Diagnosis and Evaluation


39th ASCO Annual Meeting. Chicago, IL. May 31-June 3, 2003. Abstract No. 488 (Clinical Study)


Meeting Abstract

Ferumoxtran-10 enhanced MR in variety of intracranial tumors and other lesions

E. A. Neuwelt, L. Konyves-Kolonics, M. Haluska

Oregon Health & Science Univ, Portland, OR

Ultrasmall particulate iron oxides (USPIO) are used in magnetic resonance imaging (MRI) as contrast agents due to shortening of T1 and T2 relaxation time.
Ferumoxtran-10 (Combidex), a dextran coated viral sized iron nanoparticle has a long plasma half-life of 24-30 hours resulting in prolonged and progressive accumulation in human intracranial lesions.
The distribution, intensity, and time course of MR enhancement with Ferumoxtran was compared to standard gadolinium (GD) enhanced MR in assessing different types of intracranial lesions, including malignant tumors, vascular malformations and demyelinating disorders.
All malignant lesions were histologically proven by surgery or biopsy.
34 studies of 33 patients were analyzed.
All of the patients had a standard brain MR with and without GD.
The dose of Ferumoxtran-10 was 2.6 mg/kg infused intravenously.
The post-iron study includes 24 hours and 48 hours investigations and some patients also had 3 hours, 6 hours or 72 hours studies.
MR scans included SET1, FST2 and proton density (PD), GRET2*, DWI and EPIT2.
Most lesions detected with GD were also detected with USPIO.
In 6 of 33 patients iron enhanced studies showed a larger area of enhancement compared to GD.
In 2 patients USPIO showed new areas of enhancement not present on the gadolinium study.
Regarding the time-course, in 4 patients stronger intensity and larger area of iron accumulation were detected in consecutive studies consistent with progressive iron uptake.
In 21 patients no significant differences were detected or GD showed more intensive enhancement but the same volume of enhancement.
USPIO can add new information on different types of intracranial lesions, particularly malignant tumors, regarding volume of enhancement, and in some cases additional lesions can be identified.

© Copyright 2003 American Society of Clinical Oncology All rights reserved worldwide

Source: http://www.asco.org/ac/1,1003,_12-002489-00_18-002003-00_19-00104321-00_29-00A,00.asp?cat=CNS+Tumors&parent=
Central+Nervous+System+Tumors&returnpid=2325&SubCat_ID=4



 

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