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小细胞肺癌治疗前及治疗期间神经元特异性烯醇化酶水平的意义

Significance of neuron-specific enolase levels before and during therapy for small cell lung cancer.

作者信息

Bonner J A, Sloan J A, Rowland K M, Klee G G, Kugler J W, Mailliard J A, Wiesenfeld M, Krook J E, Maksymiuk A W, Shaw E G, Marks R S, Perez E A

机构信息

Mayo Clinic, Rochester, Minnesota 55905, USA.

出版信息

Clin Cancer Res. 2000 Feb;6(2):597-601.

Abstract

The level of serum neuron-specific enolase (NSE) has been implicated as a prognostic factor for patients with small cell lung cancer (SCLC). A prospective evaluation was undertaken to assess the prognostic significance of pretreatment NSE and treatment-induced minimum NSE values in patients with SCLC. Patients from two Phase III North Central Cancer Treatment Group trials [one for patients with extensive stage SCLC and one for patients with limited stage SCLC] were asked to enter this laboratory correlational trial. Both trials included treatment with four to six cycles of etoposide and cisplatin, and 121 patients (71 extensive stage SCLC and 50 limited stage SCLC) were entered into the present study of NSE. Pretreatment NSE values and treatment-induced minimum NSE values were independent predictors of time to progression and survival in multivariate analysis. Hazard rate modeling allowed the formulation of specific relationships of NSE to time to progression and survival. Pretreatment NSE levels inversely correlated with time to progression and survival in these patients with SCLC. Pretreatment NSE accounted for 28% of the variance in survival. Both pretreatment NSE and treatment-induced minimum NSE were independent prognostic predictors of time to progression and survival.

摘要

血清神经元特异性烯醇化酶(NSE)水平被认为是小细胞肺癌(SCLC)患者的一个预后因素。开展了一项前瞻性评估,以评估SCLC患者治疗前NSE水平及治疗诱导的最低NSE值的预后意义。来自北中部癌症治疗组两项III期试验(一项针对广泛期SCLC患者,一项针对局限期SCLC患者)的患者被要求参加这项实验室相关性试验。两项试验均包括用依托泊苷和顺铂进行四至六个周期的治疗,121例患者(71例广泛期SCLC患者和50例局限期SCLC患者)进入了目前这项关于NSE的研究。在多变量分析中,治疗前NSE值及治疗诱导的最低NSE值是疾病进展时间和生存时间的独立预测因素。风险率建模使得能够确定NSE与疾病进展时间和生存时间之间的具体关系。在这些SCLC患者中,治疗前NSE水平与疾病进展时间和生存时间呈负相关。治疗前NSE占生存差异的28%。治疗前NSE水平及治疗诱导的最低NSE值均是疾病进展时间和生存时间的独立预后预测因素。

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