Parametric imaging of tumor perfusion using flow- and permeability-limited tracers

被引:36
作者
Bogin, L [1 ]
Margalit, R [1 ]
Mispelter, J [1 ]
Degani, H [1 ]
机构
[1] Weizmann Inst Sci, Dept Regulat Biol, IL-76100 Rehovot, Israel
关键词
deuterium MRI; constrast-enhanced MRI; perfusion; breast cancer;
D O I
10.1002/jmri.10159
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
Purpose: To quantitatively evaluate the spatial distribution of flow- and permeability-limited perfusion in MCF7 human breast cancer tumors orthotopically implanted in CD1-NU mice. Materials and Methods: Flow-limited perfusion was derived from H-2-MRI recorded before and after infusion of deuterated water. Permeability-limited perfusion was evaluated from GdDTPA-enhanced H-1-MRI. Results: The dominant processes in tumor perfusion, namely blood flow and capillary permeability, were mapped in orthotopically implanted MCF7 human breast cancer tumors. The dynamic data were processed according to physiological models, yielding parametric maps of intravascular volume fraction, water perfusion rate, GdDTPA permeability rate constant, and extracellular volume fraction accessible to GdDTPA. The maps exhibited the heterogenous distribution of each perfusion parameter. Most of the tumor tissue (greater than or equal to95%) was perfused with HDO, while GdDTPA was perfused in only about 50% of it. In most loci the perfusion rate was limited by capillary permeability to GdDTPA. Conclusion: The results demonstrated the instructive value of tracers with different properties used in conjunction to achieve a deeper understanding of tumor perfusion capacity. This study offers tools for the accurate, noninvasive evaluation of drug delivery efficacy.
引用
收藏
页码:289 / 299
页数:11
相关论文
共 43 条
[1]   DEUTERIUM NUCLEAR-MAGNETIC-RESONANCE MEASUREMENTS OF BLOOD-FLOW AND TISSUE PERFUSION EMPLOYING (H2O)-H-2 AS A FREELY DIFFUSIBLE TRACER [J].
ACKERMAN, JJH ;
EWY, CS ;
BECKER, NN ;
SHALWITZ, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (12) :4099-4102
[2]  
ALTMAN PL, 1974, BIOL DATABOOK, P1988
[3]  
Barbour H G, 1937, Yale J Biol Med, V9, P551
[4]   Effect of antiangiogenic therapy on slowly growing, poorly vascularized tumors in mice [J].
Beecken, WDC ;
Fernandez, A ;
Joussen, AM ;
Achilles, EG ;
Flynn, E ;
Lo, KM ;
Gillies, SD ;
Javaherian, K ;
Folkman, J ;
Shing, Y .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2001, 93 (05) :382-387
[5]   Hypoxia:: the tumor's gateway to progression along the angiogenic pathway [J].
Brahimi-Horn, C ;
Berra, E ;
Pouysségur, J .
TRENDS IN CELL BIOLOGY, 2001, 11 (11) :S32-S36
[6]   PHARMACOKINETIC PARAMETERS IN CNS GD-DTPA ENHANCED MR IMAGING [J].
BRIX, G ;
SEMMLER, W ;
PORT, R ;
SCHAD, LR ;
LAYER, G ;
LORENZ, WJ .
JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY, 1991, 15 (04) :621-628
[7]   MRI techniques in early stages of cartilage disease [J].
Burstein, D ;
Bashir, A ;
Gray, ML .
INVESTIGATIVE RADIOLOGY, 2000, 35 (10) :622-638
[8]   Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[9]   Endothelial signal integration in vascular assembly [J].
Daniel, TO ;
Abrahamson, D .
ANNUAL REVIEW OF PHYSIOLOGY, 2000, 62 :649-671
[10]   Mapping pathophysiological features of breast tumors by MRI at high spatial resolution [J].
Degani, H ;
Gusis, V ;
Weinstein, D ;
Fields, S ;
Strano, S .
NATURE MEDICINE, 1997, 3 (07) :780-782