Department of Medical Oncology, City of Hope, 1500 East Duarte Road, Duarte, CA, 91010, USA,
J Neurooncol. 2014 May;118(1):169-77. doi: 10.1007/s11060-014-1415-4. Epub 2014 Mar 15.
Intracerebral microdialysis enables continuous measurement of changes in brain biochemistry. In this study intracerebral microdialysis was used to assess changes in cytokine levels after tumor resection and in response to treatment with temsirolimus. Brain tumor patients undergoing craniotomy participated in this non-therapeutic study. A 100 kDa molecular weight cut-off microdialysis catheter was placed in peritumoral tissue at the time of resection. Cohort 1 underwent craniotomy only. Cohort 2 received a 200 mg dose of intravenous temsirolimus 48 h after surgery. Dialysate samples were collected continuously for 96 h and analyzed for the presence of 30 cytokines. Serial blood samples were collected to measure systemic cytokine levels. Dialysate samples were obtained from six patients in cohort 1 and 4 in cohort 2. Seventeen cytokines could be recovered in dialysate samples from at least 8 of 10 patients. Concentrations of interleukins and chemokines were markedly elevated in peritumoral tissue, and most declined over time, with IL-8, IP-10, MCP-1, MIP1β, IL-6, IL-12p40/p70, MIP1α, IFN-α, G-CSF, IL-2R, and vascular endothelial growth factor significantly (p < 0.05) decreasing over 96 h following surgery. No qualitative changes in intracerebral or serum cytokine concentrations were detected after temsirolimus administration. This is the first intracerebral microdialysis study to evaluate the time course of changes in macromolecule levels in the peritumoral microenvironment after a debulking craniotomy. Initial elevations of peritumoral interleukins and chemokines most likely reflected an inflammatory response to both tumor and surgical trauma. These findings have implications for development of cellular therapies that are administered intracranially at the time of surgery.
脑室内微透析可连续测量脑生物化学变化。本研究采用脑室内微透析评估肿瘤切除后细胞因子水平的变化,并评估依维莫司治疗的效果。开颅手术的脑肿瘤患者参与了这项非治疗性研究。在切除时将 100kDa 分子量截止微透析导管置于肿瘤周围组织内。队列 1 仅接受开颅手术。队列 2 在手术后 48 小时给予 200mg 静脉注射依维莫司。连续 96 小时采集透析液样本,并分析 30 种细胞因子。采集系列血样以测量全身细胞因子水平。队列 1 获得 6 例患者和队列 2 4 例患者的透析液样本。至少有 10 例患者中的 8 例可从透析液样本中回收 17 种细胞因子。在肿瘤周围组织中白细胞介素和趋化因子的浓度明显升高,且大多数随时间下降,其中 IL-8、IP-10、MCP-1、MIP1β、IL-6、IL-12p40/p70、MIP1α、IFN-α、G-CSF、IL-2R 和血管内皮生长因子在手术后 96 小时内显著(p<0.05)下降。依维莫司给药后未检测到脑内或血清细胞因子浓度的定性变化。这是第一项评估肿瘤切除后肿瘤周围微环境中大分子水平变化时间过程的脑室内微透析研究。初始肿瘤周围白细胞介素和趋化因子升高可能反映了肿瘤和手术创伤的炎症反应。这些发现对手术时颅内给予细胞治疗的发展具有重要意义。