Chai Weilu, Zhao Qiyu, Kong Dexing, Jiang Tian'an
Department of Ultrasonography, The First Affiliated Hospital, College of Medicine, Zhejiang University, #79 Qingchun Road, Hangzhou, Zhejiang, 310003, P.R. China.
Department of Hepatobiliary and Pancreatic Surgery, The First Affiliated Hospital, College of Medicine, Zhejiang University, #79 Qingchun Road, Hangzhou, Zhejiang, 310003, P.R. China.
Lasers Surg Med. 2019 Dec;51(10):866-873. doi: 10.1002/lsm.23123. Epub 2019 Jul 8.
Limited data have been used to evaluate the feasibility and effectiveness of percutaneous laser ablation (PLA) (a modality that has been proven to be a safe method for tumors in high-risk locations) for hepatic tumors in the space between the portal vein and inferior vena cava (IVC). The goal of this study was to investigate the characteristics and therapeutic effectiveness of ultrasound-guided PLA of hepatic tumors in the portacaval space.
STUDY DESIGN/MATERIALS AND METHODS: Ten patients, who had hepatic tumors in the portacaval space (defined as tumors located in the space formed by the hepatic portal vein and IVC less than 5 mm from the margins of both vessels), receiving ultrasound-guided PLA between January 2016 and June 2017 were analyzed. Tumors in the type I portacaval space were enclosed on three sides of major vessels, and tumors in the type II portacaval space were enclosed on two sides of major vessels. The technical success, treatment response, complete tumor ablation (CTA), local tumor progression (LTP), and distant tumor recurrence (DTR) were assessed and recorded at the follow-up.
The mean tumor diameter was 1.8 ± 0.4 cm. Technical success and initial CTA were achieved in all 10 patients without major complications. The 6-month and 12-month LTP rates were 0% and 10%, respectively. The DTR rate was 20% at both the 6- and 12-month follow-ups.
The preliminary results showed that ultrasound-guided PLA was feasible and safe for tumors in the portacaval space, and further studies on larger populations with a longer follow-up are needed to delineate the use of PLA and evaluate its therapeutic efficacy. Lasers Surg. Med. © 2019 Wiley Periodicals, Inc.
用于评估经皮激光消融术(PLA)(一种已被证明对高危部位肿瘤安全的治疗方式)治疗门静脉与下腔静脉(IVC)之间肝肿瘤的可行性和有效性的数据有限。本研究的目的是探讨超声引导下经皮激光消融术治疗门腔间隙肝肿瘤的特点和治疗效果。
研究设计/材料与方法:分析2016年1月至2017年6月期间接受超声引导下经皮激光消融术的10例门腔间隙肝肿瘤患者(定义为位于肝门静脉和下腔静脉形成的间隙内、距两血管边缘小于5mm的肿瘤)。I型门腔间隙肿瘤被主要血管包围三面,II型门腔间隙肿瘤被主要血管包围两面。在随访时评估并记录技术成功率、治疗反应、完全肿瘤消融(CTA)、局部肿瘤进展(LTP)和远处肿瘤复发(DTR)。
平均肿瘤直径为1.8±0.4cm。所有10例患者均获得技术成功和初始CTA,无重大并发症。6个月和12个月的LTP率分别为0%和10%。6个月和12个月随访时的DTR率均为20%。
初步结果表明,超声引导下经皮激光消融术治疗门腔间隙肿瘤是可行且安全的,需要对更多人群进行更长时间的随访研究,以明确经皮激光消融术的应用并评估其治疗效果。激光外科与医学杂志。©2019威利期刊公司。