Department of Medicine, All India Institute of Medical Sciences (AIIMS), Ansari Nagar, New Delhi 110 029, India.
Cytokine. 2010 Sep;51(3):245-8. doi: 10.1016/j.cyto.2010.05.007.
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.
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.
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.
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.
越来越多的证据表明细胞毒性治疗后细胞因子谱发生变化。我们假设,在肺癌化疗过程中血浆肿瘤坏死因子-α(TNF-α)水平的变化可能可以早期预测治疗效果。
42 例晚期非小细胞肺癌患者在化疗前第 1、2 和 3 个周期时检测血浆 TNF-α水平,并在第 3 个化疗周期后通过计算机断层扫描评估治疗反应与该水平进行相关性分析。
在各个治疗周期前测量的 TNF-α水平不能区分缓解、无变化和进展的患者。为了预测治疗反应不足,在 100%特异性下,使用第 1 和第 2 个治疗周期前测量的 TNF-α水平,其灵敏度分别为 11.5%和 23.1%。在第 2 个治疗周期前测量的 TNF-α水平,其灵敏度为 14.3%,特异性为 100%,可以预测疾病进展。在各个治疗周期前测量的 TNF-α水平与生存无关。
TNF-α的测量可能无法证明是预测 NSCLC 早期治疗效果的良好生物标志物。需要额外的、更特异和更敏感的基于血液的生物标志物,以进一步提高当前用于指示早期治疗效果的成像工具的诊断能力。