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经肝动脉化疗栓塞术联合 DC Bead LUMI™显影微球治疗原发性肝癌:初步经验。

Transarterial chemoembolization with DC Bead LUMI™ radiopaque beads for primary liver cancer treatment: preliminary experience.

机构信息

Oncology Radiodiagnostics Department, Oncology Institute of Veneto, Institute for the Research & Treatment of Cancer (IRCC), 35128 Padova, Italy.

Onco-Ematology Department, Azienda Ospedaliera 'Ospedali Riuniti Marche Nord', 61122 Pesaro, Italy.

出版信息

Future Oncol. 2017 Oct;13(25):2243-2252. doi: 10.2217/fon-2017-0364. Epub 2017 Oct 24.

Abstract

AIM

Primary objectives of the study were to assess the safety of transarterial chemoembolization (TACE) using DC Bead LUMI™ for the treatment of hepatocellular carcinoma and beads distribution after TACE.

PATIENTS/METHODS: This was a prospective observational cohort study. The study included 44 hepatocellular carcinoma patients who were treated with TACE using DC Bead LUMI. Beads distribution was monitored 1 h after TACE by CT scan.

RESULTS

TACE had no intraprocedural complications. Observed side effects were of mild intensity and included pain in 5 (11%), fever in 4 (9%) and vomiting in 2 (5%) patients. Most patients (89%) reported no adverse event. Non-target distribution was observed in only two cases (5%).

CONCLUSION

DC Bead LUMI allowed assessing in real time their distribution. This could prevent non-target infusion and reduce toxicity.

摘要

目的

本研究的主要目的是评估使用 DC Bead LUMI™进行经动脉化疗栓塞(TACE)治疗肝细胞癌的安全性和 TACE 后微球的分布情况。

患者/方法:这是一项前瞻性观察性队列研究。研究纳入了 44 例接受 DC Bead LUMI 进行 TACE 治疗的肝细胞癌患者。在 TACE 后 1 小时通过 CT 扫描监测微球的分布情况。

结果

TACE 无术中并发症。观察到的副作用为轻度,包括 5 例(11%)疼痛、4 例(9%)发热和 2 例(5%)呕吐。大多数患者(89%)无不良事件报告。只有 2 例(5%)观察到非靶区分布。

结论

DC Bead LUMI 允许实时评估其分布情况。这可以防止非靶区输注并降低毒性。

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