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兔肝癌模型中经动脉司维拉姆栓塞术的安全性和有效性评估:对血管闭塞大小规则的挑战

Evaluation of the safety and efficacy of transarterial sevelamer embolization in a rabbit liver cancer model: A challenge on the size rule for vascular occlusion.

作者信息

Chen Hong, Xie Chuan-Sheng, Li Yan-Shu, Deng Zhi-Qiang, Lv Yang-Feng, Bi Qiu-Chen, Tang Jian-Jun, Luo Rong-Guang, Tang Qun

机构信息

Jiangxi Provincial Key Laboratory of Preventive Medicine, School of Public Health, Nanchang University, Nanchang, China.

Jiangxi Center of Medical Device Testing, Nanchang, China.

出版信息

Front Bioeng Biotechnol. 2022 Dec 12;10:1058042. doi: 10.3389/fbioe.2022.1058042. eCollection 2022.

Abstract

As the most efficient method to treat hepatocellular carcinoma in the immediate or advanced stage, transarterial chemoembolization (TACE) is coming into the era of microsphere (MP). Drug-eluting beads have shown their huge potential as an embolic agent and drug carrier for chemoembolization, but their sizes are strictly limited to be above 40 μm, which was considered to occlude vessels in a safe mode. microsphere smaller than 40 µm is easy to be washed out and transported to the normal liver lobe or other organs, causing severe adverse events and failed embolization. To determine whether sevelamer ultrafine particle (0.2-0.5 µm) is qualified as a safe and efficient embolic agent, we investigated the safety and therapeutic efficiency of transarterial sevelamer embolization (TASE) in the VX2 rabbit liver cancer model, aiming to challenge the "40 µm" rule on the selection criteria of the MP. In a four-arm study, blank bead (Callisphere, 100-300 µm), luminescent polystyrene microsphere (10, 100 µm), and sevelamer particle were transarterially administered to evaluate the threshold size of the MP size for intrahepatic or extrahepatic permeability. Another four-arm study was designed to clarify the safety and efficiency of preclinical transarterial sevelamer embolizationTASE tests over other techniques. Sham (saline), TASE, C-TACE, and D-TACE ( = 6) were compared in terms of serum chemistry, histopathology, and tumor necrosis ratio. In the first trials, the "40 µm" rule was detectable on the VX2 cancer model, but the regulation has no application to the new embolic agent as sevelamer ultrafine particles have not been found to leak out from the VX2 lesions, only found in the embolized vessels. Pathology proves that less viable tumor residue was found 2 weeks after the procedure, evidencing a better therapeutic outcome. No adverse events were found except for a short stress response. These results indicate that sevelamer is a safe and efficient embolic as an alternative to the current MP-based embolization therapy techniques.

摘要

作为治疗早期或晚期肝细胞癌的最有效方法,经动脉化疗栓塞术(TACE)正步入微球(MP)时代。载药微球已显示出其作为化疗栓塞术的栓塞剂和药物载体的巨大潜力,但其尺寸严格限制在40μm以上,这被认为是以安全模式阻塞血管。小于40μm的微球容易被冲走并输送到正常肝叶或其他器官,导致严重不良事件和栓塞失败。为了确定司维拉姆超细颗粒(0.2 - 0.5μm)是否符合安全有效的栓塞剂标准,我们在VX2兔肝癌模型中研究了经动脉司维拉姆栓塞术(TASE)的安全性和治疗效果,旨在挑战MP选择标准中的“40μm”规则。在一项四臂研究中,经动脉给予空白微球(Callisphere,100 - 300μm)、发光聚苯乙烯微球(10、100μm)和司维拉姆颗粒,以评估MP尺寸对肝内或肝外通透性的阈值大小。另一项四臂研究旨在阐明临床前经动脉司维拉姆栓塞术(TASE)试验相对于其他技术的安全性和有效性。在血清化学、组织病理学和肿瘤坏死率方面比较了假手术(生理盐水)、TASE、C-TACE和D-TACE(每组n = 6)。在首次试验中,在VX2癌症模型上可检测到“40μm”规则,但该规则不适用于新的栓塞剂,因为未发现司维拉姆超细颗粒从VX2病变中漏出,仅在栓塞血管中发现。病理学证明术后2周发现存活肿瘤残留较少,证明治疗效果更好。除了短暂的应激反应外,未发现不良事件。这些结果表明,司维拉姆作为一种栓塞剂是安全有效的,可替代当前基于MP的栓塞治疗技术。

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