Local Arterial Infusion of Superparamagnetic Iron Oxide Particles in Hepatocellular Carcinoma: A Feasibility and 3.0 T MRI Study

OBJECTIVES:We sought to prove feasibility of selective arterial infusion of superparamagnetic iron oxide (SPIO) particles in patients with hepatocellular carcinoma (HCC). MATERIALS AND METHODS:We studied 13 patients with HCC who underwent modified transarterial chemoembolization (TACE). Six patients...

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Veröffentlicht in:Investigative radiology 2006-06, Vol.41 (6), p.527-535
Hauptverfasser: Dudeck, Oliver, Bogusiewicz, Katarzyna, Pinkernelle, Jens, Gaffke, Gunnar, Pech, Maciej, Wieners, Gero, Bruhn, Harald, Jordan, Andreas, Ricke, Jens
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Sprache:eng
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Zusammenfassung:OBJECTIVES:We sought to prove feasibility of selective arterial infusion of superparamagnetic iron oxide (SPIO) particles in patients with hepatocellular carcinoma (HCC). MATERIALS AND METHODS:We studied 13 patients with HCC who underwent modified transarterial chemoembolization (TACE). Six patients received concurrent infusion of Ferucarbotran (Resovist, Schering, Berlin, Germany) in tumor-feeding arteries, and another 6 received MFL AS (MagForce, Nanotechnologies, Berlin, Germany). The iron content of both dispersions was 3.92 mg. One patient served as a control. All patients underwent magnetic resonance imaging (MRI) as baseline and immediate follow-up investigation. RESULTS:Selective arterial infusion of both SPIO particles resulted in significant intratumoral signal intensity decrease on T1-weighted sequences (P < 0.0001), which was greater after MagForce infusion compared with Resovist (P = 0.002). Only minimal amounts of dispersed particles were found in adjacent normal liver parenchyma. No change in intratumoral signal intensity was noted when ferromagnetic particles were omitted. CONCLUSIONS:Modified TACE with selective arterial infusion of SPIO particles can be used for precise tumor targeting in patients with HCC, for which MagForce appeared superior to Resovist.
ISSN:0020-9996
1536-0210
DOI:10.1097/01.rli.0000209601.15533.5a