评估卡培他滨治疗晚期结肠癌的疗效和安全性。将晚期结肠癌患者随机分为三组:对照组(n=50,每日剂量2,500mg/m2),中剂量组(n=50,日剂量2,000mg/m2),低剂量组(n=50,日剂量1,500mg/m2)卡培他滨4个周期(12周)。之后,响应率,生活质量,收集3组不良反应进行比较。有效率为50%,70%,72%,分别,低剂量组疗效最高(χ2=6.424,p=0.040);生活质量比较结果显示身体功能存在显着差异(F=98.528,p<0.001),作用函数(F=123.418,p<0.001),社会功能(F=89.539,p<0.001),情绪功能(6F=77.295,p<0.001),认知功能(F=83.529,p<0.001),三组的总体生活质量(F=99.528,p<0.001),三组得分一致,低剂量组得分最高。发病率为86.00%,46.00%,34.00%,其中对照组的发生率最高(χ2=16.505,p<0.001)。卡培他滨在1,500mg/m2的剂量下显示出良好的治疗效果,并改善了晚期结肠癌患者的生活质量。不良反应发生率较低。建议延长治疗周期并减少剂量以进一步改善治疗结果和患者预后。试验注册该研究于2024年1月30日在clicaltrials.gov\'NCT06246461\'上注册。
To assess the efficacy and safety of capecitabine in treating advanced colon cancer. Patients with advanced colon cancer were randomized into three groups: control group (n = 50, daily dose 2,500 mg/m2), the medium-dose group (n = 50, daily dose 2,000 mg/m2), and the low-dose group (n = 50, daily dose 1,500 mg/m2) capecitabine for 4 cycles(12 weeks). Afterwards, the response rate, quality of life, and adverse reactions of the three groups were collected for comparison. Efficacy rates were 50%, 70%, and 72%, respectively, with the low-dose group showing the highest efficacy (χ2 = 6.424, p = 0.040); Quality of life comparison results indicated significant differences in physical function (F = 98.528, p < 0.001), role function (F = 123.418, p < 0.001), social function(F = 89.539, p < 0.001), emotional function (6 F = 77.295, p < 0.001), cognitive function (F = 83.529, p < 0.001), and overall quality of life (F = 99.528, p < 0.001) among the three groups, and the three groups returned consistent scores, with the low-dose group scoring highest. Incidence rates were 86.00%, 46.00%, 34.00%, with the control group having the highest rate (χ2 = 16.505, p < 0.001). Capecitabine at a dosage of 1,500 mg/m2 demonstrated a good therapeutic effect and improved the quality of life in patients with advanced colon cancer, with a lower incidence of adverse reactions. A prolonged treatment cycle with reduced dosage is suggested to further improve treatment outcomes and patient prognosis. Trial registration The study was registered on clicaltrials.gov \'NCT06246461\' on 30/01/2024.