Royal Marsden NHS Foundation Trust, Department of Medicine, Royal Marsden Hospital, Downs Road, Sutton, Surrey, UK.
J Thorac Oncol. 2010 Sep;5(9):1397-403. doi: 10.1097/JTO.0b013e3181eba7f9.
Previous studies investigating the effect of increased dose intensity and chemotherapy-induced neutropenia in patients with advanced non-small cell lung cancer (NSCLC) have not consistently shown significant survival benefits.
This retrospective analysis reviewed the outcome of patients receiving palliative chemotherapy for advanced NSCLC (stages III-IV) at the Royal Marsden Hospital. Regimens included cisplatin or carboplatin with either vinorelbine or gemcitabine on days 1 and 8, every 21 days. Patients who received at least four cycles of chemotherapy were classified into groups based on dose intensity, dose reductions, and worst grade of neutropenia for a landmark analysis. Comparisons between these groups for time to progression and overall survival were made by standard univariate and multivariate methods.
One hundred sixty-nine of a total of 190 patients who received more than four cycles of chemotherapy during the period between November 1998 and December 2008 were included. One hundred twenty-five (73.9%) patients received four chemotherapy cycles with the remaining receiving up to six cycles. The median relative dose intensity for platinum was 93.9% (62.1-102%) and for vinorelbine/gemcitabine was 91.7% (37.8-105%). Dose reductions were recorded in 64 patients (37.8%), and 65 patients (38.5%) had grades 3 to 4 neutropenia. There were no statistically significant differences in time to progression and overall survival between any of the subgroups.
This retrospective analysis demonstrates no significant relationship between survival and dose intensity (<90%), modest dose reductions (<20%), or chemotherapy-induced neutropenia in patients receiving standard doublet platinum containing chemotherapy in NSCLC.
先前研究调查剂量强度增加和化疗引起的中性粒细胞减少症对晚期非小细胞肺癌(NSCLC)患者的影响,并未一致显示出显著的生存获益。
本回顾性分析回顾了皇家马斯登医院接受姑息性化疗的晚期 NSCLC(III-IV 期)患者的结局。方案包括顺铂或卡铂联合长春瑞滨或吉西他滨,第 1 和 8 天给药,每 21 天 1 次。至少接受 4 个周期化疗的患者根据剂量强度、剂量减少和中性粒细胞减少的最差等级进行分组,用于里程碑分析。通过标准单变量和多变量方法比较这些组的无进展生存期和总生存期。
在 1998 年 11 月至 2008 年 12 月期间,共 190 例接受超过 4 个周期化疗的患者中,共有 169 例患者纳入本研究。125 例(73.9%)患者接受 4 个周期化疗,其余患者接受最多 6 个周期化疗。铂类的中位数相对剂量强度为 93.9%(62.1-102%),长春瑞滨/吉西他滨为 91.7%(37.8-105%)。64 例(37.8%)患者记录了剂量减少,65 例(38.5%)患者发生 3-4 级中性粒细胞减少症。任何亚组之间的无进展生存期和总生存期均无统计学差异。
本回顾性分析表明,在接受标准双联铂类化疗的 NSCLC 患者中,生存与剂量强度(<90%)、适度剂量减少(<20%)或化疗引起的中性粒细胞减少之间无显著关系。