Department of Radiology, Chung-Ang University Gwangmyeong Hospital, Chung-Ang University College of Medicine, Gwangmyeong, Korea.
Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Eur J Radiol. 2024 Jun;175:111446. doi: 10.1016/j.ejrad.2024.111446. Epub 2024 Mar 25.
To investigate the safety and efficacy of large-bore uncovered stents for treating malignant superior vena cava syndrome.
This retrospective study included 115 patients (89 men, 26 women; mean age 63.2 years; range 21-83 years) who underwent endovascular large-bore (≥18 mm in diameter) uncovered stent placement between August 2015 and July 2022. One patient was lost to follow-up. Therefore, 114 patients were available for follow-up.
Stent placement was technically successful in all 115 patients. Minor procedure-related complications occurred in nine (7.8 %) patients. One hundred eight (93.9 %) patients experienced complete or marked symptomatic relief (Kishi score ≤ 2) at a mean of 3 days after procedure. The cumulative stent patency rates were 98.2 %, 95 %, 93.7 %, 91.5 %, 83.5 %, and 83.5 % at 1, 3, 6, 12, 18, and 24 months, respectively. Stent occlusion occurred in ten (8.8 %) of 114 patients at a mean of 215 days (range 1-732 days) due to thrombosis (n = 7) and tumor ingrowth (n = 3). Stent occlusion did not occur in 21 patients who underwent subsequent central venous catheter insertion. The median patient survival time was 159 days (95 % confidence interval 102-216 days). Univariate and multivariate Cox regression analysis revealed adjuvant anticancer treatment (p = 0.001) and tumor response (p < 0.001) as independent predictors of patient survival.
Endovascular placement of large-bore uncovered stents was a safe and effective treatment for malignant superior vena cava syndrome. Large-bore stent placement can effectively prevent stent occlusion by tumor ingrowth in most cases, and it can provide a sufficient diameter for subsequent insertion of central venous catheters.
探讨大口径无覆膜支架治疗恶性上腔静脉综合征的安全性和疗效。
本回顾性研究纳入了 2015 年 8 月至 2022 年 7 月期间 115 例(89 例男性,26 例女性;平均年龄 63.2 岁;范围 21-83 岁)接受血管内大口径(≥18mm 直径)无覆膜支架置入的患者。1 例患者失访。因此,114 例患者可进行随访。
115 例患者支架置入技术均成功。9 例(7.8%)患者发生轻微的手术相关并发症。108 例(93.9%)患者在术后平均 3 天(Kishi 评分≤2)时症状完全或明显缓解。支架通畅率分别为 1 个月时 98.2%、3 个月时 95%、6 个月时 93.7%、12 个月时 91.5%、18 个月时 83.5%和 24 个月时 83.5%。114 例患者中有 10 例(8.8%)在平均 215 天(范围 1-732 天)后因血栓形成(n=7)和肿瘤内生长(n=3)发生支架闭塞。21 例随后行中心静脉导管插入术的患者未发生支架闭塞。中位患者生存时间为 159 天(95%置信区间 102-216 天)。单因素和多因素 Cox 回归分析显示,辅助抗癌治疗(p=0.001)和肿瘤反应(p<0.001)是患者生存的独立预测因素。
血管内放置大口径无覆膜支架治疗恶性上腔静脉综合征是一种安全有效的方法。大口径支架置入术可有效防止大多数情况下肿瘤内生长引起的支架闭塞,并且可为随后插入中心静脉导管提供足够的直径。