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作 者:冯燕茹[1] 金晶[1] 王鑫[1] 肖琴[1] 王维虎[1] 王淑莲[1] 刘跃平[1] 宋永文[1] 任骅[1] 房辉[1] 李宁[1] 李晔雄[1] 刘新帆[1] 余子豪[1]
机构地区:[1]北京协和医学院中国医学科学院肿瘤医院放疗科,100021
出 处:《中华放射肿瘤学杂志》2014年第3期199-204,共6页Chinese Journal of Radiation Oncology
基 金:北京希望马拉松专项基金资助(LC2011A11);吴阶平医学基金会临床科研专项资助基金(320.6750.10074)
摘 要:目的 比较Ⅱ、Ⅲ期直肠癌根治术后卡培他滨±奥沙利铂同期放化疗疗效.方法 回顾分析2002-2010年分别接受卡培他滨术后同期放化疗(单药组,427例)和奥沙利铂+卡培他滨术后同期放化疗(双药组,248例)的临床资料.治疗模式均为全直肠系膜切除术+同期放化疗±辅助化疗.放疗方法为真骨盆45.0~50.4 Gy分25次.结果 采用倾向评分配比法按1∶1平衡基线特征后产生单双药组各248例,其中单药、双药组5年样本数分别为81、104例.匹配后单、双药组的5年OS (78.1%∶74.9%)、DFS (74.4%∶67.9%)、LRC (94.5%∶ 92.8%)和DMFS (77.1%∶ 70.9%)均相近(P=0.547、0.292、0.484、0.364),但双药组3、4级不良反应发生率显著高于单药组(38.3%∶24.6%,P=0.001).结论 Ⅱ、Ⅲ期直肠癌根治术后卡培他滨+奥沙利铂同期放化疗疗效未优于卡培他滨单药同期放化疗,而不良反应增加.单药卡培他滨同期放化疗仍为标准方案.Objective To compare the efficacy of concurrent chemoradiotherapy (CCRT) with capecitabine and oxaliplatin versus capecitabine alone in stage Ⅱ/Ⅲ rectal cancer patients after radical operation.Methods A retrospective analysis was performed on the clinical data of 675 patients with stage Ⅱ/Ⅲ rectal cancer who received postoperative concurrent chemoradiotherapy (CCRT) with capecitabine (CAP group,n =427) or capecitabine and oxaliplatin (CAPOX group,n =248) from 2002 to 2010.The treatment modality was total mesorectal excision + CCRT ± adjuvant chemotherapy.Radiotherapy was delivered to the true pelvis at a dose of 45.0-50.4 Gy/25 fractions.Results The propensity score matching method (1 ∶ 1) was applied to balance the baseline characteristics and assign 248 patients to each group.The 5-year sample sizes for CAP group and CAPOX group were 81,104.There were no significant differences between the two groups in 5-year overall survival (78.1% vs.74.9%,P =0.547),disease-free survival (74.4% vs.67.9%,P =0.292),locoregional control (94.5% vs.92.8%,P =0.484),and distant metastasis-free survival (77.1% vs.70.9%,P =0.364).But grade 3/4 toxicities occurred in 24.6% of patients in the CAP group,versus 38.3% in the CAPOX group (P =0.001).Conclusions CCRT with oxaliplatin and capecitabine has no survival advantage over CCRT with capecitabine alone and increases the incidence of toxicities in stage Ⅱ/Ⅲ rectal cancer patients after radical operation.CCRT with capecitabine alone is still the standard regimen.
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