Transarterial chemoembolization of unresectable hepatocellular carcinoma with drug eluting beads: Results of an open-label study of 62 patients

被引:176
作者
Malagari, Katerina [1 ]
Chatzimichael, Katerina [1 ]
Alexopoulou, Efthymia [1 ]
Kelekis, Alexios [1 ]
Hall, Brenda [5 ]
Dourakis, Spyridon [2 ,3 ]
Delis, Spyridon [4 ]
Gouliamos, Athanasios [1 ]
Kelekis, Dimitrios [6 ]
机构
[1] Univ Athens, Dept Radiol 2, Athens 12462, Greece
[2] Univ Athens, Clin Internal Med & Hepatol 2, Athens, Greece
[3] Ippokrat Hosp Univ Athens, Dept Internal Med & Hepatol, Athens, Greece
[4] Agia Olga Hosp, Dept Surg, Athens, Greece
[5] Biocompatibles UK Inc, Surrey, England
[6] Univ Athens, Evgenidion Hosp, Res Ctr Radiol & Imaging, Athens 11538, Greece
关键词
hepatocellular carcinoma; doxorubicin; embolization; drug-eluting beads;
D O I
10.1007/s00270-007-9226-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The purpose of this study was to assess the safety and efficacy of doxorubicin-loaded beads (DC Beads) delivered by transarterial embolization for the treatment of unresectable hepatocellular carcinoma (HCC). This open-label, single-center, single-arm study included 62 cirrhotic patients with documented single unresectable HCC. Mean tumor diameter was 5.6 cm (range, 3-9 cm) classified as Okuda stages 1 (n = 53) and 2 (n = 9). Patients received repeat embolizations with doxorubicin-loaded beads every 3 months (maximum of three). The maximum doxorubicin dose was 150 mg per embolization, loaded in DC Beads of 100-300 or 300-500 mu m. Regarding efficacy, overall, an objective response according to the European Association for the Study of the Liver criteria was observed in 59.6%, 81.8%, and 70.8% across three treatments. A complete response was observed in 4.8% after the first procedure and 3.6% and 8.3% after the second and third procedures, respectively. At 9 months a complete response was seen in 12.2%, an objective response in 80.7%, progressive disease in 6.8%, and 12.2% showed stable disease. Mean tumor necrosis ranged from 77.4% to 83.9% (range, 28.6%-100%) across three treatments. alpha-Fetoprotein levels showed a mean decrease of 1123 ng/ml (95% CI = 846-1399; p = 3 x 10(-11)) after the first session and remained stable after the second and third embolizations (42 and 70 ng/ml decrease, respectively). Regarding safety, bilirubin, gamma-glutamyl transferase, aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase showed only transient increases during the study period. Severe procedure-related complications were seen in 3.2% (cholecystitis, n = 1; liver abscess, n = 1). Postembolization syndrome was observed in all patients. We conclude that hemoembolization using doxorubicin-loaded DC Beads is a safe and effective treatment of HCC as demonstrated by the low complication rate, increased tumor response, and sustained reduction of alpha-fetoprotein levels.
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收藏
页码:269 / 280
页数:12
相关论文
共 38 条
[1]   In vitro stability of tris-acryl gelatin microspheres in a multipharmaceutical chemoembolization solution [J].
Ball, DS ;
Heckman, R ;
Olenick, SW ;
Folander, HL ;
Reed, J .
JOURNAL OF VASCULAR AND INTERVENTIONAL RADIOLOGY, 2003, 14 (01) :83-88
[2]   Society of interventional radiology position statement on chemoembolization of hepatic malignancies [J].
Brown, DB ;
Geschwind, JFH ;
Soulen, MC ;
Millward, SF ;
Sacks, D .
JOURNAL OF VASCULAR AND INTERVENTIONAL RADIOLOGY, 2006, 17 (02) :217-223
[3]   Transarterial embolization versus symptomatic treatment in patients with advanced hepatocellular carcinoma:: Results of a randomized, controlled trial in a single institution [J].
Bruix, J ;
Llovet, JM ;
Castells, A ;
Montañá, X ;
Brú, C ;
Ayuso, MD ;
Vilana, R ;
Rodés, J .
HEPATOLOGY, 1998, 27 (06) :1578-1583
[4]   Clinical management of hepatocellular carcinoma.: Conclusions of the Barcelona-2000 EASL Conference [J].
Bruix, J ;
Sherman, M ;
Llovet, JM ;
Beaugrand, M ;
Lencioni, R ;
Burroughs, AK ;
Christensen, E ;
Pagliaro, L ;
Colombo, M ;
Rodés, J .
JOURNAL OF HEPATOLOGY, 2001, 35 (03) :421-430
[5]   Transarterial chemoembolization for unresectable hepatocellular carcinoma:: Meta-analysis of randomized controlled trials [J].
Cammà, C ;
Schepis, F ;
Orlando, A ;
Albanese, M ;
Shahied, L ;
Trevisani, F ;
Andreone, P ;
Craxì, A ;
Cottone, M .
RADIOLOGY, 2002, 224 (01) :47-54
[6]  
CHANG JM, 1994, CANCER, V74, P2449, DOI 10.1002/1097-0142(19941101)74:9<2449::AID-CNCR2820740910>3.0.CO
[7]  
2-4
[8]  
GERSCHWIND FH, 2002, J VASC INTERV RADIOL, V13, P1163
[9]   New intra-arterial drug delivery system for the treatment of liver cancer: Preclinical assessment in a rabbit model of liver cancer [J].
Hong, K ;
Khwaja, A ;
Liapi, E ;
Torbenson, MS ;
Georgiades, CS ;
Geschwind, JFH .
CLINICAL CANCER RESEARCH, 2006, 12 (08) :2563-2567
[10]  
Hotta N, 2003, HEPATO-GASTROENTEROL, V50, P1867