Bevacizumab and oxaliplatin-based chemotherapy in metastatic colorectal cancer

被引:12
作者
Beatty, Gregory L.
Giantonio, Bruce J.
机构
[1] Hospital of the University of Pennsylvania, Division of Hematology/Oncology, Philadelphia, PA 19104
[2] Philadelphia, PA 19104, 12 Penn Tower
关键词
advanced colorectal cancer; angiogenesis; bevacizumab; chemotherapy; metastatic; oxaliplatin; vascular endothelial growth factor; VEGF;
D O I
10.1586/14737140.8.5.683
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
In metastatic colorectal cancer disease progression correlates with serum VEGF levels. The importance of VEGF in tumor-induced angiogenesis is well described in preclinical models. In this review we discuss the role of anti-VEGF therapy in combination with oxaliplatin-based chemotherapy for the treatment of metastatic colorectal cancer. A recent Phase III clinical trial in patients with metastatic colorectal cancer demonstrated the efficacy of FOLFOX4 in combination with bevacizumab, a recombinant humanized monoclonal antibody with high binding specificity for VEGF, to improve median overall survival when used as second-line therapy. The major adverse events associated with bevacizumab include grade III hypertension, bleeding and the risk of gastrointestinal perforation. Combining bevacizumab with oxaliplatin-based chemotherapy as first-line treatment for patients with metastatic colorectal cancer improves progression-free survival, as seen in the NO16966 and Panitumumab Advanced Colorectal Cancer Evaluation (PACCE) studies, when compared with placebo and historical controls, respectively Future research will need to focus on the mechanisms whereby bevacizumab enhances the benefit of chemotherapy to identify predictive markers that better define which patient populations will benefit the most from treatment.
引用
收藏
页码:683 / 688
页数:6
相关论文
共 46 条
[1]
EXPRESSION OF THE VASCULAR-PERMEABILITY FACTOR VASCULAR ENDOTHELIAL GROWTH-FACTOR GENE IN CENTRAL-NERVOUS-SYSTEM NEOPLASMS [J].
BERKMAN, RA ;
MERRILL, MJ ;
REINHOLD, WC ;
MONACCI, WT ;
SAXENA, A ;
CLARK, WC ;
ROBERTSON, JT ;
ALI, IU ;
OLDFIELD, EH .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (01) :153-159
[2]
Borgström P, 1999, ANTICANCER RES, V19, P4203
[3]
BROWN LF, 1993, CANCER RES, V53, P4727
[4]
Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[5]
Leucovorin and fluorouracil with or without oxaliplatin as first-line treatment in advanced colorectal cancer [J].
de Gramont, A ;
Figer, A ;
Seymour, M ;
Homerin, M ;
Hmissi, A ;
Cassidy, J ;
Boni, C ;
Cortes-Funes, H ;
Cervantes, A ;
Freyer, G ;
Papamichael, D ;
Le Bail, N ;
Louvet, C ;
Hendler, D ;
de Braud, F ;
Wilson, C ;
Morvan, F ;
Bonetti, A .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (16) :2938-2947
[6]
DeVore R, 2000, P AM SOC CLIN ONCOL, V19
[7]
Revacizumab-induced transient remodeling of the vasculature in neuroblastoma xenografts results in improved delivery and efficacy of systemically administered chemotherapy [J].
Dickson, Paxton V. ;
Hamner, John B. ;
Sims, Thomas L. ;
Fraga, Charles H. ;
Ng, Catherine Y. C. ;
Rajasekeran, Surender ;
Hagedorn, Nikolaus L. ;
McCarville, M. Beth ;
Stewart, Clinton F. ;
Davidoff, Andrew M. .
CLINICAL CANCER RESEARCH, 2007, 13 (13) :3942-3950
[8]
Dirix LY, 1996, ANN ONCOL, V7, P843
[10]
DVORAK HF, 1995, AM J PATHOL, V146, P1029