Kunheri B, Gurram B, Madhavan R, Makuny D
Department of Radiotherapy, Amrita School of Medicine, Amrita Viswavidyapeetham University, Kochi, Kerala, India.
Indian J Cancer. 2016 Oct-Dec;53(4):518-523. doi: 10.4103/0019-509X.204777.
Preoperative concurrent chemoradiation therapy (CRT) with either capecitabine or 5-florouracil/leucovorin (5 FU/LV) is the standard of care in locally advanced rectal cancer (LARC). Literature comparing the toxicity and response of these two regimens in Indian patients is sparse. Our objective was to compare the pathological response (PR) and clinical outcome of capecitabine versus 5 FU/LV in CRT for LARC.
Sixty patients with LARC treated with preoperative CRT with capecitabine or 5FU/LV from January 2009 to May 2014 were analyzed. Ryan's tumor regression grading was used for PR assessment and tumor downstaging was defined as a reduction in the T and N stages by at least one level. Toxicity was assessed with RTOG acute toxicity assessment criteria and CTCAE 4.0 version. Statistical analysis was done using IBM SPSS 20 software. Percentage of patients with respect to response rates and toxicities was computed in each of the treatment groups. To test the statistical significance of the difference in PR rates and toxicities between the two groups, Chi-square test was used. Kaplan-Meier estimate of survival rate was computed for each group. To test the statistical significance of the difference in survival rate, the log-rank test was applied.
The two groups (5 FU/LV vs. capecitabine) were comparable with respect to pathological complete response (20% vs. 24%), pathological downstaging (76% vs. 69%), sphincter preservation rates, and acute complication rates. Both regimens were well tolerated. Overall survival and disease-free survival also did not show a statistically significant difference between the two groups (P values 0.720 and 0.255, respectively). In summary, our analysis showed the equivalence of both regimens in the preoperative CRT setting.
术前使用卡培他滨或氟尿嘧啶/亚叶酸钙(5-FU/LV)进行同步放化疗(CRT)是局部晚期直肠癌(LARC)的标准治疗方法。比较这两种方案在印度患者中的毒性和反应的文献较少。我们的目的是比较卡培他滨与5-FU/LV在LARC同步放化疗中的病理反应(PR)和临床结果。
分析了2009年1月至2014年5月期间接受术前卡培他滨或5-FU/LV同步放化疗的60例LARC患者。采用Ryan肿瘤消退分级进行PR评估,肿瘤降期定义为T和N分期至少降低一级。根据RTOG急性毒性评估标准和CTCAE 4.0版评估毒性。使用IBM SPSS 20软件进行统计分析。计算每个治疗组中患者的反应率和毒性百分比。为检验两组之间PR率和毒性差异的统计学意义,采用卡方检验。计算每组的Kaplan-Meier生存率估计值。为检验生存率差异的统计学意义,应用对数秩检验。
两组(5-FU/LV组与卡培他滨组)在病理完全缓解率(20%对24%)、病理降期率(76%对69%)、括约肌保留率和急性并发症率方面具有可比性。两种方案耐受性均良好。两组的总生存期和无病生存期也未显示出统计学显著差异(P值分别为0.720和0.255)。总之,我们的分析表明在术前同步放化疗环境中两种方案等效。