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Clinical predictive value of in vitro anticancer drug sensitivity test for the therapeutic effect of adjuvant chemotherapy in patients with stage II–III colorectal cancer

机译:体外抗癌药敏感性试验对Ⅱ〜Ⅲ期大肠癌辅助化疗疗效的临床预测价值

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摘要

Clinically useful predictors of the efficacy of adjuvant chemotherapy following curative colorectal surgery remain to be determined. In the present study, we investigated the clinical utility of the collagen gel droplet-embedded culture drug sensitivity test (CD-DST) as a predictor of the therapeutic response to 5-fluorouracil (5-FU)-based adjuvant chemo-therapy in patients with stage II–III colorectal cancer. CD-DST was conducted using tumor samples surgically obtained from 189 patients. The therapeutic effect of 5-FU-based regimens between high (high-group) and low (low-group) sensitivity groups and a group that did not receive chemotherapy [CTx(-) group] was compared. CD-DST was successfully performed in 151 out of the 189 patients (79.9%), 87 of whom received 5-FU-based adjuvant chemotherapy after surgery. Twenty-seven of these 87 patients (31.0%) were classified as the high-group and the remaining 60 (69.0%) as the low-group. The 5-year recurrence-free survival (RFS) in the high-group was significantly higher compared to that in the low- and the CTx(-) groups. No differences in the 5-year RFS were observed between the low- and CTx(-) groups. In conclusion, CD-DST appears to be useful for predicting the therapeutic response to 5-FU-based adjuvant chemotherapy in patients with stage II-III colorectal cancer.
机译:大肠癌根治术后辅助化疗疗效的临床有用预测指标仍有待确定。在本研究中,我们调查了胶原凝胶微滴包埋的培养药物敏感性试验(CD-DST)作为患者对基于5氟尿嘧啶(5-FU)的辅助化学疗法的治疗反应的预测指标的临床实用性II-III期大肠癌。使用从189例患者手术获得的肿瘤样本进行CD-DST。比较了在高(高组)和低(低组)敏感性组与未接受化疗的组[CTx(-)组]之间基于5-FU方案的治疗效果。 189例患者中有151例成功进行了CD-DST(79.9%),其中87例术后接受了基于5FU的辅助化疗。在这87位患者中,有27位(31.0%)被归为高组,其余60位(69.0%)被归为低组。高组的5年无复发生存率(RFS)显着高于低组和CTx(-)组。低组和CTx(-)组之间的5年RFS没有差异。总之,CD-DST似乎可用于预测II-III期大肠癌患者对基于5-FU的辅助化疗的治疗反应。

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