Stasi R, Zinzani L, Galieni P, Lauta V M, Damasio E, Dispensa E, Dammacco F, Venditti A, Del Poeta G, Cantonetti M
Department of Hematology, University of Rome Tor Vergata, Italy.
Eur J Haematol. 1995 Jan;54(1):9-17. doi: 10.1111/j.1600-0609.1995.tb01619.x.
Serum levels of 13 different cytokines and receptors were measured serially in 78 patients with aggressive non-Hodgkin's lymphoma (NHL) treated by 4 cycles of an intensive multi-agent chemotherapy regimen. Recombinant human granulocyte-macrophage colony-stimulating factor (GM-CSF) was administered subcutaneously in 36 of these patients from day + 5 to day + 18 after each chemotherapy. Statistically significantly higher pretreatment levels of interleukin-2 (IL-2), interleukin-6 (IL-6), interleukin-8 (IL-8), interleukin-10 (IL-10), the soluble IL-2 receptor (sIL-2r), the soluble transferrin receptor (sTf-r), and neopterin, were observed in NHL patients as compared to controls (p < 0.001 for all molecules). sIL-2r and sTf-r levels correlated with tumor burden (p < 0.001 and p = 0.003, respectively) whereas IL-6 was higher in patients presenting B symptoms (p < 0.001). Cytokine levels progressively declined to normal ranges in responding patients, while they remained elevated in non-responders. Relapsed patients also presented increased concentrations of several molecules. During the administration of GM-CSF, we observed the drastic increase of sIL-2r, while lower elevations were recorded for a number of cytokines, including IL-8, tumor necrosis factor-alpha, interleukin-1 beta, IL-6, and IL-2. However, upon completion of the induction treatment, cytokine/receptor levels were comparable among individuals with the same type of response, whether or not they had received GM-CSF. No single parameter was found to be of prognostic significance, but the combination of elevated IL-10 and of sIL-2r greater than 3000 U/ml selected a subgroup of 7 patients who failed induction treatment (p = 0.002). These results demonstrate that cytokine and soluble receptor measurements can provide valuable informations for a better management of NHL, in terms both of markers to monitor disease activity and of prognostic indicators.
对78例侵袭性非霍奇金淋巴瘤(NHL)患者采用强化多药化疗方案进行4个周期治疗,并连续检测其血清中13种不同细胞因子和受体的水平。其中36例患者在每次化疗后的第5天至第18天皮下注射重组人粒细胞-巨噬细胞集落刺激因子(GM-CSF)。与对照组相比,NHL患者的白细胞介素-2(IL-2)、白细胞介素-6(IL-6)、白细胞介素-8(IL-8)、白细胞介素-10(IL-10)、可溶性IL-2受体(sIL-2r)、可溶性转铁蛋白受体(sTf-r)和新蝶呤的预处理水平在统计学上显著更高(所有分子p < 0.001)。sIL-2r和sTf-r水平与肿瘤负荷相关(分别为p < 0.001和p = 0.003),而有B症状的患者IL-6水平更高(p < 0.001)。有反应的患者细胞因子水平逐渐降至正常范围,而无反应者则持续升高。复发患者的几种分子浓度也有所增加。在GM-CSF给药期间,我们观察到sIL-2r急剧增加,而包括IL-8、肿瘤坏死因子-α、白细胞介素-1β、IL-6和IL-2在内的多种细胞因子升高幅度较小。然而,诱导治疗完成后,无论是否接受GM-CSF,相同反应类型的个体之间细胞因子/受体水平相当。未发现单一参数具有预后意义,但IL-10升高且sIL-2r大于3000 U/ml的组合筛选出了7例诱导治疗失败的患者亚组(p = 0.002)。这些结果表明,细胞因子和可溶性受体检测可为NHL的更好管理提供有价值的信息,无论是在监测疾病活动的标志物方面还是在预后指标方面。