Prospective Randomized Study of Doxorubicin-Eluting-Bead Embolization in the Treatment of Hepatocellular Carcinoma: Results of the PRECISION V Study
Male
Carcinoma, Hepatocellular
Doxorubicin/ administration & dosage
Aged; Antibiotics, Antineoplastic/administration & dosage; Carcinoma, Hepatocellular/therapy; Chemoembolization, Therapeutic/methods; Doxorubicin/administration & dosage; Drug Carriers; Drug Implants; Female; Humans; Liver Neoplasms/therapy; Male; Prospective Studies; Single-Blind Method; Treatment Outcome
610
610 Medicine & health
Chemoembolization, Therapeutic/ methods
2705 Cardiology and Cardiovascular Medicine
03 medical and health sciences
0302 clinical medicine
info:eu-repo/classification/ddc/617
Antibiotics, Antineoplastic/ administration & dosage
2741 Radiology, Nuclear Medicine and Imaging
Humans
Single-Blind Method
Clinical Investigation
Prospective Studies
Chemoembolization, Therapeutic
Aged
Drug Implants
Drug Carriers
Antibiotics, Antineoplastic
ddc:617
10042 Clinic for Diagnostic and Interventional Radiology
Liver Neoplasms/ therapy
Liver Neoplasms
Carcinoma, Hepatocellular/ therapy
3. Good health
Treatment Outcome
Radiology Nuclear Medicine and imaging
Doxorubicin
Female
Cardiology and Cardiovascular Medicine
DOI:
10.1007/s00270-009-9711-7
Publication Date:
2009-11-11T19:36:04Z
AUTHORS (21)
ABSTRACT
Transcatheter arterial chemoembolization (TACE) offers a survival benefit to patients with intermediate hepatocellular carcinoma (HCC). A widely accepted TACE regimen includes administration of doxorubicin-oil emulsion followed by gelatine sponge-conventional TACE. Recently, a drug-eluting bead (DC Bead) has been developed to enhance tumor drug delivery and reduce systemic availability. This randomized trial compares conventional TACE (cTACE) with TACE with DC Bead for the treatment of cirrhotic patients with HCC. Two hundred twelve patients with Child-Pugh A/B cirrhosis and large and/or multinodular, unresectable, N0, M0 HCCs were randomized to receive TACE with DC Bead loaded with doxorubicin or cTACE with doxorubicin. Randomization was stratified according to Child-Pugh status (A/B), performance status (ECOG 0/1), bilobar disease (yes/no), and prior curative treatment (yes/no). The primary endpoint was tumor response (EASL) at 6 months following independent, blinded review of MRI studies. The drug-eluting bead group showed higher rates of complete response, objective response, and disease control compared with the cTACE group (27% vs. 22%, 52% vs. 44%, and 63% vs. 52%, respectively). The hypothesis of superiority was not met (one-sided P = 0.11). However, patients with Child-Pugh B, ECOG 1, bilobar disease, and recurrent disease showed a significant increase in objective response (P = 0.038) compared to cTACE. DC Bead was associated with improved tolerability, with a significant reduction in serious liver toxicity (P < 0.001) and a significantly lower rate of doxorubicin-related side effects (P = 0.0001). TACE with DC Bead and doxorubicin is safe and effective in the treatment of HCC and offers a benefit to patients with more advanced disease.
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