Frasci G, Lorusso V, Panza N, Comella P, Nicolella G, Bianco A, De Cataldis G, Iannelli A, Bilancia D, Belli M, Massidda B, Piantedosi F, Comella G, De Lena M
Division of Medical Oncology, City Hospital, Avellino, Italy.
J Clin Oncol. 2000 Jul;18(13):2529-36. doi: 10.1200/JCO.2000.18.13.2529.
To evaluate whether the addition of gemcitabine (G) to vinorelbine (V) improves survival and quality of life (QoL) among elderly patients with advanced non-small-cell lung cancer (NSCLC).
Patients with NSCLC aged >/= 70 years with advanced disease were randomly allocated to receive V 30 mg/m(2) on days 1 and 8 every 3 weeks or G 1,200 mg/m(2) + V 30 mg/m(2) on days 1 and 8 every 3 weeks. The estimated sample size was 120 patients per arm, but an interim analysis of survival was planned based on the first 60 patients per arm.
In May 1999, the survival data were analyzed of 120 eligible patients (V group = 60; G + V group = 60) who had been randomized from June 1997 to February 1999. Forty-nine patients had stage IIIB disease, and 71 had stage IV. At a median potential follow-up of 14 months (range, 3 to 22 months), 93 patients had died (G + V group = 41; V group = 52). In the G + V group, median survival time was 29 weeks and projected 1-year survival was 30%; these values were 18 weeks and 13% in the V group. According to multivariate Cox analysis, the risk of death in the G + V arm compared with the V arm was 0.48 (95% confidence interval, 0. 29 to 0.79; P <.01). Combination therapy was also associated with a clear delay in symptom and QoL deterioration. The overall response rates were 22% and 15% in the G + V and V groups, respectively.
In elderly patients with NSCLC, G + V treatment is associated with significantly better survival than is V alone.
评估吉西他滨(G)联合长春瑞滨(V)是否能提高老年晚期非小细胞肺癌(NSCLC)患者的生存率和生活质量(QoL)。
年龄≥70岁的晚期NSCLC患者被随机分配,每3周的第1天和第8天接受V 30 mg/m²,或每3周的第1天和第8天接受G 1200 mg/m² + V 30 mg/m²。预计每组样本量为120例患者,但计划根据每组前60例患者进行生存期中分析。
1999年5月,分析了1997年6月至1999年2月随机分组的120例符合条件的患者(V组 = 60例;G + V组 = 60例)的生存数据。49例患者为ⅢB期疾病,71例为Ⅳ期。中位潜在随访时间为14个月(范围3至22个月),93例患者死亡(G + V组 = 41例;V组 = 52例)。在G + V组中,中位生存时间为29周,预计1年生存率为30%;V组分别为18周和13%。根据多变量Cox分析,与V组相比,G + V组的死亡风险为0.48(95%置信区间,0.29至0.79;P <.01)。联合治疗还与症状和QoL恶化的明显延迟相关。G + V组和V组的总缓解率分别为22%和15%。
在老年NSCLC患者中,G + V治疗的生存率明显优于单独使用V治疗。