Expanding the clinical development of bevacizumab

被引:30
作者
Chen, HX [1 ]
机构
[1] NCI, Canc Therapy Evaluat Program, Bethesda, MD 20892 USA
关键词
vascular endothelial growth factor; clinical trial; cancer; monoclonal antibody; bevacizumab;
D O I
10.1634/theoncologist.9-suppl_1-27
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Bevacizutnab (Avastin(TM); Genentech, Inc.; South San Francisco, CA) is a recombinant, humanized monoclonal antibody to vascular endothelial growth factor, a key regulator of tumor angiogenesis. Bevacizumab demonstrated potent antitumor activity in preclinical models and has also shown biologic activity and clinical benefit in clinical studies. Notably, a randomized, placebo-controlled phase II trial in renal cell carcinoma demonstrated a significantly longer time to tumor progression with bevacizumab monotherapy. Furthermore, in a phase III trial for untreated advanced colorectal cancer, the addition of bevacizumab to chemotherapy led to significantly longer overall survival and progression-free survival times than chemotherapy alone. The clinical development of bevacizurnab has been expanded to include confirmatory phase III trials and exploratory phase II trials in a variety of solid tumors and hematologic malignancies. Treatment regimens being examined include bevacizumab alone and in combination with conventional chemotherapy, radiation, immune therapy, and biologically targeted agents.
引用
收藏
页码:27 / 35
页数:9
相关论文
共 81 条
[1]   Angiogenesis in acute and chronic leukemias and myelodysplastic syndromes [J].
Aguayo, A ;
Kantarjian, H ;
Manshouri, T ;
Gidel, C ;
Estey, E ;
Thomas, D ;
Koller, C ;
Estrov, Z ;
O'Brien, S ;
Keating, M ;
Freireich, E ;
Albitar, M .
BLOOD, 2000, 96 (06) :2240-2245
[2]   Cellular vascular endothelial growth factor is a predictor of outcome in patients with acute myeloid leukemia [J].
Aguayo, A ;
Estey, E ;
Kantarjian, H ;
Mansouri, T ;
Gidel, C ;
Keating, M ;
Giles, F ;
Estrov, Z ;
Barlogie, B ;
Albitar, M .
BLOOD, 1999, 94 (11) :3717-3721
[3]   Evidence for mRNA expression of vascular endothelial growth factor by X-ray irradiation in a lung squamous carcinoma cell line [J].
Ando, S ;
Nojima, K ;
Majima, H ;
Ishihara, H ;
Suzuki, M ;
Furusawa, Y ;
Yamaguchi, H ;
Koike, S ;
Ando, K ;
Yamauchi, M ;
Kuriyama, T .
CANCER LETTERS, 1998, 132 (1-2) :75-80
[4]  
Arii S, 1999, Hum Cell, V12, P25
[5]  
Bellamy WT, 1999, CANCER RES, V59, P728
[6]   Vascular endothelial cell growth factor is an autocrine promoter of abnormal localized immature myeloid precursors and leukemia progenitor formation in myelodysplastic syndromes [J].
Bellamy, WT ;
Richter, L ;
Sirjani, D ;
Roxas, C ;
Glinsmann-Gibson, B ;
Frutiger, Y ;
Grogan, TM ;
List, AF .
BLOOD, 2001, 97 (05) :1427-1434
[7]   BONE-MARROW CONNECTIVE-TISSUE AND THE HEMATOPOIETIC MICRO-ENVIRONMENT [J].
BENTLEY, SA .
BRITISH JOURNAL OF HAEMATOLOGY, 1982, 50 (01) :1-6
[8]   Maximizing the potential of bevacizumab in cancer treatment [J].
Bergsland, E ;
Dickler, MN .
ONCOLOGIST, 2004, 9 :36-42
[9]   VEGF-RII influences the prognosis of pancreatic cancer [J].
Büchler, P ;
Reber, HA ;
Büchler, MW ;
Friess, H ;
Hines, OJ .
ANNALS OF SURGERY, 2002, 236 (06) :738-749
[10]   Vascular endothelial growth factor and interleukin-6 in paracrine tumor-stromal cell interactions in multiple myeloma [J].
Dankbar, B ;
Padró, T ;
Leo, R ;
Feldmann, B ;
Kropff, M ;
Mesters, RM ;
Serve, H ;
Berdel, WE ;
Kienast, J .
BLOOD, 2000, 95 (08) :2630-2636