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首页> 外文期刊>OncoTargets and therapy >A pooled analysis of transarterial radioembolization with yttrium-90 microspheres for the treatment of unresectable intrahepatic cholangiocarcinoma
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A pooled analysis of transarterial radioembolization with yttrium-90 microspheres for the treatment of unresectable intrahepatic cholangiocarcinoma

机译:钇90微球经动脉放射栓塞治疗无法切除的肝内胆管癌的汇总分析

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Purpose: The aim of this pooled analysis was to evaluate the clinical efficacy and safety of transarterial radioembolization (TARE) with yttrium-90 (sup90/supY) microspheres for the treatment of unresectable intrahepatic cholangiocarcinoma (ICC). Methods: We searched the Cochrane Library, Embase, PubMed, SCI with the English language from inception to October 2018. A pooled analysis was conducted using Stata software. Results: There were 16 eligible studies included in this pooled analysis. The pooled median overall survival (OS) from 12 studies was 14.3 (95% CI: 11.9–17.1) months. Based on Response Evaluation Criteria in Solid Tumors (RECIST), no complete response was reported, and the median of partial response, stable disease and progressive disease were 11.5% (range: 4.8–35.3%), 61.5% (range: 42.9–81.3%) and 22.7% (range: 12.5–52.4%) respectively. The pooled disease control rate (DCR) from nine studies was 77.2% (95% CI: 70.2–84.2%). According to the type of microspheres, subgroup analysis was performed, the median OS in the glass microspheres group was 14.0 (95% CI: 9.1–21.4) months, and 14.3 (95% CI: 11.5–17.8) months in the resin microspheres group. The DCR was 77.3% (95% CI: 63.5–91.1%) and 77.4% (95% CI: 66.8–87.9%) in the glass and resin microspheres groups respectively. Most of the side effects reported in the included studies were mild and did not require intervention. Conclusion: TARE with sup90/supY microspheres is safe and effective for patients with unresectable ICC with acceptable side effects. And it seems that the type of microsphere has no influence on therapeutic efficacy.
机译:目的:本汇总分析的目的是评估钇90( 90 Y)微球经动脉放射栓塞(TARE)治疗不可切除的肝内胆管癌(ICC)的临床疗效和安全性。方法:从开始到2018年10月,我们用英语搜索Cochrane图书馆,Embase,PubMed,SCI。使用Stata软件进行汇总分析。结果:该汇总分析中包含16项合格研究。来自12项研究的汇总中位总体生存期(OS)为14.3个月(95%CI:11.9-17.1)。根据实体瘤反应评估标准(RECIST),没有完全反应的报道,部分反应,稳定疾病和进行性疾病的中位数分别为11.5%(范围:4.8–35.3%),61.5%(范围:42.9–81.3) %)和22.7%(范围:12.5–52.4%)。九项研究的综合疾病控制率(DCR)为77.2%(95%CI:70.2-84.2%)。根据微球的类型,进行了亚组分析,玻璃微球组的OS中位数为14.0(95%CI:9.1-21.4)个月,树脂微球组为14.3(95%CI:11.5-17.8)个月。 。在玻璃和树脂微球组中,DCR分别为77.3%(95%CI:63.5–91.1%)和77.4%(95%CI:66.8–87.9%)。纳入研究报告的大多数副作用是轻度的,不需要干预。结论:带有 90 Y微球的TARE对不能切除的ICC患者安全有效,且副作用可接受。而且似乎微球的类型对治疗功效没有影响。

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