Departments of Neurology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Neurology. 2011 Sep 6;77(10):980-6. doi: 10.1212/WNL.0b013e31822cfc59. Epub 2011 Aug 24.
To characterize the natural history of oxaliplatin-associated neuropathy (ON) and determine whether intraepidermal nerve fiber density (IENFD) is a sensitive measure of neuropathy progression. In addition, we sought to assess the potential of ON as a neuroprotection model and gain insight into the relationship between axon loss and neuropathic symptoms.
Eight subjects receiving oxaliplatin for advanced colorectal cancer were prospectively followed prior to starting chemotherapy and at 30, 90, 180, and 360 days (180 days after completing treatment). Electrophysiology, punch biopsies, symptom assessment, and examinations with calculation of a reduced total neuropathy score (rTNS) were performed at each time point. Changes over time were assessed through Poisson regression for IENFD and a mixed effects model for rTNS and electrophysiology measures.
The distal leg IENFD, rTNS, peroneal, and sural amplitudes were all significantly reduced over time, while conduction velocity (peroneal and sural) and distal thigh IENFD were not. Measures of axon loss continued to worsen following discontinuation of oxaliplatin. Five of 8 subjects reported prominent symptoms associated with oxaliplatin administration.
This study demonstrates that oxaliplatin is associated with mild, sensory, and motor axon loss that may not be reversible. Axonal loss was detected by electrophysiology, rTNS, and distal leg IENFD. Several subjects reported prominent sensory symptoms that were not associated with axon loss, and that may or may not represent neuropathy. ON is an attractive paradigm for neuroprotection studies and the distal leg IENFD is an objective measure that requires minimal subject participation or study site expertise.
描述奥沙利铂相关神经病变(ON)的自然病程,并确定表皮内神经纤维密度(IENFD)是否是神经病变进展的敏感指标。此外,我们还试图评估 ON 作为神经保护模型的潜力,并深入了解轴突丢失与神经症状之间的关系。
8 例接受奥沙利铂治疗晚期结直肠癌的患者在开始化疗前和 30、90、180 和 360 天(治疗结束后 180 天)进行前瞻性随访。在每个时间点进行电生理学、活检、症状评估以及计算简化总神经病变评分(rTNS)的检查。通过泊松回归评估 IENFD 的时间变化,并通过混合效应模型评估 rTNS 和电生理学测量的时间变化。
远端腿部 IENFD、rTNS、腓肠和腓总神经的振幅均随时间显著降低,而腓肠和腓总神经的传导速度(distal thigh IENFD)则没有。奥沙利铂停用后,轴突丢失的测量值仍继续恶化。8 例中有 5 例报告了奥沙利铂给药后明显的症状。
本研究表明奥沙利铂与轻度、感觉和运动轴突丢失有关,且可能无法恢复。轴突丢失通过电生理学、rTNS 和远端腿部 IENFD 检测到。一些患者报告了明显的感觉症状,但与轴突丢失无关,这些症状可能代表也可能不代表神经病变。ON 是神经保护研究的一个有吸引力的范例,而远端腿部 IENFD 是一种客观的测量方法,需要最少的受试者参与或研究场所的专业知识。