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⁹⁰Y 微球经动脉内治疗肝细胞癌:根特大学医院 4 年经验。

Intra-arterial treatment with ⁹⁰Y microspheres for hepatocellular carcinoma: 4 years experience at the Ghent University Hospital.

机构信息

Department of Nuclear Medicine, Ghent University Hospital, De Pintelaan 185, 9000 Ghent, Belgium.

出版信息

Eur J Nucl Med Mol Imaging. 2011 Dec;38(12):2117-24. doi: 10.1007/s00259-011-1881-2. Epub 2011 Jul 27.

Abstract

PURPOSE

We report on our experience in terms of eligibility, safety, response and survival for treatment of hepatocellular carcinoma (HCC) with (90)Y microspheres. Secondly, we investigated the urinary excretion of (90)Y following treatment.

METHODS

We retrospectively reviewed all HCC patients referred to our department for (90)Y microsphere treatment. We recorded reasons for not proceeding to actual treatment. In case treatment was performed, we assessed the tolerance (Common Terminology Criteria for Adverse Events v3.0, CTCAE v3.0), the response [modified Response Evaluation Criteria in Solid Tumors (mRECIST) criteria] and long-term survival (Kaplan-Meier). The urinary excretion was estimated by 12-h urine collections post-injection for analysis in a gamma counter.

RESULTS

Forty-three HCC patients were referred for radioembolization. Fourteen patients were excluded, mainly due to unfavourable (99m)Tc-macroaggregated albumin (MAA) distribution. Twenty-nine patients were treated with (90)Y microspheres (TheraSphere, mean activity 2.17 GBq). In four patients severe clinical adverse events were encountered, however only in one case clearly related to the therapy. Twenty patients were assessable by mRECIST: complete response in 15%, partial response in 35%, stable disease in 30% and progression in 20% were observed. A median survival of 12.3 months (95% confidence interval 9.4-15.2) was estimated. Concerning the substudy on urinary excretion, only 0.0025% of the administered activity was excreted in the urine within the first 12 h following TheraSphere.

CONCLUSION

Following a strict workup before admitting patients to radioembolization with TheraSphere, we found good clinical tolerance in the vast majority of patients. Radiological response assessment yielded an overall response rate of 50%, when evaluated early following treatment. Urine analysis showed consistently only low activities of (90)Y excreted in the urine.

摘要

目的

我们报告了使用(90)Y 微球治疗肝细胞癌(HCC)的入选标准、安全性、疗效和生存情况。其次,我们研究了治疗后(90)Y 的尿排泄情况。

方法

我们回顾性分析了所有因接受(90)Y 微球治疗而转至我科的 HCC 患者。我们记录了未进行实际治疗的原因。如果进行了治疗,则评估治疗的耐受性(不良事件通用术语标准第 3.0 版,CTCAE v3.0)、疗效[改良实体瘤反应评价标准(mRECIST)]和长期生存(Kaplan-Meier)。通过注射后 12 小时的尿液收集进行分析,用γ计数器估计尿排泄量。

结果

43 例 HCC 患者被转介进行放射性栓塞治疗。14 例患者被排除在外,主要是由于(99m)Tc-聚合白蛋白(MAA)分布不佳。29 例患者接受了(90)Y 微球治疗(TheraSphere,平均活度 2.17GBq)。4 例患者出现严重的临床不良事件,但只有 1 例与治疗明显相关。20 例患者可通过 mRECIST 进行评估:完全缓解 15%,部分缓解 35%,稳定疾病 30%,进展 20%。中位生存时间估计为 12.3 个月(95%置信区间 9.4-15.2)。关于尿排泄的子研究,TheraSphere 治疗后 12 小时内仅 0.0025%的给药活度排泄到尿液中。

结论

在对接受 TheraSphere 放射性栓塞治疗的患者进行严格的筛选后,我们发现绝大多数患者的临床耐受性良好。早期治疗后,放射学反应评估的总体反应率为 50%。尿液分析显示(90)Y 的活性始终较低。

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