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首页> 外文期刊>Cancer Cell International >Prospective clinical study of capecitabine plus oxaliplatin concurrent chemoradiotherapy after radical resection of rectal cancer
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Prospective clinical study of capecitabine plus oxaliplatin concurrent chemoradiotherapy after radical resection of rectal cancer

机译:直肠癌根治术后卡培他滨联合奥沙利铂同时放化疗的前瞻性临床研究

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To investigate the efficacy and safety of concurrent chemoradiotherapy with capecitabine or oxaliplatin in locally advanced (T3-4/N?+?M0) rectal cancer. 56 patients with rectal cancer after radical operation were randomly divided into CAPE-OX-CRT group: capecitabine?+?oxaliplatin concurrent chemoradiotherapy (30 cases), CAPE-CRT group: capecitabine concurrent chemoradiotherapy (control, 26 cases). The incidence of grade 1–2 acute toxicity in CAPE-OX-CRT group during concurrent CRT was significantly higher than that in control group, the difference was statistically significant (P 0.05). No grade 4 toxicity was found in both groups. The incidences of interrupted or suspend concurrent chemotherapy in both groups were 19.23% and 46.67%, respectively, P 0.05). The completion rate of adjuvant chemotherapy in control group was higher than that in CAPE-OX-CRT group, but the difference was not statistically significant (P?>?0.05). In postoperative adjuvant chemotherapy, the incidence of bone marrow suppression in CAPE-OX-CRT group was higher than that in control group (P?
机译:探讨卡培他滨或奥沙利铂同时放化疗在局部晚期(T3-4 /Nα+ΔM0)直肠癌中的疗效和安全性。 56例行根治术后直肠癌患者随机分为CAPE-OX-CRT组:卡培他滨+奥沙利铂同时放化疗(30例),CAPE-CRT组:卡培他滨同时放化疗(对照,26例)。同时进行CRT期间CAPE-OX-CRT组1-2级急性毒性的发生率显着高于对照组,差异具有统计学意义(P 0.05)。两组均未发现4级毒性。两组中止或暂停同时化疗的发生率分别为19.23%和46.67%,P <0.05)。对照组的辅助化疗完成率高于CAPE-OX-CRT组,但差异无统计学意义(P≥0.05)。术后辅助化疗中,CAPE-OX-CRT组骨髓抑制的发生率高于对照组(P 0.05),两组的非血液学不良反应发生率相似。卡培他滨联合奥沙利铂并行CRT和奥沙利铂并行CRT对直肠癌根治性切除术后局部晚期直肠癌患者的治疗效果良好。

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