医学
肝细胞癌
阿霉素
临床终点
射频消融术
置信区间
内科学
吉西他滨
泌尿科
靶病变
代理终结点
人口
无进展生存期
胃肠病学
肿瘤科
化疗
外科
烧蚀
随机对照试验
心肌梗塞
经皮冠状动脉介入治疗
环境卫生
作者
Won Young Tak,Shi-Ming Lin,Yijun Wang,Jiasheng Zheng,Aldo Vecchione,Soo Young Park,Minhua Chen,Stephen N. Wong,Ruocai Xu,Cheng‐Yuan Peng,Yi‐You Chiou,Guan‐Tarn Huang,Jianqiang Cai,Basri Johan Jeet Abdullah,June Sung Lee,Jae Young Lee,Jongyoung Choi,Julieta Gopez-Cervantes,Morris Sherman,Richard S. Finn
标识
DOI:10.1158/1078-0432.ccr-16-2433
摘要
Abstract Purpose: Lyso-thermosensitive liposomal doxorubicin (LTLD) consists of doxorubicin contained within a heat-sensitive liposome. When heated to ≥40°C, LTLD locally releases a high concentration of doxorubicin. We aimed to determine whether adding LTLD improves the efficacy of radiofrequency ablation (RFA) for hepatocellular carcinoma (HCC) lesions with a maximum diameter (dmax) of 3 to 7 cm. Experimental Design: The HEAT Study was a randomized, double-blind, dummy-controlled trial of RFA ± LTLD. The 701 enrolled patients had to have ≤4 unresectable HCC lesions, at least one of which had a dmax of 3 to 7 cm. The primary endpoint was progression-free survival (PFS) and a key secondary endpoint was overall survival (OS). Post hoc subset analyses investigated whether RFA duration was associated with efficacy. Results: The primary endpoint was not met; in intention-to-treat analysis, the PFS HR of RFA + LTLD versus RFA alone was 0.96 [95% confidence interval (CI), 0.79-1.18; P = 0.71], and the OS HR ratio was 0.95 (95% CI, 0.76–1.20; P = 0.67). Among 285 patients with a solitary HCC lesion who received ≥45 minutes RFA dwell time, the OS HR was 0.63 (95% CI, 0.41–0.96; P < 0.05) in favor of combination therapy. RFA + LTLD had reversible myelosuppression similar to free doxorubicin. Conclusions: Adding LTLD to RFA was safe but did not increase PFS or OS in the overall study population. However, consistent with LTLD's heat-based mechanism of action, subgroup analysis suggested that RFA + LTLD efficacy is improved when RFA dwell time for a solitary lesion ≥45 minutes. Clin Cancer Res; 24(1); 73–83. ©2017 AACR.
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