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Serum neuron-specific enolase (S-NSE) and the prognosis in small-cell lung cancer (SCLC): a combined multivariable analysis on data from nine centres

机译:血清神经元特异性烯醇化酶(S-NSE)和小细胞肺癌(SCLC)的预后:对来自9个中心的数据进行的多变量组合分析

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The influence of pretreatment serum neuron-specific enolase (S-NSE) in addition to more conventional prognostic factors on survival duration in small-cell lung cancer (SCLC) was investigated in 770 patients from nine centres in six countries. The other variables included stage of disease, performance status (PS), age, sex, serum lactate dehydrogenase (S-LDH), serum alkaline phosphatase (S-AP), and serum carcinoembryonic antigen (S-CEA). Increased values of S-NSE (> 12.5 micrograms-1 l) were observed in 81% of the patients, whereas S-LDH, S-AP and S-CEA were elevated in only half of the patients or less. Multivariable analysis by Cox's proportional hazard model disclosed S-NSE as the most powerful prognostic factor followed by poor PS and extensive stage disease. If PS was ignored, S-LDH came up as a significant prognostic factor. S-AP, S-CEA, age and sex had no significant influence on the prognosis. The three prognostic factors, S-NSE, PS and stage of disease, enabled establishment of a prognostic index (PI) based on a simple algorithm PI = zNSE + z(stage) + 2zPS. This segregated the patients into four groups with clearly different prognosis. The median survival and 95% confidence intervals of the four groups were: 468 days (540-408), 362 days (405-328), 256 days (270-241) and 125 days (179-58). Based on the present results we recommend S-NSE and PS, in addition to stage, for prognostic stratification in treatment trials on SCLC.
机译:在六个国家的9个中心的770名患者中,研究了预处理血清神经元特异性烯醇化酶(S-NSE)以及更常规的预后因素对小细胞肺癌(SCLC)生存期的影响。其他变量包括疾病阶段,表现状态(PS),年龄,性别,血清乳酸脱氢酶(S-LDH),血清碱性磷酸酶(S-AP)和血清癌胚抗原(S-CEA)。在81%的患者中观察到S-NSE值升高(> 12.5微克-1 l),而只有一半或更少的患者中S-LDH,S-AP和S-CEA升高。通过Cox比例风险模型进行的多变量分析显示,S-NSE是最有力的预后因素,其次是PS差和广泛分期疾病。如果忽略PS,则S-LDH成为重要的预后因素。 S-AP,S-CEA,年龄和性别对预后无明显影响。 S-NSE,PS和疾病分期这三个预后因素可以基于简单算法PI = zNSE + z(分期)+ 2zPS建立预后指数(PI)。这将患者分为四组,其预后明显不同。四组的中位生存期和95%置信区间为468天(540-408),362天(405-328),256天(270-241)和125天(179-58)。根据目前的结果,除分期外,我们还建议在SCLC的治疗试验中将S-NSE和PS用于预后分层。

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