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首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Early Experience with 70-150 mu m Irinotecan Drug-eluting Beads (M1-DEBIRI) for the Treatment of Unresectable Hepatic Colorectal Metastases
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Early Experience with 70-150 mu m Irinotecan Drug-eluting Beads (M1-DEBIRI) for the Treatment of Unresectable Hepatic Colorectal Metastases

机译:70-150微米伊立替康药物洗脱珠(M1-DEBIRI)治疗不可切除的肝结直肠转移瘤的早期经验

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摘要

Aim: To report our early experience on the feasibility and safety of 70-150 mu m drug-eluting beads loaded with irinotecan (M1-DEBIRI) for treating unresectable hepatic colorectal metastases. Patients and Methods: An Institutional Review Board-approved, prospectively maintained, multi-institutional registry was evaluated from 2/2009 to 8/2013. Fifteen consecutive patients presenting with liver-dominant metastatic colorectal cancer were treated with M1-DEBIRI. Kaplan-Meier statistics was used to evaluate hepatic progression-free-survival and overall survival. Results: Fifteen patients underwent 32 DEBIRI treatments. The mean prescribed dose was 100 mg of irinotecan (range=100-200 mg). In 75% of treatments (n= 24), 100% of the prescribed dose was delivered before complete stasis. In 97% of treatments (n= 31), at least 50% (median 100 mg, range 25-150 mg) of the prescribed dose was delivered. There was grade 2 abdominal pain after one treatment (3%). In another patient, increased total bilirubin (1.1 to 3.1 mg/dl) was seen after one treatment. There was 42% reduction in median carcinoembryonic antigen level and 33% (5/15 patients) with Response Evaluation Criteria in Solid Tumors (RECIST) objective response (complete and partial). Modified RECIST and European Association for the study of the Liver (EASL) objective response rates were both 73% (11/15 patients). The disease control rate was 93% (14/15 patients). Hepatic progression-free-survival and overall survival were 8 and 13 months respectively. Disease in one patient was down-staged to resection (6%). Conclusion: M1-DEBIRI appears to be safe and feasible in the treatment of metastatic colorectal cancer. Smaller beads also provide efficient irinotecan dose delivery. Larger studies are needed to validate these findings.
机译:目的:报告我们关于负载伊立替康(M1-DEBIRI)的70-150μm药物洗脱微珠治疗不可切除的肝结直肠转移瘤的可行性和安全性的早期经验。患者和方法:从2/2009到8/2013对机构审查委员会批准,前瞻性维护的多机构注册表进行了评估。 M1-DEBIRI治疗连续15例以肝脏为主的转移性结直肠癌患者。 Kaplan-Meier统计量用于评估肝无进展生存期和总生存期。结果:15例患者接受了32次DEBIRI治疗。平均处方剂量为100毫克伊立替康(范围= 100-200毫克)。在75%的治疗中(n = 24),完全停滞前已交付100%的处方剂量。在97%的治疗中(n = 31),至少提供了规定剂量的50%(中位数100 mg,范围25-150 mg)。一次治疗后出现2级腹痛(3%)。在另一位患者中,一次治疗后发现总胆红素增加(1.1至3.1 mg / dl)。实体瘤反应评估标准(RECIST)客观反应(完全和部分)的中位癌胚抗原水平降低了42%,而中位癌胚抗原水平降低了33%(5/15例)。改良的RECIST和欧洲肝病研究协会(EASL)的客观缓解率均为73%(11/15例)。疾病控制率为93%(14/15例)。肝无进展生存期和总生存期分别为8个月和13个月。一名患者的疾病被降级为切除术(6%)。结论:M1-DEBIRI治疗转移性结直肠癌似乎是安全可行的。较小的珠粒也提供有效的伊立替康剂量递送。需要更大的研究来验证这些发现。

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