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首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >Randomised trial of SIR-Spheres plus chemotherapy vs. chemotherapy alone for treating patients with liver metastases from primary large bowel cancer.
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Randomised trial of SIR-Spheres plus chemotherapy vs. chemotherapy alone for treating patients with liver metastases from primary large bowel cancer.

机译:SIR-Spheres联合化学疗法与单纯化学疗法治疗原发性大肠癌肝转移患者的随机试验。

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摘要

PURPOSE: SIR-Spheres are radioactive yttrium90 microspheres (SIR-Spheres, Sirtex Medical Limited, Australia) used to selectively target high levels of ionising radiation to tumors within the liver. This trial was designed to measure any increased patient benefit by adding a single administration of SIR-Spheres to a regimen of regional hepatic artery chemotherapy (HAC) administered as a 12 day infusion of floxuridine and repeated at monthly intervals, vs. the same chemotherapy alone. PATIENTS AND METHODS: A phase III randomised clinical trial entering 74 patients was undertaken on patients with bi-lobar non-resectable liver metastases from primary adenocarcinoma of the large bowel. Patient benefit criteria assessed in the trial were tumor response, time to disease progression in the liver, overall survival, quality of life, and treatment related toxicity. Tumor response was measured by serial changes in both cross-sectional tumor areas and total tumor volumes, provided any response lasted not less than three months as well as changes in serum carcino-embryonic antigen (CEA). RESULTS: The partial and complete response rate (PR + CR) was significantly greater for patients receiving SIR-Spheres when measured by tumor areas (44%) vs. 17.6%, P = 0.01) tumor volumes (50% vs. 24%, P = 0.03) and CEA (72% vs. 47%, P = 0.004). The median time to disease progression in the liver was significantly longer for patients receiving SIR-Spheres in comparison to patients receiving HAC alone when measured by either tumor areas (9.7 vs. 15.9 months, P = 0.001), tumor volumes (7.6 vs. 12.0 months, P = 0.04) or CEA (5.7 vs. 6.7 months, P = 0.06). The one, two, three and five-year survival for patients receiving SIR-Spheres was 72%, 39%, 17% and 3.5%, compared to 68%, 29%, 6.5% and 0% for HAC alone. Cox regression analysis suggests an improvement in survival for patients treated with SIR-Spheres who survive more than 15 months (P = 0.06). There was no increase in grade 3-4 treatment related toxicity and no loss of quality of life for patients receiving SIR-Spheres in comparison to patients receiving HAC alone. CONCLUSION: The combination of a single injection of SIR-Spheres plus HAC is substantially more effective in increasing tumor responses and progression free survival than the same regimen of HAC alone.
机译:目的:SIR-Spheres是放射性钇90微球(SIR-Spheres,Sirtex Medical Limited,澳大利亚),用于选择性地将高水平的电离辐射靶向肝内肿瘤。该试验旨在通过在局部肝动脉化疗(HAC)方案中添加单次SIR-Spheres治疗,以氟尿苷输注12天并每月间隔的方式进行测量,与单独使用相同的化学疗法相比,可以衡量患者增加的收益。患者与方法:对来自大肠原发性腺癌的双叶不可切除的肝转移患者进行了一项纳入74名患者的III期随机临床试验。该试验中评估的患者获益标准是肿瘤反应,肝脏疾病进展时间,总生存期,生活质量以及与治疗相关的毒性。肿瘤反应通过横截面肿瘤面积和总肿瘤体积的连续变化来衡量,只要持续至少三个月以及血清癌胚-胚胎抗原(CEA)的变化即可。结果:按肿瘤面积(44%vs. 17.6%,P = 0.01)肿瘤体积测量(50%vs. 24%),接受SIR-Spheres的患者的部分和完全缓解率(PR + CR)明显更高。 P = 0.03)和CEA(72%比47%,P = 0.004)。与单独接受HAC的患者相比,通过任一肿瘤面积(9.7对15.9个月,P = 0.001),肿瘤体积(7.6对12.0)进行测量时,接受SIR-Spheres的患者中肝脏疾病进展的中位时间明显更长。个月,P = 0.04)或CEA(5.7个月和6.7个月,P = 0.06)。接受SIR-Spheres的患者的一年,两年,三年和五年生存率分别为72%,39%,17%和3.5%,而单独使用HAC的患者分别为68%,29%,6.5%和0%。 Cox回归分析表明,接受SIR-Spheres治疗且生存期超过15个月的患者的生存率有所提高(P = 0.06)。与仅接受HAC的患者相比,接受SIR-Spheres的患者的3-4级治疗相关毒性没有增加,生活质量也没有损失。结论:与单独的相同HAC方案相比,单次注射SIR-Spheres加HAC的组合在增加肿瘤反应和无进展生存方面更为有效。

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