Department of Health Policy & Management, UCLA Fielding School of Public Health, Los Sangeles, CA, USA.
Brain Behav Immun. 2013 Mar;30 Suppl(Suppl):S99-108. doi: 10.1016/j.bbi.2012.07.015. Epub 2012 Aug 3.
Post-chemotherapy treated cancer patients frequently report cognitive difficulties. The biology of this phenomenon is poorly understood, with uncertainty about possible direct toxic effects on the brain, secondary effects from systemic inflammation, host factors/genetic predisposition to cognitive complaints, or hormonal changes influencing cognitive function. To elucidate possible mechanisms associated with post-treatment cognitive dysfunction among breast cancer survivors, in 2007 we established a prospective, longitudinal, observational cohort study of early stage breast cancer patients, recruited at the end of initial treatments (primary treatment exposure included surgery, ± radiation, ± chemotherapy), and prior to the initiation of adjuvant endocrine therapy. We assessed cognitive complaints, neuropsychological (NP) test performance, markers of inflammation, and brain imaging at baseline, 6 months and 12 months after enrollment. In this analysis of data from the first 93 patients enrolled in the cohort study, we focus on the relationship of circulating levels of proinflammatory cytokines to cerebral functioning and chemotherapy exposure. Among the proinflammatory cytokines tested (IL-1 ra, sTNF-RII, CRP, and IL-6) at baseline, only sTNF-RII was increased among chemotherapy exposed patients, with a significant decline in the year after treatment (p=0.003). Higher baseline sTNF-RII in chemotherapy patients was significantly associated with increased memory complaints. In chemotherapy exposed patients, the longitudinal decline in sTNF-RII was significantly correlated with fewer memory complaints over 12 months (r=-0.34, p=0.04). Higher baseline sTNF-RII was also associated with relatively diminished brain metabolism in the inferior frontal cortex (r=-0.55, p=0.02), as well as relatively increased inferior frontal metabolism after 1 year, in chemotherapy-exposed subjects. These preliminary findings suggest that post-chemotherapy increases in TNF-α may be playing an important role in the manifestations of cognitive complaints in breast cancer survivors.
化疗后治疗的癌症患者经常报告认知困难。这种现象的生物学机制尚未得到充分理解,可能存在对大脑的直接毒性作用、全身炎症的继发影响、认知症状的宿主因素/遗传易感性或影响认知功能的激素变化等不确定因素。为了阐明乳腺癌幸存者治疗后认知功能障碍的可能机制,我们于 2007 年建立了一项前瞻性、纵向、观察性队列研究,纳入了初始治疗结束时(主要治疗暴露包括手术、±放疗、±化疗)且在辅助内分泌治疗开始之前的早期乳腺癌患者。我们在基线、入组后 6 个月和 12 个月评估认知症状、神经心理学(NP)测试表现、炎症标志物和脑成像。在对该队列研究中前 93 名患者的数据进行的这项分析中,我们重点关注循环促炎细胞因子与大脑功能和化疗暴露的关系。在基线时检测的促炎细胞因子(IL-1 ra、sTNF-RII、CRP 和 IL-6)中,仅 sTNF-RII 在接受化疗的患者中增加,且在治疗后 1 年内显著下降(p=0.003)。化疗患者的基线 sTNF-RII 较高与记忆症状增加显著相关。在接受化疗的患者中,sTNF-RII 的纵向下降与 12 个月内记忆症状减少显著相关(r=-0.34,p=0.04)。较高的基线 sTNF-RII 还与额下回皮质的脑代谢相对减少相关(r=-0.55,p=0.02),以及化疗暴露后受试者 1 年后额下回代谢相对增加相关。这些初步发现表明,化疗后 TNF-α 的增加可能在乳腺癌幸存者认知症状的表现中起着重要作用。