Combination of antiangiogenic therapy with other anticancer therapies: Results, challenges, and open questions

被引:170
作者
Gasparini, G
Longo, R
Fanelli, M
Teicher, BA
机构
[1] Azienda Complesso Osped S Filippo Neri, Div Med Oncol, I-00135 Rome, Italy
[2] Genzyme Corp, Framingham, MA 01701 USA
关键词
D O I
10.1200/JCO.2005.10.022
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Angiogenesis is necessary for tumor growth. Drug discovery efforts have identified several potential therapeutic targets on endothelial cells and selective inhibitors capable of slowing tumor growth or producing tumor regression by blocking angiogenesis in in vivo tumor models. Certain antiangiogenic therapeutics increase the activity of cytotoxic anticancer treatments in preclinical models. More than 75 antiangiogenic compounds have entered clinical trials. Most of the early clinical testing was conducted in patients with advanced disease resistant to standard therapies. Several phase III trials have been undertaken to compare the efficacy of standard chemotherapy versus the same in combination with an experimental angiogenesis inhibitor. Preliminary results of the clinical studies suggest that single-agent antiangiogenic therapy is poorly active in advanced tumors. Although some of the results of combination trials are controversial, recent positive outcomes with an antivascular endothelial growth factor antibody combined with chemotherapy as front-line therapy of metastatic colorectal cancer have renewed enthusiasm for this therapeutic strategy. This article presents an overview of experimental and clinical studies of combined therapy with antiangiogenic agents and highlights the challenges related to the appropriate strategies for selection of the patients, study design, and choice of proper end points for preclinical and clinical studies using these agents.
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页码:1295 / 1311
页数:17
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共 167 条
[1]  
AKLILU M, 2002, P AN M AM SOC CLIN, V21, pB28
[2]   Celecoxib, a selective cyclo-oxygenase-2 inhibitor, enhances the response to preoperative paclitaxel and carboplatin in early-stage non-small-cell lung cancer [J].
Altorki, NK ;
Keresztes, RS ;
Port, JL ;
Libby, MD ;
Korst, RJ ;
Flieder, DB ;
Ferrara, CA ;
Yankelevitz, DF ;
Subbaramaiah, K ;
Pasmantier, MW ;
Dannenberg, AJ .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (14) :2645-2650
[3]   Assessment of pharmacodynamic vascular response in a phase I trial of combretastatin A4 phosphate [J].
Anderson, HL ;
Yap, JT ;
Miller, MP ;
Robbins, A ;
Jones, T ;
Price, PM .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (15) :2823-2830
[4]  
ANDERSON I, 1999, P AN M AM SOC CLIN, V18, pA187
[5]  
[Anonymous], **NON-TRADITIONAL**
[6]  
[Anonymous], 1994, RADIAT ONCOL INVEST
[7]   Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization [J].
Asahara, T ;
Masuda, H ;
Takahashi, T ;
Kalka, C ;
Pastore, C ;
Silver, M ;
Kearne, M ;
Magner, M ;
Isner, JM .
CIRCULATION RESEARCH, 1999, 85 (03) :221-228
[8]   SIMPLE PROCEDURE FOR LONG-TERM CULTIVATION OF CHICKEN EMBRYOS [J].
AUERBACH, R ;
KUBAI, L ;
KNIGHTON, D ;
FOLKMAN, J .
DEVELOPMENTAL BIOLOGY, 1974, 41 (02) :391-394
[9]  
Bacharach SL, 2002, J NUCL MED, V43, P1542
[10]  
Bagley RG, 2003, CANCER RES, V63, P5866