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Neuroradiology |
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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