Gehr Nina Lykkegaard, Mortensen Christina, Stage Tore B, Pedersen Malene Roland Vils, Rafaelsen Søren Rafael, Madsen Jonna Skov, Olsen Dorte Aalund, Timm Signe, Jensen Lars Henrik, Hansen Torben Frøstrup, Finnerup Nanna Brix, Ventzel Lise
Danish Pain Research Center, Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Department of Oncology, University Hospital of Southern Denmark, Vejle, Denmark.
Cancer Chemother Pharmacol. 2025 Apr 10;95(1):53. doi: 10.1007/s00280-025-04773-w.
Oxaliplatin-induced peripheral neuropathy (OIPN) is a chronic, debilitating late effect following oxaliplatin treatment. Neurofilament light chain (NfL) is a structural protein found in nerve axons that was investigated upon oxaliplatin exposure in vitro and in vivo correlated to symptoms of OIPN in colorectal cancer patients receiving oxaliplatin.
Human sensory neurons, derived from induced pluripotent stem cells, were exposed to clinically relevant concentrations of oxaliplatin in vitro, with NfL concentrations measured in the cell medium. The prospective clinical study included patients with colorectal cancer undergoing chemotherapy therapy with or without oxaliplatin. Possible OIPN was defined as bilateral presence of numbness and/or presence of pricking sensations in the feet documented in an interview at the time of blood sampling prior to, 3, and 6 months after initiating treatment.
Oxaliplatin exposure led to a dose-dependent NfL increase in vitro. In the clinical cohort of 30 patients (18 in the oxaliplatin group), NfL levels rose at 3 and 6 months compared to controls. NfL level changes correlated to OIPN symptoms at the 6-month timepoint (rho 0.81, p < 0.001). However, the interindividual variation was substantial, and most patients showed only a minor increase in NfL.
Both in vitro and clinical data indicate that oxaliplatin exposure results in elevated NfL levels. Further prospective studies are needed to evaluate NfL as an early biomarker for OIPN, specifically focusing on the timing of blood sampling during chemotherapy treatment to enable the timely reduction of oxaliplatin.
奥沙利铂诱导的周围神经病变(OIPN)是奥沙利铂治疗后的一种慢性、使人衰弱的迟发效应。神经丝轻链(NfL)是一种存在于神经轴突中的结构蛋白,在体外和体内对其进行了研究,以探讨其与接受奥沙利铂治疗的结直肠癌患者OIPN症状的相关性。
将源自诱导多能干细胞的人感觉神经元在体外暴露于临床相关浓度的奥沙利铂,并测量细胞培养基中的NfL浓度。前瞻性临床研究纳入了接受含或不含奥沙利铂化疗的结直肠癌患者。可能的OIPN定义为在开始治疗前、治疗3个月和6个月时采血时通过访谈记录到的双脚双侧麻木和/或刺痛感。
体外奥沙利铂暴露导致NfL呈剂量依赖性增加。在30例患者的临床队列中(奥沙利铂组18例),与对照组相比,NfL水平在3个月和6个月时升高。NfL水平变化与6个月时的OIPN症状相关(rho 0.81,p<0.001)。然而,个体间差异很大,大多数患者的NfL仅略有增加。
体外和临床数据均表明,奥沙利铂暴露会导致NfL水平升高。需要进一步的前瞻性研究来评估NfL作为OIPN的早期生物标志物,特别关注化疗期间采血的时间,以便及时减少奥沙利铂的用量。