Biggar Robert J, Johansen Julia S, Smedby Karin Ekström, Rostgaard Klaus, Chang Ellen T, Adami Hans-Olov, Glimelius Bengt, Molin Daniel, Hamilton-Dutoit Stephen, Melbye Mads, Hjalgrim Henrik
Department of Epidemiology Research, State Serum Institute, Copenhagen, Denmark.
Clin Cancer Res. 2008 Nov 1;14(21):6974-8. doi: 10.1158/1078-0432.CCR-08-1026.
Serum levels of the inflammatory markers YKL-40 and interleukin 6 (IL-6) are increased in many conditions, including cancers. We examined serum YKL-40 and IL-6 levels in patients with Hodgkin lymphoma, a tumor with strong immunologic reaction to relatively few tumor cells, especially in nodular sclerosis Hodgkin lymphoma.
We analyzed Danish and Swedish patients with incident Hodgkin lymphoma (N=470) and population controls from Denmark (n=245 for YKL-40; n=348 for IL-6). Serum YKL-40 and IL-6 levels were determined by ELISA, and log-transformed data were analyzed by linear regression, adjusting for age and sex.
Serum levels of YKL-40 and IL-6 increased in Hodgkin lymphoma patients compared with controls (YKL-40, 3.6-fold; IL-6, 8.3-fold; both, P<0.0001). In pretreatment samples from pretreatment Hodgkin lymphoma patients (n=176), levels were correlated with more advanced stages (P(trend), 0.0001 for YKL-40 and 0.013 for IL-6) and in those with B symptoms; however, levels were similar in nodular sclerosis and mixed cellularity subtypes, by EBV status, and in younger (<45 years old) and older patients. Patients tested soon after treatment onset had significantly lower levels than pretreatment patients; however, even >or=6 months after treatment onset, serum YKL-40 and IL-6 levels remained significantly increased compared with controls. In patients who died (n=12), pretreatment levels for YKL-40 and IL-6 were higher than in survivors, although not statistically significantly.
Serum YKL-40 and IL-6 levels were increased in untreated Hodgkin lymphoma patients and those with more advanced stages but did not differ significantly by Hodgkin lymphoma histology. Following treatment, serum levels were significantly lower.
炎症标志物YKL-40和白细胞介素6(IL-6)的血清水平在包括癌症在内的多种病症中都会升高。我们检测了霍奇金淋巴瘤患者的血清YKL-40和IL-6水平,霍奇金淋巴瘤是一种对相对较少肿瘤细胞有强烈免疫反应的肿瘤,尤其是在结节硬化型霍奇金淋巴瘤中。
我们分析了丹麦和瑞典的初发霍奇金淋巴瘤患者(N = 470)以及来自丹麦的人群对照(YKL-40检测n = 245;IL-6检测n = 348)。通过酶联免疫吸附测定法(ELISA)测定血清YKL-40和IL-6水平,并对经对数转换的数据进行线性回归分析,同时对年龄和性别进行校正。
与对照组相比,霍奇金淋巴瘤患者的血清YKL-40和IL-6水平升高(YKL-40升高3.6倍;IL-6升高8.3倍;两者P均<0.0001)。在初治霍奇金淋巴瘤患者的治疗前样本(n = 176)中,其水平与更晚期别相关(趋势P值,YKL-40为0.0001,IL-6为0.013),在有B症状的患者中也是如此;然而,在结节硬化型和混合细胞型亚型中、按EBV状态、以及在较年轻(<45岁)和较年长患者中,水平相似。治疗开始后不久进行检测的患者水平显著低于治疗前患者;然而,即使在治疗开始后≥6个月,血清YKL-40和IL-6水平与对照组相比仍显著升高。在死亡患者(n = 12)中,YKL-40和IL-6的治疗前水平高于存活者,尽管无统计学显著性差异。
未治疗的霍奇金淋巴瘤患者以及更晚期别的患者血清YKL-40和IL-6水平升高,但在霍奇金淋巴瘤组织学类型之间无显著差异。治疗后,血清水平显著降低。