Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania; Corporal Michael J. Crescenz VA Medical Center, 3900 Woodland Avenue, Bldg 21, Room A422, Philadelphia, PA 19014.
Yale University School of Medicine, New Haven, Connecticut; VA Connecticut Healthcare System, West Haven, Connecticut.
J Vasc Interv Radiol. 2018 Apr;29(4):540-549.e4. doi: 10.1016/j.jvir.2017.11.033. Epub 2018 Feb 22.
The impact of transarterial chemoembolization after initiation of sorafenib (SOR) has not been prospectively compared with SOR alone in unresectable hepatocellular carcinoma (HCC). The objective of this study was to assess whether SOR + transarterial chemoembolization provides benefit over SOR alone in this setting.
A retrospective cohort study with propensity matching using data from patients prescribed SOR for HCC at Veterans Health Administration hospitals from 2007 to 2015. The primary outcome was overall survival from the time of SOR prescription and stratified by receipt of transarterial chemoembolization within 90 days of SOR initiation.
A total of 4,896 patients received SOR for HCC, of whom 232 (4.7%) underwent transarterial chemoembolization within 90 days. Patients receiving transarterial chemoembolization + SOR were highly selected, being younger and with less significant hepatic dysfunction, earlier Barcelona Clinic Liver Cancer stage (P < .0001), and fewer tumors with lower rates of macrovascular invasion (MVI) and metastases (all P < .0001) than SOR-alone patients. In unadjusted analysis, SOR + transarterial chemoembolization was associated with reduced mortality (hazard ratio [HR] 0.61, 95% confidence interval [CI] 0.53-0.71; P < .0001). After propensity matching, SOR + transarterial chemoembolization continued to show significant associations with reduced mortality with HR 0.75 (95% CI 0.62-0.92; P = .0005). Subgroup analysis suggests that the addition of transarterial chemoembolization to SOR improves outcomes in most patients, particularly those with Model for End-Stage Liver Disease score <15, platelets >50,000/μL, and >3 tumors with or without macrovascular invasion, without local invasion or metastases.
Patients with unresectable HCC started on systemic therapy with SOR appear to benefit from adjuvant transarterial chemoembolization. Optimal application of multimodal therapy in this setting should be prospectively investigated.
在不可切除的肝细胞癌(HCC)患者中,经动脉化疗栓塞(TACE)联合索拉非尼(SOR)的疗效尚未与单纯 SOR 进行前瞻性比较。本研究旨在评估在这种情况下,SOR+TACE 是否优于单纯 SOR。
采用回顾性队列研究,对 2007 年至 2015 年期间在退伍军人健康管理局医院接受 SOR 治疗 HCC 的患者数据进行倾向评分匹配。主要终点是从 SOR 处方开始的时间至 SOR 开始后 90 天内接受 TACE 的总生存时间,并进行分层分析。
共有 4896 例患者接受 SOR 治疗 HCC,其中 232 例(4.7%)在 SOR 开始后 90 天内行 TACE。接受 TACE+SOR 的患者选择度较高,他们年龄较小,肝功能障碍较轻,巴塞罗那临床肝癌分期较早(P<0.0001),肿瘤数目较少,大血管侵犯(MVI)和转移率较低(均 P<0.0001)。未校正分析显示,SOR+TACE 治疗与死亡率降低相关(风险比[HR] 0.61,95%置信区间[CI] 0.53-0.71;P<0.0001)。经倾向评分匹配后,SOR+TACE 治疗仍与死亡率降低显著相关,HR 为 0.75(95% CI 0.62-0.92;P=0.0005)。亚组分析表明,在大多数患者中,TACE 联合 SOR 治疗可改善预后,特别是 MELD 评分<15、血小板>50,000/μL、肿瘤>3 个且无或有 MVI、无局部侵犯或转移的患者。
接受 SOR 系统治疗的不可切除 HCC 患者似乎受益于辅助 TACE。应前瞻性研究这种情况下的多模式治疗的最佳应用。