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首页> 外文期刊>In vivo. >Safety and Efficacy of Trifluridine-Tipiracil Hydrochloride Oral Combination (TAS-102) in Patients with Unresectable Colorectal Cancer
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Safety and Efficacy of Trifluridine-Tipiracil Hydrochloride Oral Combination (TAS-102) in Patients with Unresectable Colorectal Cancer

机译:不可手术切除的结直肠癌患者中三氟哌啶-替吡拉酯盐酸盐口服联合使用(TAS-102)的安全性和有效性

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Aim: To retrospectively examine efficacy and safety of oral combination of trifluridine and tipiracil hydrochloride (TAS-102) as the second-line therapeutic agent for unresectable colorectal cancer. Patient and Methods: Treatment outcomes of 17 patients who had received TAS-102 at our Institution from January 2015 to January 2017 were analyzed. The indications for second-line TAS-102 treatment were intolerance to other multi-drug combination (four patients) or patient refusal of the standard second-line therapy (13 patients). Results: Among 17 patients who received TAS-102 as second-line therapy, partial response was observed in two (12%) and stable disease in two (12%). Outcomes of TAS-102 given as second-line therapy were: median overall survival of 5 months, response rate of 12% and disease control of 24%. Overall, no adverse events other than neutropenia were noted. Conclusion: Our findings suggest a beneficial role of TAS-102 in second-line therapy for unresectable colorectal carcinoma.
机译:目的:回顾性研究口服三氟吡啶和盐酸替吡西酯(TAS-102)作为不可切除结直肠癌的二线治疗药物的疗效和安全性。患者和方法:分析了2015年1月至2017年1月在我们机构接受TAS-102治疗的17例患者的治疗结果。 TAS-102二线治疗的适应症是对其他多种药物组合不耐受(四名患者)或拒绝标准二线治疗的患者(13例)。结果:在接受TAS-102作为二线治疗的17例患者中,有2例(12%)观察到局部缓解,有2例(12%)观察到疾病稳定。作为二线治疗的TAS-102结果为:中位总生存期为5个月,缓解率为12%,疾病控制率为24%。总体而言,除中性粒细胞减少以外,未观察到其他不良事件。结论:我们的发现表明TAS-102在不可切除的结直肠癌的二线治疗中具有有益的作用。

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