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用于孤立性肝细胞癌肿瘤的药物洗脱微球-TACE治疗患者的端孔与微阀输注导管:一项回顾性分析

End-hole Versus Microvalve Infusion Catheters in Patients Undergoing Drug-Eluting Microspheres-TACE for Solitary Hepatocellular Carcinoma Tumors: A Retrospective Analysis.

作者信息

Titano Joseph J, Fischman Aaron M, Cherian Arnav, Tully Madeline, Stein Lance L, Jacobs Louis, Rubin Raymond A, Bosley Michael, Citron Steve, Joelson Dean W, Shrestha Roshan, Arepally Aravind

机构信息

Department of Interventional Radiology, Mount Sinai, New York, NY, USA.

Transplant Institute, Piedmont Healthcare, Atlanta, GA, USA.

出版信息

Cardiovasc Intervent Radiol. 2019 Apr;42(4):560-568. doi: 10.1007/s00270-018-2150-6. Epub 2019 Jan 11.

DOI:10.1007/s00270-018-2150-6
PMID:30635728
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6394778/
Abstract

INTRODUCTION

Pre-transplant locoregional therapy for hepatocellular carcinoma (HCC) during bridge-to-transplant impacts recurrence and survival rates following liver transplantation. Optimizing the effectiveness of transarterial chemoembolization (TACE) in this population is imperative, and microvalve infusion catheters offer a means of such improvement.

METHODS

All treatment-naive patients with solitary HCC tumors < 6.5 cm who underwent drug-eluting microspheres (DEM) TACE between 04/2015 and 08/2017 were retrospectively reviewed. Eighty-eight included patients underwent DEM-TACE with either standard end-hole catheters (EH) or microvalve infusion catheters (MVI). The EH (n = 70) and MVI (n = 18) cohorts had similar baseline tumor size, laboratory values, and tumor etiologies.

RESULTS

Initial objective response rates were significantly higher in MVI vs. EH (100% vs. 76.5%, p = 0.019). There was no difference in adverse events between groups (p = 0.265). MVI patients exhibited lower AST (p = 0.003) and ALT (p = 0.044) at 6 months. Blinded pathological analysis of explanted livers showed greater concentrations of microspheres within the tumor relative to the surrounding tissue in MVI explants (88.7 ± 10.6%) versus the EH explants (55.3 ± 32.7%) (p = 0.002). There was significantly higher percentage tumor necrosis in the MVI group (89.0 ± 2.2%) compared with the EH group (56.1 ± 44.5%) (p = 0.006).

CONCLUSION

In this retrospective study of a single-center cohort, DEM-TACE procedures with MVI were associated with improved tumor response, increased deposition of microspheres within tumor tissue, and higher percentage tumor necrosis at explant relative to those performed using EH catheters.

摘要

引言

肝移植桥接治疗期间,肝细胞癌(HCC)的移植前局部区域治疗会影响肝移植后的复发率和生存率。优化该人群经动脉化疗栓塞术(TACE)的疗效至关重要,微阀输注导管提供了一种改善方法。

方法

回顾性分析2015年4月至2017年8月间所有接受药物洗脱微球(DEM)TACE治疗的初治孤立性HCC肿瘤患者,肿瘤直径<6.5cm。纳入的88例患者接受了DEM-TACE治疗,使用的是标准端孔导管(EH)或微阀输注导管(MVI)。EH组(n = 70)和MVI组(n = 18)在基线肿瘤大小、实验室检查值和肿瘤病因方面相似。

结果

MVI组的初始客观缓解率显著高于EH组(100%对76.5%,p = 0.019)。两组间不良事件无差异(p = 0.265)。MVI组患者在6个月时AST(p = 0.003)和ALT(p = 0.044)较低。对移植肝脏的盲法病理分析显示,MVI组移植肝脏肿瘤内微球浓度相对于周围组织高于EH组移植肝脏(分别为88.7±10.6%和55.3±32.7%)(p = 0.002)。MVI组肿瘤坏死百分比显著高于EH组(分别为89.0±2.2%和56.1±44.5%)(p = 0.006)。

结论

在这项单中心队列的回顾性研究中,与使用EH导管进行的DEM-TACE手术相比,使用MVI进行的DEM-TACE手术与更好的肿瘤反应、肿瘤组织内微球沉积增加以及移植时更高的肿瘤坏死百分比相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2305/6394778/794ec94c731e/270_2018_2150_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2305/6394778/9661ebe87678/270_2018_2150_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2305/6394778/cd2bbc7f1916/270_2018_2150_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2305/6394778/058eed650fd4/270_2018_2150_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2305/6394778/af7a8e6d2aeb/270_2018_2150_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2305/6394778/3ed233de5702/270_2018_2150_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2305/6394778/794ec94c731e/270_2018_2150_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2305/6394778/9661ebe87678/270_2018_2150_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2305/6394778/cd2bbc7f1916/270_2018_2150_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2305/6394778/058eed650fd4/270_2018_2150_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2305/6394778/af7a8e6d2aeb/270_2018_2150_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2305/6394778/3ed233de5702/270_2018_2150_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2305/6394778/794ec94c731e/270_2018_2150_Fig6_HTML.jpg

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