Detection of lymph node involvement in hematologic malignancies using micromagnetic resonance lymphangiography with a gadolinum-labeled dendrimer nanoparticle

被引:45
作者
Kobayashi, H
Kawamoto, S
Brechbiel, MW
Bernardo, M
Sato, N
Waldmann, TA
Tagaya, Y
Choyke, PL
机构
[1] NCI, Mol Imaging Program, Canc Res Ctr, NIH, Bethesda, MD 20892 USA
[2] Johns Hopkins Univ, Sch Med, Dept Radiol, Baltimore, MD 21218 USA
[3] NCI, Radiat Oncol Branch, Canc Res Ctr, NIH, Bethesda, MD 20892 USA
[4] NCI, Mol Imaging Program, Canc Res Ctr, SAIC Frederick,NIH, Frederick, MD 21701 USA
[5] NCI, Metab Branch, Canc Res Ctr, NIH, Bethesda, MD 20892 USA
来源
NEOPLASIA | 2005年 / 7卷 / 11期
关键词
malignant lymphoma; MRI; lymph node; lymphatic flow; nanoparticle;
D O I
10.1593/neo.05454
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Animal models of lymphoma should reflect their counterparts in humans; however, it can be difficult to ascertain whether an induced disease is intralymphatic or extralymphatic based on direct visualization. Current imaging methods are insufficient for identifying lymphatic and intralymphatic involvement. To differentiate intralymphatic from extralymphatic involvement, we have developed a magnetic resonance imaging-based lymphangiography method and tested it on two animal models of lymphoma. A gadolinium (Gd)-labeled dendrimer nanoparticle (generation-6; similar to 220 kDa/similar to 10 nm) was injected interstitially into mice bearing hematologic malignancies to perform dynamic micromagnetic resonance lymphangiography (micro-MRIL). Both a standard T1-weighted 3D fast spoiled gradient echo and a T2/T1-weighted D-fast imaging employing steady-state acquisition (3D-FIESTA-C) were compared in an imaging study to differentiate intralymphatic from extralymphatic involvement of tumors. The lymphatics and lymph nodes were visualized with both methods in all cases. In addition, 3D-FIESTA-C depicted both the lymphatic system and the extralymphatic tumor. In an animal model, 3D-FIESTA-C demonstrated that the bulk of the tumor thought to be intralymphatic was actually extralymphatic. In conclusion, micro-MRL, using Gd-labeled dendrimer nanoparticles with the combined method, can define both the normal and abnormal lymphatics and can distinguish intralymphatic from extralymphatic diseases in mouse models of malignant lymphoma.
引用
收藏
页码:984 / 991
页数:8
相关论文
共 34 条
[1]  
ARMITAGE JO, 2004, HARRISONS PRINCIPLES, P641
[2]  
BRUNA J, 1988, LYMPHOLOGY, V21, P178
[3]  
Buscombe JR, 2004, Q J NUCL MED MOL IM, V48, P109
[4]   Intra-alveolar hemorrhage following bipedal lymphography [J].
Dupont, H ;
Timsit, JF ;
Souweine, B ;
Gachot, B ;
Bedos, JP ;
Wolff, M .
INTENSIVE CARE MEDICINE, 1996, 22 (06) :614-615
[5]   Comparison of whole-body MRI with automatic moving table technique and bone scintigraphy for screening for bone metastases in patients with breast cancer [J].
Engelhard, K ;
Hollenbach, HP ;
Wohlfart, K ;
von Imhoff, E ;
Fellner, FA .
EUROPEAN RADIOLOGY, 2004, 14 (01) :99-105
[6]   Whole body turbo STIR MRI in unknown primary tumor detection [J].
Eustace, S ;
Tello, R ;
DeCarvalho, V ;
Carey, J ;
Melhem, E ;
Yucel, EK .
JMRI-JOURNAL OF MAGNETIC RESONANCE IMAGING, 1998, 8 (03) :751-753
[7]  
FISCHER P, 1988, BLOOD, V72, P234
[8]   A hydrochemical modelling framework for combined assessment of spatial and temporal variability in stream chemistry: application to Plynlimon, Wales [J].
Foster, HJ ;
Lees, MJ ;
Wheater, HS ;
Neal, C ;
Reynolds, B .
HYDROLOGY AND EARTH SYSTEM SCIENCES, 2001, 5 (01) :49-58
[9]   Whole-body FDG-PET imaging in the management of patients with cancer [J].
Hustinx, R ;
Bénard, F ;
Alavi, A .
SEMINARS IN NUCLEAR MEDICINE, 2002, 32 (01) :35-46
[10]   Whole-body turbo STIR MR imaging: controversies and avenues for development [J].
Kavanagh, E ;
Smith, C ;
Eustace, S .
EUROPEAN RADIOLOGY, 2003, 13 (09) :2196-2205