Angiogenic inhibitors: a new therapeutic strategy in oncology

被引:179
作者
Gasparini, G
Longo, R
Toi, M
Ferrara, N
机构
[1] San Filippo Neri Hosp, Div Med Oncol, Rome, Italy
[2] Tokyo Metropolitan Canc, Dept Clin Trials & Res, Tokyo, Japan
[3] Komagome Hosp, Ctr Infect Dis, Tokyo, Japan
来源
NATURE CLINICAL PRACTICE ONCOLOGY | 2005年 / 2卷 / 11期
关键词
antiangiogenic therapy; bevacizumab; SU11248; tyrosine kinase inhibitors; VEGF;
D O I
10.1038/ncponc0342
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Angiogenesis is a multistep, complex and tightly regulated process that is necessary for tumor growth and metastasis. Based on data of preclinical models, several antiangiogenic compounds has been shown to modify activated tumor endothelium, which suggests that these compounds can improve cytotoxic drug delivery. Such agents have entered clinical trials as single agents or in combination with cytotoxic drugs, and have shown promising antitumor activity. The pharmacodynamic and pharmacokinetic characteristics of antiangiogenic drugs are reviewed here. Most of the early clinical testing of these agents was conducted in patients with advanced disease resistant to standard therapies. Phase III trials compared the efficacy of standard chemotherapy alone with standard chemotherapy in combination with an experimental angiogenesis inhibitor. Although some of these studies were negative or controversial, recent studies validated in large clinical trials with an anti-vascular endothelial growth factor antibody demonstrated significant clinical benefit and renewed enthusiasm for this therapeutic strategy. This review describes the clinical studies of antiangiogenic agents and highlights the challenges related to choosing appropriate strategies for the selection of patients, study design and choice of appropriate endpoints for the studies' development.
引用
收藏
页码:562 / 577
页数:16
相关论文
共 100 条
  • [1] AHMAD T, 2004, P AM SOC CLIN ONCOL, V22
  • [2] Celecoxib, a selective cyclo-oxygenase-2 inhibitor, enhances the response to preoperative paclitaxel and carboplatin in early-stage non-small-cell lung cancer
    Altorki, NK
    Keresztes, RS
    Port, JL
    Libby, MD
    Korst, RJ
    Flieder, DB
    Ferrara, CA
    Yankelevitz, DF
    Subbaramaiah, K
    Pasmantier, MW
    Dannenberg, AJ
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (14) : 2645 - 2650
  • [3] Extended survival in advanced and refractory multiple myeloma after single-agent thalidomide: identification of prognostic factors in a phase 2 study of 169 patients
    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
    [J]. BLOOD, 2001, 98 (02) : 492 - 494
  • [4] Differential effects of vascular endothelial growth factor receptor-2 inhibitor ZD6474 on circulating endothelial progenitors and mature circulating endothelial cells: Implications for use as a surrogate marker of antiangiogenic activity
    Beaudry, P
    Force, J
    Naumov, GN
    Wang, A
    Baker, CH
    Ryan, A
    Soker, S
    Johnson, BE
    Folkman, J
    Heymach, JV
    [J]. CLINICAL CANCER RESEARCH, 2005, 11 (09) : 3514 - 3522
  • [5] Tumorigenesis and the angiogenic switch
    Bergers, G
    Benjamin, LE
    [J]. NATURE REVIEWS CANCER, 2003, 3 (06) : 401 - 410
  • [6] Update on clinical trials targeting vascular endothelial growth factor in cancer
    Bergsland, EK
    [J]. AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 2004, 61 (21) : S12 - S20
  • [7] Bertolini F, 2003, CANCER RES, V63, P4342
  • [8] Influence of unrecognized molecular heterogeneity on randomized clinical trials
    Betensky, RA
    Louis, DN
    Cairncross, JG
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (10) : 2495 - 2499
  • [9] Cardiovascular events associated with rofecoxib in a colorectal adenoma chemoprevention trial
    Bresalier, RS
    Sandler, RS
    Quan, H
    Bolognese, JA
    Oxenius, B
    Horgan, K
    Lines, C
    Riddell, R
    Morton, D
    Lanas, A
    Konstam, MA
    Baron, JA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (11) : 1092 - 1102
  • [10] Brown LF, 1999, CLIN CANCER RES, V5, P1041