Pujol J-L, Molinier O, Ebert W, Daurès J-P, Barlesi F, Buccheri G, Paesmans M, Quoix E, Moro-Sibilot D, Szturmowicz M, Bréchot J-M, Muley T, Grenier J
Montpellier Academic Hospital, Hôpital Arnaud de Villeneuve, Avenue du Doyen Giraud, 34295 Montpellier Cedex 5, France.
Br J Cancer. 2004 Jun 1;90(11):2097-105. doi: 10.1038/sj.bjc.6601851.
The purpose of this study was to determine the prognostic significance of a high pretreatment serum CYFRA 21-1 level (a cytokeratin 19 fragment) adjusted for the effects of well-known co-variables in non-small-cell lung cancer (NSCLC). This meta-analysis based on individual updated data gathered comprehensive databases from published or unpublished controlled studies dealing with the prognostic effect of serum CYFRA 21-1 level at presentation in NSCLC of any stage (nine institutions, 2063 patients). Multivariate regression was carried out with the Cox model. The proportional hazard assumption for each of the selected variables retained in the final model was originally checked by log minus log plots baseline hazard ratio. The follow-up ranged from 25 to 78 months. A total of 1616 events were recorded. In the multivariate analysis performed at the 1-year end point, a high pretreatment CYFRA 21-1 level was an unfavourable prognostic determinant in all centres except one (Hazard ratio (95% confidence interval): 1.88 (1.64-2.15), P<10(-4)). Other significant variables were stage of the disease, age and performance status. Within the first 18 months, the procedure disclosed a nearly similar hazard ratio for patients having a high pretreatment serum CYFRA 21-1 level (1.62 (1.42-1.86), P<10(-4)). For patients who did not undergo surgery, the hazard ratio during the first year of follow-up was 1.78 (1.54-2.07), P<10(-4). Finally, in the surgically treated population, at the 2-year end point, a high pretreatment CYFRA 21-1 and a locally advanced stage remained unfavourable prognostic determinants. In conclusion CYFRA 21-1 might be regarded as a putative co-variable in analysing NSCLC outcome inasmuch as a high serum level is a significant determinant of poor prognosis whatever the planned treatment.
本研究的目的是确定在非小细胞肺癌(NSCLC)中,校正了已知协变量影响后的高预处理血清CYFRA 21-1水平(一种细胞角蛋白19片段)的预后意义。这项基于个体更新数据的荟萃分析收集了已发表或未发表的对照研究的综合数据库,这些研究涉及血清CYFRA 21-1水平对任何阶段NSCLC患者预后的影响(九个机构,2063例患者)。使用Cox模型进行多变量回归。最终模型中保留的每个选定变量的比例风险假设最初通过对数减对数图基线风险比进行检查。随访时间为25至78个月。共记录了1616例事件。在1年终点进行的多变量分析中,除一个中心外,所有中心的高预处理CYFRA 21-1水平都是不良预后的决定因素(风险比(95%置信区间):1.88(1.64-2.15),P<10(-4))。其他显著变量为疾病分期、年龄和体能状态。在最初18个月内,该程序显示,预处理血清CYFRA 21-1水平高的患者的风险比几乎相似(1.62(1.42-1.86),P<10(-4))。对于未接受手术的患者,随访第一年的风险比为1.78(1.54-2.07),P<10(-4)。最后,在接受手术治疗的人群中,在2年终点时,高预处理CYFRA 21-1水平和局部晚期仍然是不良预后的决定因素。总之,CYFRA 21-1可被视为分析NSCLC预后的一个假定协变量,因为无论计划采用何种治疗方法,高血清水平都是预后不良的重要决定因素。