[The clinical analysis of paclitaxel at two dose levels plus carboplatin as the first-line treatment in advanced non-small cell lung cancer]

[紫杉醇两种剂量水平联合卡铂一线治疗晚期非小细胞肺癌的临床分析]

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Abstract

BACKGROUND AND OBJECTIVE: The combination of pacilitaxel and carboplatin has become a widely used regimen in first-line therapy of advanced NSCLC. The aim of this study is to compare the efficacy and safety of paclitaxel plus carboplatin at two dose levels in the first-line treatment of advanced NSCLC patients. METHODS: From Dec 2006 to Jun 2008, 63 patients (ECOG 0-1) with advanced NSCLC were administered with paclitaxel 175 mg/m² (42 patients) plus carboplatin (AUC 5) or paclitaxel 200 mg/m² (21 patients) plus carboplatin (AUC 5), 3-4 weeks/cycle. RESULTS: The objective response rate of paclitaxel 175 mg/m² group and paclitaxel 200 mg/m² group was 28.57% vs 33.33% (P=0.698); median time to progression were 6.7 months vs 7.0 months (P=0.561); median overall survival time were 18.7 months vs 19.0 months (P=0.255); one and two-year survival rate were 61.9% vs 66.7% (P=0.711) and 31.0% vs 33.3% (P=0.852), respectively. Neutropenia 3/4 grade was 61.9% vs 33.3% in paclitaxel 200 mg/m² group and paclitaxel 175 mg/m² group (P=0.031). CONCLUSIONS: 175 mg/m² dose paclitaxel causes less neutropenia than higher dose paclitaxel. Response rate, survival rate, time to progression and survival time are not statistically significant in two groups.

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