Dynamic contrast-enhanced MRI in clinical oncology: Current status and future directions

被引:364
作者
Padhani, AR [1 ]
机构
[1] Mt Vernon Hosp, Paul Strickland Scanner Ctr, Northwood HA6 2RN, Middx, England
关键词
dynamic contrast-enhanced MRI; angiogenesis; macromolecular contrast media; antiangiogenic drugs; antivascular therapies;
D O I
10.1002/jmri.10176
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) is performed after the administration of intravenous contrast medium to noninvasively access tumor vascular characteristics. DCE-MRI techniques utilizing low-molecular-weight contrast media have successfully made the transition from methodological development to preclinical and clinical validation and are now rapidly becoming mainstream clinical tools. DCE-MRI using macromolecular contrast medium (MMCM) can also assay microvascular characteristics of human tumor xenografts. MMCM approval for human use will occur soon. The success of both techniques depends on their ability to demonstrate quantitative differences of contrast medium behavior in a variety of tissues. Evidence is mounting that kinetic parameters correlate with immunohistochemical surrogates of tumor angiogenesis, including microvessel density, and with pathologic tumor grade. DCE-MRI is being applied to monitor the clinical effectiveness of a variety of treatments, including antiangiogenic drugs. Kinetic parameter changes following treatment have correlated with histopathological outcome and patient survival. This article reviews the current clinical status of low-molecular-weight DCE-MRI and reviews the potential of MMCM techniques for evaluating human tumors. Ongoing challenges faced by DCE-MRI as clinical and research tools will be explored.
引用
收藏
页码:407 / 422
页数:16
相关论文
共 219 条
[1]   Differentiation of spontaneous canine breast tumors using dynamic magnetic resonance imaging with 24-gadolinium-DTPA-cascade-polymer, a new blood-pool agent - Preliminary experience [J].
Adam, G ;
Muhler, A ;
Spuntrup, E ;
Neuerburg, JM ;
Kilbinger, M ;
Bauer, H ;
Fucezi, L ;
Kupper, W ;
Gunther, RW .
INVESTIGATIVE RADIOLOGY, 1996, 31 (05) :267-274
[2]  
ARONEN HJ, 1995, ACTA RADIOL, V36, P520
[3]   CEREBRAL BLOOD-VOLUME MAPS OF GLIOMAS - COMPARISON WITH TUMOR GRADE AND HISTOLOGIC-FINDINGS [J].
ARONEN, HJ ;
GAZIT, IE ;
LOUIS, DN ;
BUCHBINDER, BR ;
PARDO, FS ;
WEISSKOFF, RM ;
HARSH, GR ;
COSGROVE, GR ;
HALPERN, EF ;
HOCHBERG, FH ;
ROSEN, BR .
RADIOLOGY, 1994, 191 (01) :41-51
[4]   Gliomas: Correlation of magnetic susceptibility artifact with histologic grade [J].
Bagley, LJ ;
Grossman, RI ;
Judy, KD ;
Curtis, M ;
Loevner, LA ;
Polansky, M ;
Detre, J .
RADIOLOGY, 1997, 202 (02) :511-516
[5]  
Barbier EL, 1999, JMRI-J MAGN RESON IM, V10, P242, DOI 10.1002/(SICI)1522-2586(199909)10:3<242::AID-JMRI4>3.0.CO
[6]  
2-H
[7]   Methodology of brain perfusion imaging [J].
Barbier, EL ;
Lamalle, L ;
Décorps, M .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2001, 13 (04) :496-520
[8]   Staging urinary bladder cancer after transurethral biopsy: Value of fast dynamic contrast-enhanced MR imaging [J].
Barentsz, JO ;
Jager, GJ ;
vanVierzen, PBJ ;
Witjes, JA ;
Strijk, SP ;
Peters, H ;
Karssemeijer, N ;
Ruijs, SHJ .
RADIOLOGY, 1996, 201 (01) :185-193
[9]   Evaluation of chemotherapy in advanced urinary bladder cancer with fast dynamic contrast-enhanced MR imaging [J].
Barentsz, JO ;
Berger-Hartog, O ;
Witjes, JA ;
Hulsbergen-van der Kaa, C ;
Oosterhof, GON ;
VanderLaak, JAWM ;
Kondacki, H ;
Ruijs, SHJ .
RADIOLOGY, 1998, 207 (03) :791-797
[10]  
Bhujwalla Z M, 1999, Top Magn Reson Imaging, V10, P92, DOI 10.1097/00002142-199904000-00002