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DOI: 10.1148/radiol.2301021085
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(Radiology 2004;230:55-64.)
© RSNA, 2004


Neuroradiology

Primary and Secondary Brain Tumors at MR Imaging: Bicentric Intraindividual Crossover Comparison of Gadobenate Dimeglumine and Gadopentetate Dimeglumine1

Michael V. Knopp, MD, PhD, Val M. Runge, MD, Marco Essig, MD, Marius Hartman, MD, Olav Jansen, MD, Miles A. Kirchin, PhD, Albrecht Moeller, PhD, Astrid H. Seeberg, PhD and Klaus-Peter Lodemann, PhD

1 From the Dept of Radiology, Ohio State Univ Hospitals, 657 Means Hall, 1654 Upham Dr, Columbus, OH 43210-1228 (M.V.K.); Scott and White Clinic and Hospital, Texas A&M Univ Health Science Ctr, Temple (V.M.R.); Dept of Radiology, German Cancer Research Ctr, Heidelberg (M.E.); Dept of Neuroradiology, Univ of Heidelberg, Germany (M.H.); Dept of Neuroradiology, Univ of Kiel, Germany (O.J.); Worldwide Medical Affairs, Bracco Imaging, Milan, Italy (M.A.K.); Medidata, Konstanz, Germany (A.M.); Bracco Altana Pharma, Konstanz, Germany (A.H.S., K.P.L.). Received Aug 30, 2002; revision requested Oct 28; final revision received May 13, 2003; accepted June 9. Address correspondence to M.V.K. (e-mail: knopp-1@medctr.osu.edu).

PURPOSE: To evaluate the safety of and compare the enhancement characteristics of gadobenate dimeglumine (MultiHance; Bracco Imaging, Milan, Italy) with those of a standard gadolinium chelate (gadopentetate dimeglumine, Magnevist; Schering, Berlin, Germany) in primary and secondary brain tumors on the basis of qualitative and quantitative parameters, on an intraindiviual basis.

MATERIALS AND METHODS: Twenty-seven patients with either high-grade glioma or metastases were enrolled in a bicentric intraindividual crossover study to compare lesion enhancement with doses of 0.1 mmol per kilogram of body weight of 0.5 mol/L gadopentetate dimeglumine and 0.5 mol/L gadobenate dimeglumine. MR imaging was performed before injection (T1-weighted spin-echo [SE] and T2-weighted fast SE acquisitions) and at 1, 3, 5, 7, 9, and 16 minutes after injection (T1-weighted SE acquisitions). Qualitative assessment was performed by blinded off-site readers (for 22 patients) and on-site investigators (for 24 patients) in terms of global contrast enhancement, lesion-to-brain contrast, lesion delineation, internal lesion morphology and structure, tumor vascularization, and global image preference. Additional quantitative assessment with region-of-interest analysis was performed by off-site readers alone. Statistical analysis of qualitative data was performed with the Wilcoxon signed rank test, whereas a nonparametric approach was adopted for analysis of quantitative data.

RESULTS: Significant (P < .05) preference for gadobenate dimeglumine over gadopentetate dimeglumine was noted both off-site and on-site for the global assessment of contrast enhancement. For off-site readers 1 and 2 and the on-site investigators, respectively, gadobenate dimeglumine was preferred in 13, 17, and 16 patients; gadopentetate dimeglumine was preferred in four, four, and four patients; and equality was found in five, one, and four patients). Similar preference for gadobenate dimeglumine was noted by off-site readers and on-site investigators for lesion-to-brain contrast and all other qualitative parameters. Off-site quantitative evaluation revealed significantly (P < .05) superior enhancement for gadobenate dimeglumine compared with that for gadopentetate dimeglumine at all time points from 3 minutes after injection.

CONCLUSION: Significantly superior contrast enhancement of intraaxial enhancing brain tumors was achieved with 0.1 mmol/kg gadobenate dimeglumine compared with that with 0.1 mmol/kg gadopentetate dimeglumine.

© RSNA, 2004

Index terms: Brain neoplasms, MR, 10.12143, 10.30 • Gadolinium • Magnetic resonance (MR), contrast media, 10.12143




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