Vuoristo M S, Kellokumpu-Lehtinen P, Laine S, Soppi E
Department of Oncology, Tampere University Hospital, Finland.
Immunopharmacol Immunotoxicol. 1996 Aug;18(3):337-54. doi: 10.3109/08923979609052740.
In the present study we evaluated the haematological and immunological changes in 4 patients with advanced melanoma and 6 patients with advanced renal cell carcinoma treated with subcutaneous interleukin (IL)-2 and interferon (IFN)-alfa-2b. Serum samples taken before and during six weeks' courses of IL-2 plus IFN-alfa were assayed for the presence of IL-2, soluble IL-2-receptor (sIL-2R), soluble intercellular adhesion molecule-1 (sICAM-1), IL-6 and IL-8. In addition, whole blood counts were taken. Eosinophilia occurred in all patients, lymphocytosis in 8 patients. The higher maximum level of IL-2 during treatment seemed to be connected to longer survival: it was a median of 578 pg/ml in the patients with a median survival of 7 months, and 1025 pg/ml in the patients who survived a median of 15 months. Conversely, an increase in sIL-2R was an unfavourable sign: it was a median of 8-fold and 3-fold in the patients with a median survival of 7 and 16 months, respectively. During treatment, sICAM-1 levels paralleled with those of sIL-2R. There was major intraindividual and interindividual variation in serum IL-6 and IL-8 levels with no distinctive kinetic pattern. Thus, no definite conclusions could be drawn. However, it seems worthwhile to measure IL-2, sIL-2R and sICAM-1 during immunotherapy; their prognostic value should be further evaluated in a larger patient population.
在本研究中,我们评估了4例晚期黑色素瘤患者和6例晚期肾细胞癌患者接受皮下注射白细胞介素(IL)-2和干扰素(IFN)-α-2b治疗后的血液学和免疫学变化。在IL-2加IFN-α为期六周的疗程之前和期间采集血清样本,检测其中IL-2、可溶性IL-2受体(sIL-2R)、可溶性细胞间黏附分子-1(sICAM-1)、IL-6和IL-8的含量。此外,还进行了全血细胞计数。所有患者均出现嗜酸性粒细胞增多,8例患者出现淋巴细胞增多。治疗期间IL-2的最高水平较高似乎与更长的生存期相关:中位生存期为7个月的患者,IL-2的中位水平为578 pg/ml;中位生存期为15个月的患者,IL-2的中位水平为1025 pg/ml。相反,sIL-2R升高是一个不良迹象:中位生存期为7个月和16个月的患者,sIL-2R分别升高了8倍和3倍。治疗期间,sICAM-1水平与sIL-2R水平平行。血清IL-6和IL-8水平存在较大的个体内和个体间差异,无明显的动力学模式。因此,无法得出明确结论。然而,在免疫治疗期间检测IL-2、sIL-2R和sICAM-1似乎是值得的;它们的预后价值应在更大的患者群体中进一步评估。