以白蛋白结合型紫杉醇为基础的方案治疗晚期肺癌的临床疗效及安全性观察
[Abstract]:Background and objective Albumin binding paclitaxel is a new type of paclitaxel preparation which combines human blood albumin with paclitaxel without cosolvent. The purpose of this study was to observe the clinical efficacy and safety of albumin-combined paclitaxel in the treatment of advanced lung cancer. Methods from November 2011 to December 2014, 50 patients with advanced / non-operative advanced lung cancer were selected. Albumin-binding paclitaxel 130 mg/m2, was given on day 1, day 8, single or combined regimen, 21 days as a cycle, and the adverse reactions were observed in each cycle. The imaging efficacy was evaluated according to the solid tumor efficacy evaluation standard (Response Evaluation Criteria in Solid Tumors,RECIST) every 2 cycles. Results the overall objective effective rate of albumin-combined paclitaxel was 20% (overall response rate,ORR) and the disease control rate (disease control rate,DCR) was 68%. In subgroup analysis, ORR and ORR were 26.7% and 80%, respectively, which were significantly better than those of other pathological types, but there was no statistical difference. ORR (36.4%vs 15.4%) could be increased by antiangiogenic therapy on the basis of albumin-bound paclitaxel single drug or combination of two drugs. The DCR of patients treated with four lines or more could still reach 69.2%. The main adverse reactions were hematological toxicity but controllable, no hypersensory reaction and grade 4 adverse reaction. Conclusion Albumin-combined paclitaxel is effective in the treatment of advanced lung cancer regardless of its pathological type and the number of therapeutic lines, and has more advantages in combination with anti-vascular targeting therapy. Even for the elderly and patients after multiline treatment, tolerance is better.
【作者单位】: 北京医院肿瘤内科 国家老年医学中心;
【分类号】:R734.2
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