Zhao Yizhuo, Chen Yurong, Ji Hao, Chu Tianqing, Han Baohui, Liao Meilin
Department of Respiratory Disease, Shanghai Chest Hospital, Shanghai 200030, P.R.China.
Zhongguo Fei Ai Za Zhi. 2004 Oct 20;7(5):449-51. doi: 10.3779/j.issn.1009-3419.2004.05.18.
To compare the effect and toxicity between gemcitabine and cisplatin (GP) with vinorelbine, ifosfamide and cisplatin (NIP) combined chemotherapy in the treatment of patients with advanced non-small cell lung cancer (NSCLC).
Eighty patients received either gemcitabine 1 000 mg/m² on days 1, 8, or 15 plus cisplatin 70-80 mg/m² on day 1, or vinorelbine 25 mg/m² on days 1, 8, ifosfamide 1.2 g/m² on days 1-4 plus cisplatin 70-80 mg/m² on day 1, every 28 days as a cycle.
The objective response rate was 40.0% in GP goup, compared with 52.5% in NIP group (P > 0.05). Median survival time of GP and NIP groups was 13.68 and 15.34 months respectively, and 1-year survival rates were 54.29% and 59.46% respectively (P > 0.05). Leukopenia at grade III+IV was significantly lower in GP arm (27.5%) than that in NIP arm (55.0%) (P < 0.05). Non-hematological toxicities were less frequent in GP group than those in NIP group (P < 0.05).
Although the response rate tends to be higher in three-drug than in two-drug combined chemotherapy, but no significant difference is observed. Three-drug combinations often result in more toxicities. Two-drug combination GP may be the standard protocol for chemotherapy of advanced NSCLC. Three-drug combination NIP should be given to young patients with good performance status.
比较吉西他滨联合顺铂(GP)与长春瑞滨、异环磷酰胺联合顺铂(NIP)在晚期非小细胞肺癌(NSCLC)患者治疗中的疗效及毒性。
80例患者接受以下治疗方案,每28天为一个周期。一组接受第1、8、15天吉西他滨1000mg/m²加第1天顺铂70 - 80mg/m²;另一组接受第1、8天长春瑞滨25mg/m²,第1 - 4天异环磷酰胺1.2g/m²加第1天顺铂70 - 80mg/m²。
GP组客观缓解率为40.0%,NIP组为52.5%(P>0.05)。GP组和NIP组的中位生存时间分别为13.68个月和15.34个月,1年生存率分别为54.29%和59.46%(P>0.05)。GP组III + IV级白细胞减少发生率(27.5%)显著低于NIP组(55.0%)(P<0.05)。GP组非血液学毒性发生率低于NIP组(P<0.05)。
虽然三药联合化疗的缓解率有高于两药联合化疗的趋势,但差异无统计学意义。三药联合化疗通常毒性更大。两药联合GP方案可能是晚期NSCLC化疗的标准方案。三药联合NIP方案应给予身体状况良好的年轻患者。