药代动力学
医学
阿霉素
肝细胞癌
药品
化疗
内科学
药理学
肿瘤科
作者
Marı́a Varela,María Isabel Real,Marta Burrel,Alejandro Forner,María Sala,Mercé Brunet,Carmen Ayuso,Lluı́s Castells,Xavier Montañá,Josep M. Llovet,Jordi Bruix
标识
DOI:10.1016/j.jhep.2006.10.020
摘要
Background/Aims
This study assesses the safety, pharmacokinetics and efficacy of transarterial chemoembolization using drug eluting beads (DEB), an embolizing device that slowly releases chemotherapy to decrease systemic toxicity. Methods
Twenty-seven Child-Pugh A cirrhotics (76% male, 59% HCV) with untreated large/multifocal HCC received chemoembolization with doxorubicin loaded DEBs at doses adjusted for bilirubin and body surface (range: 47–150mg). Clinical and analytical data were recorded at 24 and 48h, 7, 14 and 30days after first and second TACE. Response rate was assessed by CT at 6months. Blood samples were obtained in 13 patients at 5, 20, 40, 60, 120min, 6, 24, 48 and 168h to determine doxorubicin Cmax and AUC. Results
DEB-TACE was well tolerated with an acceptable safety profile. Two cases developed liver abscess, one leading to death. Response rate was 75% (66.6% on intention-to-treat). Doxorubicin Cmax and AUC were significantly lower in DEB-TACE patients (78.97±38.3ng/mL and 662.6±417.6ng/mLmin) than in conventional TACE (2341.5±3951.9ng/mL and 1812.2±1093.7ng/mLmin, p=0.00002 and p=0.001, respectively). After a median follow-up of 27.6months, 1- and 2-year survival is 92.5% and 88.9%, respectively. Conclusions
Chemoembolization using DEBs is an effective procedure with a favorable pharmacokinetic profile.
科研通智能强力驱动
Strongly Powered by AbleSci AI