Dicuonzo Giordano, Vincenzi Bruno, Santini Daniele, Avvisati Giuseppe, Rocci Laura, Battistoni Fabrizio, Gavasci Michele, Borzomati Domenico, Coppola Roberto, Tonini Giuseppe
Università Campus Bio-Medico, Rome, Italy.
J Interferon Cytokine Res. 2003 Nov;23(11):649-54. doi: 10.1089/107999003322558782.
The most common adverse event typically associated with bisphosphonate therapy is transient fever. The aim of this study was to define the role of the main cytokines of the acute-phase reaction interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-alpha) involved in the pathogenesis of zoledronic acid-induced fever. Eighteen consecutive cancer patients with bone metastases were treated, for the first time, with a single dose of 4 mg zoledronic acid infusion. They were prospectively evaluated for circulating TNF-alpha, interferon-gamma (IFN-gamma), and IL-6 levels at different times, just before and 1, 2, 7, and 21 days after diphosphonate infusion. Clinical and standard laboratory parameters were recorded at the same time points. TNF-alpha circulating levels increased significantly 1 and 2 days after zoledronic acid infusion (respectively, p = 0.002 and p < 0.001) and then decreased to levels similar to the basal levels. IL-6 levels increased significantly 1 day after the infusion (p = 0.007), returning to values similar to the median basal values 2 days after zoledronic acid administration. Moreover, in patients who experienced fever, the TNF-alpha and IL-6 increases were higher than in patients without fever. No statistically significant differences in IFN-gamma were identified at different time points in patients with and without fever. Our results show that zoledronic acid induces transient TNF-alpha and IL-6 increases and that these increases are higher in patients who have developed fever, suggesting that these cytokines could be responsible for fever pathogenesis. The sharp reduction in serum calcium levels observed in patients with fever may be related to zoledronic acid pharmacokinetic modifications.
双膦酸盐治疗通常最常见的不良事件是短暂发热。本研究的目的是确定急性期反应的主要细胞因子白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)在唑来膦酸诱导发热的发病机制中所起的作用。连续18例有骨转移的癌症患者首次接受单剂量4mg唑来膦酸静脉输注治疗。在双膦酸盐输注前及输注后1、2、7和21天的不同时间点,对他们进行前瞻性评估,检测循环中的TNF-α、干扰素-γ(IFN-γ)和IL-6水平。同时记录临床和标准实验室参数。唑来膦酸输注后1天和2天,TNF-α循环水平显著升高(分别为p = 0.002和p < 0.001),然后降至与基础水平相似的水平。IL-6水平在输注后1天显著升高(p = 0.007),在唑来膦酸给药后2天恢复到与基础中位数水平相似的值。此外,在出现发热的患者中,TNF-α和IL-6的升高高于未发热的患者。在有发热和无发热的患者中,不同时间点的IFN-γ均未发现统计学上的显著差异。我们的结果表明,唑来膦酸可诱导TNF-α和IL-6短暂升高,且在发热患者中这些升高更为明显,提示这些细胞因子可能是发热发病机制的原因。发热患者血清钙水平的急剧下降可能与唑来膦酸的药代动力学改变有关。