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首页> 外文期刊>Journal of Gastrointestinal Oncology >Radioembolization with 90 Y glass microspheres for the treatment of unresectable metastatic liver disease from chemotherapy-refractory gastrointestinal cancers: final report of a prospective pilot study
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Radioembolization with 90 Y glass microspheres for the treatment of unresectable metastatic liver disease from chemotherapy-refractory gastrointestinal cancers: final report of a prospective pilot study

机译:90 Y玻璃微球体的放射栓塞治疗无法治愈的化疗难治性胃肠道癌转移性肝病:一项前瞻性试验研究的最终报告

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Background: This prospective pilot single-institution study was undertaken to document the feasibility, safety, and efficacy of radioembolization of liver-dominant metastatic gastrointestinal cancer using 90 Y glass microspheres. Methods: Between June 2010 and October 2013, 42 adult patients (26 men, 16 women; median age 60 years) with metastatic chemotherapy-refractory unresectable colorectal (n=21), neuroendocrine (n=11), intrahepatic bile duct (n=7), pancreas (n=2), and esophageal (n=1) carcinomas underwent 60 lobar or segmental administrations of 90 Y glass microspheres. Data regarding clinical and laboratory adverse events (AE) were collected prospectively for up to 5.5 years after radioembolization. Radiographic responses were evaluated using Response Evaluation Criteria in Solid Tumors (RECIST), version 1.1. Time to maximum response, response duration, progression-free survival (PFS) (hepatic and extrahepatic), and overall survival (OS) were measured. Results: Median target dose and activity were 109.4 Gy and 2.6 GBq per treatment session, respectively. Majority of clinical AE were grade 1 or 2 in severity. Patients with colorectal cancer had hepatic objective response rate (ORR) of 25% and a hepatic disease control rate (DCR) of 80%. Median PFS and OS were 1.0 and 4.4 months, respectively. Patients with neuroendocrine tumors (NET) had hepatic ORR and DCR of 73% and 100%, respectively. Median PFS was 8.9 months for this cohort. DCR and median PFS and OS for patients with cholangiocarcinoma were 86%, 1.1 months, and 6.7 months, respectively. Conclusions: 90 Y glass microspheres device has a favorable safety profile, and achieved prolonged disease control of hepatic tumor burden in a subset of patients, including all patients enrolled in the neuroendocrine cohort.
机译:背景:这项前瞻性的单机构先导研究旨在证明使用90 Y玻璃微球体进行以肝为主的转移性胃肠道癌的放射栓塞的可行性,安全性和有效性。方法:2010年6月至2013年10月之间,有42例成年患者(男26例,女16例;中位年龄60岁),接受转移性化疗-难治性不可切除结直肠癌(n = 21),神经内分泌(n = 11),肝内胆管(n = 7),胰腺(n = 2)和食管癌(n = 1)接受了60个大叶或90 Y玻璃微球的分段给药。放射栓塞后长达5.5年的前瞻性收集了有关临床和实验室不良事件(AE)的数据。使用实体肿瘤缓解评估标准(RECIST)1.1版评估放射线反应。测量了达到最大反应的时间,反应持续时间,无进展生存期(PFS)(肝和肝外)和总生存期(OS)。结果:每疗程中位靶剂量和活性分别为109.4 Gy和2.6 GBq。临床AE的严重程度为1级或2级。大肠癌患者的肝客观反应率(ORR)为25%,肝病控制率(DCR)为80%。 PFS和OS的中位数分别为1.0个月和4.4个月。神经内分泌肿瘤(NET)患者的肝ORR和DCR分别为73%和100%。该队列的中位PFS为8.9个月。胆管癌患者的DCR和中位PFS和OS分别为86%,1.1个月和6.7个月。结论:90 Y玻璃微球装置具有良好的安全性,并在部分患者(包括所有参加神经内分泌队列研究的患者)中实现了对肝脏肿瘤负担的长期疾病控制。

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