Clinical trials of antiangiogenic therapy in non-small cell lung cancer: focus on bevacizumab and ZD6474

被引:8
作者
Morgensztern, Daniel [1 ]
Govindan, Ramaswamy [1 ]
机构
[1] St Louis Univ, Sch Med, Alvin J Siteman Canc Ctr, Div Oncol, St Louis, MO 63110 USA
关键词
antiangiogenic therapy; bevacizumab; non-small cell; lung cancer; ZD6474;
D O I
10.1586/14737140.6.4.545
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer is the leading cause of cancer deaths in the USA. Despite the development of new chemotherapy regimens, the prognosis remains poor. Several studies comparing various platinum-based regimens failed to produce a significant impact in the outcomes for patients with non-small cell lung cancer and this therapeutic modality appears to be reaching a plateau. It has become clear that further advances will require the addition of agents with a different mechanism of action. Bevacizumab is the antianglogenic agent at the most advanced stage of development in the treatment of cancer. Bevaclzumab is synergistic with chemotherapy and usually well tolerated. The addition of bevacizurnab to chemotherapy improved survival in patients with metastatic non-small cell lung cancer in a randomized clinical trial. Several small molecule antlanglogenic agents are in development. In this article, currently available data from clinical trials of antiangiogenic compounds in advanced non-small cell lung cancer are reviewed.
引用
收藏
页码:545 / 551
页数:7
相关论文
共 33 条
[1]  
Camp ER, 2005, CLIN CANCER RES, V11, P397
[2]   Angiogenesis in life, disease and medicine [J].
Carmeliet, P .
NATURE, 2005, 438 (7070) :932-936
[3]   Angiogenesis in health and disease [J].
Carmeliet, P .
NATURE MEDICINE, 2003, 9 (06) :653-660
[4]  
Ciardiello F, 2003, CLIN CANCER RES, V9, P1546
[5]   Investigating the potential of bevacizumab in other indications: Metastatic renal cell, non-small cell lung, pancreatic and breast cancer [J].
de Gramont, A ;
Van Cutsem, E .
ONCOLOGY, 2005, 69 :46-56
[6]   Vascular permeability factor/vascular endothelial growth factor: A critical cytokine in tumor angiogenesis and a potential target for diagnosis and therapy [J].
Dvorak, HF .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (21) :4368-4380
[7]   Use of angiogenesis inhibitors in tumour treatment [J].
Fayette, M ;
Soria, JC ;
Armand, JP .
EUROPEAN JOURNAL OF CANCER, 2005, 41 (08) :1109-1116
[8]   The biology of VEGF and its receptors [J].
Ferrara, N ;
Gerber, HP ;
LeCouter, J .
NATURE MEDICINE, 2003, 9 (06) :669-676
[9]   Seminars in medicine of the Beth Israel Hospital, Boston - Clinical applications of research on angiogenesis [J].
Folkman, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (26) :1757-1763
[10]   Phase I safety and pharmacokinetic study of recombinant human anti-vascular endothelial growth factor in patients with advanced cancer [J].
Gordon, MS ;
Margolin, K ;
Talpaz, M ;
Sledge, GW ;
Holmgren, E ;
Benjamin, R ;
Stalter, S ;
Shak, S ;
Adelman, DC .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (03) :843-850