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Lack of utility of plasma TNF-alpha level in predicting therapeutic efficacy in patients with advanced non-small cell lung cancer.

机译:血浆TNF-α水平在预测晚期非小细胞肺癌患者的治疗功效方面缺乏实用性。

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BACKGROUND: Accumulating evidence suggests a change in cytokine profile after cytotoxic therapies. We hypothesized that change in plasma levels of tumor necrosis factor-alpha (TNF-alpha) during the course of chemotherapy in lung cancer may predict therapeutic efficacy at an early stage. METHODS: Plasma TNF-alpha levels were quantified before first, second, and third cycle of chemotherapy in 42 patients with advanced non-small cell lung cancer and correlated with response to therapy as assessed by computed tomography after the third chemotherapy cycle. RESULTS: Plasma levels of TNF-alpha measured before various treatment cycles could not differentiate among patients with remission, no change, and progression. For predicting inadequate therapeutic response, a sensitivity of 11.5% and 23.1% was achieved at 100% specificity using plasma TNF-alpha levels measured before first and second therapy cycle, respectively. Prediction of disease progression was achieved with a sensitivity of 14.3% at 100% specificity for plasma TNF-alpha levels measured before second therapy cycle. Plasma levels of TNF-alpha measured before various treatment cycles was not correlated with survival. CONCLUSIONS: Measurement of plasma TNF-alpha may not prove to be a good biomarker for predicting therapeutic efficacy at an early stage in NSCLC. Additional, more specific, and more sensitive blood-based biomarkers will be required to further improve the diagnostic power of current imaging tools for indicating early therapeutic efficacy.
机译:背景:越来越多的证据表明,在进行细胞毒性治疗后,细胞因子谱发生了变化。我们假设在肺癌化疗过程中血浆肿瘤坏死因子-α(TNF-alpha)的水平变化可以预测早期的治疗效果。方法:在42例晚期非小细胞肺癌患者的化疗的第一,第二和第三周期之前,对血浆TNF-α水平进行定量,并与在第三化疗周期后通过计算机断层扫描评估的对治疗的反应相关。结果:在不同治疗周期之前测定的血浆TNF-α水平在缓解,无变化和进展的患者之间无法区分。为了预测不充分的治疗反应,使用分别在第一个和第二个治疗周期之前测得的血浆TNF-α水平,在100%特异性下可获得11.5%和23.1%的敏感性。对疾病进展的预测是通过对第二个治疗周期前测得的血浆TNF-α水平的100%特异性达到14.3%的敏感性实现的。在各种治疗周期之前测得的血浆TNF-α水平与生存率无关。结论:血浆TNF-α的测量可能不能被证明是预测NSCLC早期疗效的良好生物标志物。将需要更多,更具体,更敏感的基于血液的生物标记物,以进一步提高当前成像工具的诊断能力,以指示早期治疗效果。

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