;
Spoon, D ;
Tricot, G .
BLOOD, 2001, 98 (02) :492-494
[2]   IFN-α2b and thalidomide synergistically inhibit tumor-induced angiogenesis [J].
Bauer, JA ;
Morrison, BH ;
Grane, RW ;
Jacobs, BS ;
Borden, EC ;
Lindner, DJ .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2003, 23 (01) :3-10
[3]   Aberrant methylation of p16INK4a is an early event in lung cancer and a potential biomarker for early diagnosis [J].
Belinsky, SA ;
Nikula, KJ ;
Palmisano, WA ;
Michels, R ;
Saccomanno, G ;
Gabrielson, E ;
Baylin, SB ;
Herman, JG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (20) :11891-11896
[4]  
BENSON AB, 2003, P AN M AM SOC CLIN, V22, P243
[5]   Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis [J].
Bergers, G ;
Brekken, R ;
McMahon, G ;
Vu, TH ;
Itoh, T ;
Tamaki, K ;
Tanzawa, K ;
Thorpe, P ;
Itohara, S ;
Werb, Z ;
Hanahan, D .
NATURE CELL BIOLOGY, 2000, 2 (10) :737-744
[6]  
BISSETT D, 2002, P AN M AM SOC CLIN, V21, pA296
[7]   Marimastat as maintenance therapy for patients with advanced gastric cancer: a randomised trial [J].
Bramhall, SR ;
Hallissey, MT ;
Whiting, J ;
Scholefield, J ;
Tierney, G ;
Stuart, RC ;
Hawkins, RE ;
McCulloch, P ;
Maughan, T ;
Brown, PD ;
Baillet, M .
BRITISH JOURNAL OF CANCER, 2002, 86 (12) :1864-1870
[8]   A double-blind placebo-controlled, randomised study comparing gemcitabine and marimastat with gemcitabine and placebo as first line therapy in patients with advanced pancreatic cancer [J].
Bramhall, SR ;
Schulz, J ;
Nemunaitis, J ;
Brown, PD ;
Baillet, M ;
Buckels, JAC .
BRITISH JOURNAL OF CANCER, 2002, 87 (02) :161-167
[9]   Marimastat as first-line therapy for patients with unresectable pancreatic cancer: A randomized trial [J].
Bramhall, SR ;
Rosemurgy, A ;
Brown, PD ;
Bowry, C ;
Buckels, JAC .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (15) :3447-3455
[10]   Clinical studies with matrix metalloproteinase inhibitors [J].
Brown, PD .
APMIS, 1999, 107 (01) :174-180