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Volume 49, Issue 2, Pages 217-222 (August 2008)


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Doxorubicin-eluting bead-enhanced radiofrequency ablation of hepatocellular carcinoma: A pilot clinical study

Riccardo Lencioni1Corresponding Author Informationemail address, Laura Crocetti1, Pasquale Petruzzi1, Claudio Vignali1, Elena Bozzi1, Clotilde Della Pina1, Irene Bargellini1, Dania Cioni1, Filippo Oliveri2, Paolo De Simone3, Carlo Bartolozzi1, Maurizia Brunetto2, Franco Filipponi3

Received 27 December 2007; received in revised form 1 March 2008; accepted 26 March 2008. published online 24 April 2008.

Background/Aims

Experimental studies have shown synergy between radiofrequency (RF) ablation and adjuvant chemotherapy in animal tumour models. We aimed to assess safety and efficacy of doxorubicin-eluting bead (DEB)-enhanced RF ablation in the treatment of human hepatocellular carcinoma (HCC).

Methods

Twenty patients with single HCC ranging 3.3–7.0cm (mean, 5.0cm±1.4) showing evidence of residual viable tumour after standard RF ablation underwent intraarterial DEB administration (50–125mg doxorubicin; mean, 60.2mg±21.8). Follow-up period ranged 6–20 months (mean, 12 months±5).

Results

No major complication occurred. No deterioration of liver function was observed. The volume of treatment-induced necrosis – as measured on imaging – increased from 48.1cm3±35.7 after RF ablation to 75.5cm3±52.4 after DEB administration, with an increase of 60.9%±39.0. The enhanced effect resulted in confirmed complete response (CR) of the target lesion in 12 (60%) of 20 patients. Incomplete response with persistence of <10% of initial tumour volume was observed in 6 (30%) of 20 patients, and local tumour progression in 2 (10%) of 20.

Conclusions

Intraarterial DEB administration substantially enhances the effect of RF ablation. DEB-enhanced RF ablation is safe and results in a high rate of CR in patients refractory to standard RF treatment.

Associate Editor: M. Colombo

1 Division of Diagnostic and Interventional Radiology, Department of Oncology and Radiology, Cisanello University Hospital – Building No. 9, Via Paradisa 2, IT-56124 Pisa, Italy

2 Division of Hepatology, Department of Liver Transplantation, Hepatology, and Infectious Diseases, Cisanello University Hospital, Via Paradisa 2, IT-56124 Pisa, Italy

3 Division of Liver Transplantation, Department of Liver Transplantation, Hepatology, and Infectious Diseases, Cisanello University Hospital, Via Paradisa 2, IT-56124 Pisa, Italy

Corresponding Author InformationCorresponding author. Tel.: +39 050 992 509; fax: +39 050 551 461.

 The authors who have taken part in the research of this paper declared that they do not have a relationship with the manufacturers of the materials involved either in the past or present and they did not receive funding from the manufacturers to carry out their research.

PII: S0168-8278(08)00242-0

doi:10.1016/j.jhep.2008.03.021


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