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作 者:杨冬阳[1] 黎莹[1] 刘建化[1] 江韦韦[1] 马冬[1]
机构地区:[1]广东省人民医院肿瘤中心肿瘤内科,广东广州510080
出 处:《南方医科大学学报》2013年第12期1815-1818,1830,共5页Journal of Southern Medical University
基 金:广东省科技计划项目(2011B031800285)
摘 要:目的:评价晚期结直肠癌患者联合化疗后卡培他滨维持治疗的临床疗效、安全性、可行性。方法采用回顾性研究方法,分析我科2009年5月~2012年12月住院治疗的73例晚期结直肠癌连续病例,均采用含氟尿嘧啶类联合奥沙利铂或伊立替康化疗。肿瘤达到化疗最大缩小率后,其中42例给予单药卡培他滨1000 mg/m2 bid*14 d/3周的维持治疗至不能耐受或进展;另31例停止化疗随访观察。使用Kaplan-Meier分析两组的疗效,χ2检验分析安全性。结果卡培他滨维持治疗的42例中位PFS为11.6月(95%CI:10.22~11.78),联合化疗的有效率(RR):42.8%。31例停止化疗病例对照观察中位PFS为7.4月(95%CI:5.79~8.21),联合化疗的RR:38.7%。两组RR相似但PFS疗效有统计学差异(P0.05)。结论通过卡培他滨维持治疗的晚期结直肠癌患者得到较长的PFS,且耐受性好,保留了再次进展后接受强烈化疗的可能性,为提高晚期结直肠癌患者生存获益和生活质量提供基础,同时提供了一种有效并有良好耐受性的治疗模式,具有进一步研究探索的可行性和临床前景。Objective To evaluate efficacy, safety, and feasibility of maintenance therapy with capecitabine after fluoropyrimidines/oxaliplatin or fluoropyrimidines/irinotecan chemotherapy in patients with incurable colorectal cancer. Methods Seventy-three hospitalized patients with incurable colorectal cancer who received fluoropyrimidines/oxaliplatin or fluoropyrimidines/irinotecan as the first-line chemotherapy between May 2009 and December 2012 in our department were retrospectively analyzed. When the maximum percentage tumor size reduction was achieved, 42 patients received a maintenance therapy with capecitabine at 1000 mg/m2 in two daily doses on days 1-14, and the other 31 patients without further chemotherapy or the maintenance therapy were followed up. The treatment was repeated every 3 weeks as a cycle until disease progression or intolerable toxicity. The efficacy and safety were evaluated by Kaplan-Meier analysis and χ2 analysis. Results The 42 patients receiving capecitabine maintenance therapy achieved a median progression free survival (PFS) of 11.6 months (95%CI 7.8-15.4), significantly longer than the PFS of 7.4 months (95% CI 4.9-11.8) in the 31 patients without the maintenance therapy (P0.05) except for hand-foot syndrome. Conclusion In patients with incurable colorectal cancer, capecitabine maintenance therapy following combined chemotherapy can achieve a prolonged PFS with a good safety and tolerance and retains the possibility of further intense therapy in the event of disease progression.
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