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A clinical trial on docetaxel and carboplatin therapy with or without nimotuzumab for the treatment of advanced nonsmall cell lung cancer

机译:多西他赛联合卡铂联合或不联合尼莫妥单抗治疗晚期非小细胞肺癌的临床试验

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Background: To evaluate the role of nimotuzumab in combination with chemotherapy in patients with advanced nonsmall cell lung cancer (NSCLC) through progress-free survival, changes in tumor marker expression and adverse drug reactions. Materials and Methods: A total of 59 NSCLC patients were randomized into two groups. The treatment group (n = 30) received nimotuzumab (200 mg) with docetaxel (60 mg/m 2 ) and carboplatin (area under curve = 5), whereas the control group (n = 29) received chemotherapy at the same dosage. All patients received two cycles of treatment lasting for 42 days. The serum tumor biomarker levels were measured on the day before treatment and at 60 days after treatment. Results: The efficacy of treatment for the treatment and control groups were 36.7% and 27.6%, respectively; this difference was not statistically significant. However, progression-free survival (PFS) was significantly prolonged by 1 month in the treatment group. Peripheral blood CYFRA21-1 decreased significantly during treatment with a more extensive decrease in the treatment group, although the difference between the groups was not statistically significant. The neuron-specific enolase levels significantly decreased across all 59 patients. The carcinoembryonic antigen levels decreased significantly in the treatment group, but remained stable in the control group throughout the treatment period. Nimotuzumab was well tolerated by patients with only three cases of Grades I and II skin rash and no other toxic symptoms. Conclusion: Nimotuzumab with docetaxel and carboplatin can enhance the short-term clinical efficacy by extending the duration of PFS and was generally well tolerated by patients.
机译:背景:通过无进展生存期,肿瘤标志物表达的变化和药物不良反应,评估尼莫妥单抗联合化疗在晚期非小细胞肺癌(NSCLC)患者中的作用。材料和方法:将59例NSCLC患者随机分为两组。治疗组(n = 30)接受尼莫珠单抗(200 mg),多西他赛(60 mg / m 2 )和卡铂(曲线下面积= 5),而对照组(n = 29)相同剂量的化疗。所有患者均接受两个疗程,持续42天。在治疗前一天和治疗后60天测量血清肿瘤生物标志物水平。结果:治疗组和对照组的治疗效率分别为36.7%和27.6%;这种差异没有统计学意义。但是,治疗组的无进展生存期(PFS)明显延长了1个月。治疗期间外周血CYFRA21-1显着下降,治疗组更广泛地下降,尽管两组之间的差异无统计学意义。在所有59例患者中,神经元特异性烯醇化酶水平均显着下降。在整个治疗期间,治疗组的癌胚抗原水平显着降低,但在对照组中保持稳定。只有三例I级和II级皮疹且无其他中毒症状的患者对Nimotuzumab有很好的耐受性。结论:尼莫妥单抗联合多西他赛和卡铂可以延长PFS的持续时间,从而提高短期临床疗效,患者普遍耐受。

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