Clinical biomarkers of angiogenesis inhibition

被引:45
作者
Brown, Aaron P. [2 ]
Citrin, Deborah E. [1 ]
Camphausen, Kevin A. [1 ]
机构
[1] NCI, Radiat Oncol Branch, Bethesda, MD 20892 USA
[2] NIH, Bethesda, MD 20892 USA
关键词
cancer; angiogenesis; biomarker; imaging;
D O I
10.1007/s10555-008-9143-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction An expanding understanding of the importance of angiogenesis in oncology and the development of numerous angiogenesis inhibitors are driving the search for biomarkers of angiogenesis. We review currently available candidate biomarkers and surrogate markers of anti-angiogenic agent effect. Discussion A number of invasive, minimally invasive, and non-invasive tools are described with their potential benefits and limitations. Diverse markers can evaluate tumor tissue or biological fluids, or specialized imaging modalities. Conclusions The inclusion of these markers into clinical trials may provide insight into appropriate dosing for desired biological effects, appropriate timing of additional therapy, prediction of individual response to an agent, insight into the interaction of chemotherapy and radiation following exposure to these agents, and perhaps most importantly, a better understanding of the complex nature of angiogenesis in human tumors. While many markers have potential for clinical use, it is not yet clear which marker or combination of markers will prove most useful.
引用
收藏
页码:415 / 434
页数:20
相关论文
共 295 条
[1]  
Abdollahi A, 2003, CANCER RES, V63, P8890
[2]   The human urinary proteome contains more than 1500 proteins, including a large proportion of membrane proteins [J].
Adachi, Jun ;
Kumar, Chanchal ;
Zhang, Yanling ;
Olsen, Jesper V. ;
Mann, Matthias .
GENOME BIOLOGY, 2006, 7 (09)
[3]   Impact and perceptions of mandatory tumor biopsies for correlative studies in clinical trials of novel anticancer agents [J].
Agulnik, Mark ;
Oza, Amit M. ;
Pond, Gregory R. ;
Siu, Lillian L. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (30) :4801-4807
[4]   Assessment of brain tumor angiogenesis inhibitors using perfusion magnetic resonance imaging: Quality and analysis results of a phase I trial [J].
Akella, NS ;
Twieg, DB ;
Mikkelsen, T ;
Hochberg, FH ;
Grossman, S ;
Cloud, GA ;
Nabors, LB .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2004, 20 (06) :913-922
[5]   Proteomic analysis to identify breast cancer biomarkers in nipple aspirate fluid [J].
Alexander, H ;
Stegner, AL ;
Wagner-Mann, C ;
Du Bois, GC ;
Alexander, S ;
Sauter, ER .
CLINICAL CANCER RESEARCH, 2004, 10 (22) :7500-7510
[6]   VASCULAR REACTIONS OF NORMAL AND MALIGNANT TISSUES INVIVO .1. VASCULAR REACTIONS OF MICE TO WOUNDS AND TO NORMAL AND NEOPLASTIC TRANSPLANTS [J].
ALGIRE, GH ;
CHALKLEY, HW .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1945, 6 (01) :73-85
[7]   Measurement of renal tumour and normal tissue perfusion using positron emission tomography in a phase II clinical trial of razoxane [J].
Anderson, H ;
Yap, JT ;
Wells, P ;
Miller, MP ;
Propper, D ;
Price, P ;
Harris, AL .
BRITISH JOURNAL OF CANCER, 2003, 89 (02) :262-267
[8]   Accuracy of whole-body dual-modality fluorine-18-2-fluoro-2-deoxy-D-glucose positron emission tomography and computed tomography (FDG-PET/CT) for tumor staging in solid tumors: Comparison with CT and PET [J].
Antoch, G ;
Saoudi, N ;
Kuehl, H ;
Dahmen, G ;
Mueller, SP ;
Beyer, T ;
Bockisch, A ;
Debatin, JF ;
Freudenberg, LS .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (21) :4357-4368
[9]  
Arora N, 1999, CANCER RES, V59, P183
[10]   Thalidomide and hematopoietic-cell transplantation for multiple myeloma [J].
Barlogie, B ;
Tricot, G ;
Anaissie, E ;
Shaughnessy, J ;
Rasmussen, E ;
van Rhee, F ;
Fassas, A ;
Zangari, M ;
Hollmig, K ;
Pineda-Roman, M ;
Lee, C ;
Talamo, G ;
Thertulien, R ;
Kiwan, E ;
Krishna, S ;
Fox, M ;
Crowley, J .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (10) :1021-1030