Division of Medical Oncology and Molecular Respirology, Faculty of Medicine, Tottori University, 36-1, Nishi-machi, Yonago, 683-8504, Japan.
Lung Cancer. 2018 Aug;122:200-205. doi: 10.1016/j.lungcan.2018.06.022. Epub 2018 Jun 18.
Zoledronate (ZOL) is usually used for prevention of skeletal-related events in cancer patients with bone metastases. The first administration of ZOL is occasionally associated with development of acute-phase reaction (APR), which is due to activation of γδ T cells. ZOL-related APR was associated with better overall survival (OS) of patients with non-small cell lung cancer (NSCLC) in our previous retrospective study. However, it remains to be clarified whether γδ T cells are more activated in patients who experienced ZOL-related APR, and whether γδ T cell activation is involved in prolongation of OS.
Twenty-three patients with advanced NSCLC were recruited between 2012 and 2014 in this study. We administered ZOL to participants with standard care. The patient characteristics, change in γδ T cell counts and cytokines, OS, and skeletal-related event-free survival were compared between patients with APR (APR group) and those without APR (non-APR group).
Ten patients (43.5%) experienced a ZOL-related APR. The number of γδ T cells at baseline in the APR group was significantly higher than that in the non-APR group. Serum interleukin-6 and tumor necrosis factor-α in the APR group were significantly increased, but no change in the number of γδ T cells was observed after the first administration of ZOL in both groups. OS in the APR group was significantly longer than that in the non-APR group (median survival time: 23.1 vs. 14.5 months, p < 0.01).
We showed that APR is related to higher numbers of γδ T cells at baseline and increased cytokines after the first ZOL administration, but not to proliferative responses of γδ T cells. In addition, better OS was observed in the APR group. Therefore, the number of γδ T cells might be a prognostic marker in patients with NSCLC.
唑来膦酸(ZOL)通常用于预防有骨转移的癌症患者的骨骼相关事件。ZOL 的首次给药偶尔会引起急性期反应(APR),这是由于 γδ T 细胞的激活。我们之前的回顾性研究表明,ZOL 相关的 APR 与非小细胞肺癌(NSCLC)患者的总生存(OS)更好相关。然而,γδ T 细胞在经历 ZOL 相关 APR 的患者中是否更活跃,以及 γδ T 细胞的激活是否参与 OS 的延长,仍有待阐明。
本研究纳入了 2012 年至 2014 年期间的 23 例晚期 NSCLC 患者。我们按标准护理给参与者施用 ZOL。比较了有 APR(APR 组)和无 APR(非 APR 组)的患者的患者特征、γδ T 细胞计数和细胞因子的变化、OS 和骨骼相关事件无进展生存。
10 例患者(43.5%)经历了 ZOL 相关的 APR。APR 组的基线 γδ T 细胞数量明显高于非 APR 组。APR 组的血清白细胞介素 6 和肿瘤坏死因子-α显著增加,但两组中 ZOL 首次给药后 γδ T 细胞数量均无变化。APR 组的 OS 明显长于非 APR 组(中位生存时间:23.1 与 14.5 个月,p < 0.01)。
我们表明,APR 与基线时 γδ T 细胞数量较高和首次 ZOL 给药后细胞因子增加有关,但与 γδ T 细胞的增殖反应无关。此外,APR 组的 OS 更好。因此,γδ T 细胞的数量可能是非小细胞肺癌患者的预后标志物。