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Adjuvant Chemotherapy of Gemcitabine plus Carboplatin versus Paclitaxel plus Carboplatin in Patients with Resected Non-Small Cell Lung Cancer

机译:吉西他滨联合卡铂与紫杉醇联合卡铂对非小细胞肺癌患者的辅助化疗

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Background: This retrospective study was to evaluate the efficacy and toxicity of gemcitabine plus carboplatin (GC regimen) and paclitaxel plus carboplatin (PC regimen) combination chemotherapy administered as an adjuvant therapy after complete resection of non-small cell lung cancer. Methods: Forty-four patients (GC regimen, n = 29; PC regimen, n = 15) received gemcitabine at a dose of 1000 mg/m2 on days 1 and 8, and carboplatin with the target dose of area under the curve (AUC) of 4 on day 8 every 28 days and paclitaxel at a dose of 70 mg/m2 on days 1, 8 and 15, and carboplatin with the target dose of AUC of 5 on day 1 every 28 days. Results: A total of 130 cycles of the treatment were administered (averaged, 3.1 in GC arm and 2.7 cycles in PC arm). Forty-three patients (97.7%) completed the scheduled cycles. One patient (2.3%) was discontinued due to grade 4 pneumonia. The dose was reduced in 2 patients (4.5%) due to grade 4 thrombocytopenia. Grade 3/4 neutropenia was significantly observed in the PC group (GC: 12/29, 41.4%; PC: 11/15, 73.3%, p = 0.0443). The nonhematological toxicities were mild. Grade 1/2 alanine aminotransferase and aspartate aminotransferase in the GC group was significantly observed higher compared to those of the PC group (GC: 20/29, 69.0%; PC: 4/15, 26.7%, p = 0.0076). Grade 1/2 alopecia was significantly observed in the PC group (GC: 0/25, 0.0%; PC: 13/15, 86.7%, p 0.0001). There was no treatment-related death. The median survival time (MST) of the entire GC group was 784 days, the 3-year overall survival (OS) was 75.9%, and 3-year recurrence-free survival (RFS) was 65.5%. The MST of the entire PC group was 963 days, the 3-year OS was 80.0%, and the 3-year RFS was 60.0%. Conclusion: These results demonstrate that the GC and PC combination chemotherapies are efficacious and feasible regimens, which should be considered as one of the standard therapies for adjuvant therapy.
机译:背景:这项回顾性研究旨在评估吉西他滨加卡铂(GC方案)和紫杉醇加卡铂(PC方案)联合化疗作为非小细胞肺癌完全切除后辅助治疗的疗效和毒性。方法:44名患者(GC方案,n = 29; PC方案,n = 15)在第1天和第8天接受吉西他滨的剂量为1000 mg / m2,并接受卡铂治疗,曲线下面积为目标剂量(AUC) ),每28天第8天为4),紫杉醇在第1、8和15天为70 mg / m2剂量,卡铂在第28天的第1天为AUC目标剂量为5。结果:总共进行了130个治疗周期(平均,GC组为3.1周期,PC组为2.7个周期)。四十三名患者(97.7%)完成了预定的周期。一名患者(2.3%)因发生4级肺炎而中断治疗。由于4级血小板减少症,有2例患者的剂量减少了(4.5%)。在PC组中观察到3/4级中性粒细胞减少(GC:12/29,41.4 %; PC:11/15,73.3 %,p = 0.0443)。非血液学毒性轻微。与PC组相比,GC组的1/2级丙氨酸氨基转移酶和天冬氨酸氨基转移酶显着高于PC组(GC:20 / 29,69.0%; PC:4 / 15,26.7%,p = 0.0076)。在PC组中明显观察到1/2级脱发(GC:0/25,0.0 %; PC:13/15,86.7 %,p 0.0001)。没有与治疗有关的死亡。整个GC组的中位生存时间(MST)为784天,3年总生存率(OS)为75.9 %,3年无复发生存率(RFS)为65.5 %。整个PC组的MST为963天,三年OS为80.0%,RFS为60.0%。结论:这些结果表明,GC和PC联合化疗是有效可行的方案,应被视为辅助治疗的标准疗法之一。

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