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一项关于结直肠癌肝转移经动脉化疗栓塞术的多中心、国际、观察性研究:CIREL 的设计和原理。

A multicentre, international, observational study on transarterial chemoembolisation in colorectal cancer liver metastases: Design and rationale of CIREL.

机构信息

SLK-Kliniken Heilbronn GmbH, Klinik für Radiologie, Minimal-invasive Therapien und Nuklearmedizin, Am Gesundbrunnen 20-26, Heilbronn 74078, Germany.

Asklepios Tumorzentrum Hamburg, AK Altona, Oncology and Hematology, Paul-Ehrlich-Straße 1, 22763 Hamburg, Germany.

出版信息

Dig Liver Dis. 2020 Aug;52(8):857-861. doi: 10.1016/j.dld.2020.05.051. Epub 2020 Jun 30.

DOI:10.1016/j.dld.2020.05.051
PMID:
32620520
Abstract

BACKGROUND

About 70-80% of patients with colorectal liver metastases appear as ineligible for a curative treatment approach. Transarterial chemoembolisation (TACE) using irinotecan-eluting beads has emerged as a promising treatment option in cases with irresectable liver metastases. Despite being in clinical practice for years, little is known about the treatment characteristics and outcomes when used as per routine hospital practice.

METHODS

Patients with hepatic metastases from colorectal cancer origin, admitted to contributing centres to receive TACE with drug-eluting LifePearl® Microspheres loaded with irinotecan, as part of their standard care, will be consecutively added to the registry. Data will be collected until the end of study, loss to follow-up or death. Primary endpoint is the characterisation of the treatment usage at the selected sites in Europe. Secondary endpoints include outcome parameters, safety and toxicity, as well as quality of life.

CONCLUSION AND AIMS

This multicentre, international, prospective observational study conducted in European centres plans to collect real-life data. This data will form an evidence-base from which conclusions can be drawn on how to improve patient selection and optimise treatment protocols when treating with TACE using irinotecan-eluting microspheres. Trial registration NCT03086096.

摘要

背景

约 70-80%的结直肠癌肝转移患者被认为不适合根治性治疗方法。载有伊立替康的可载药微球经肝动脉化疗栓塞术(TACE)已成为不可切除肝转移灶的一种有前途的治疗选择。尽管 TACE 已在临床上应用多年,但对于按照常规医院实践使用 TACE 的治疗特征和结果却知之甚少。

方法

将来自结直肠癌肝转移的患者连续纳入本研究,这些患者因接受载有伊立替康的可载药 LifePearl®微球行 TACE 治疗作为其标准治疗而入住参与中心。将收集数据直至研究结束、随访丢失或死亡。主要终点是在选定的欧洲中心对 TACE 的治疗使用情况进行特征描述。次要终点包括结局参数、安全性和毒性以及生活质量。

结论和目的

这项在欧洲中心进行的多中心、国际、前瞻性观察性研究计划收集真实世界数据。该数据将为如何在使用载有伊立替康的微球进行 TACE 治疗时改善患者选择和优化治疗方案提供依据。试验注册 NCT03086096。

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引用本文的文献

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ESMO Open. 2025 Mar;10(3):104292. doi: 10.1016/j.esmoop.2025.104292. Epub 2025 Feb 15.
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Safety, Feasibility and Technical Considerations from a Prospective, Observational Study-CIREL: Irinotecan-TACE for CRLM in 152 Patients.一项前瞻性观察性研究——CIREL的安全性、可行性及技术考量:152例接受伊立替康经动脉化疗栓塞术治疗的结直肠癌肝转移患者
J Clin Med. 2022 Oct 19;11(20):6178. doi: 10.3390/jcm11206178.
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Cardiovasc Intervent Radiol. 2022 Jun;45(6):770-779. doi: 10.1007/s00270-021-03039-1. Epub 2022 Jan 14.