Oxaliplatin-induced Acute Neurotoxicity Recovers Between Repeat Infusion Cycles: An Axonal Excitability Repeated Multiple Measurements Study.

Cancer diagnosis & prognosis Pub Date : 2024-05-03 eCollection Date: 2024-05-01 DOI:10.21873/cdp.10327
Panagiotis Kokotis, Michail Papantoniou, Richard W Carr, Martin Schmelz, Dimitra Siakavella, Efthymia Skafida, Christos Papadimitriou
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Abstract

Background/aim: Oxaliplatin, a platinum-based chemotherapy used in the treatment of colorectal cancer, induces acute neurotoxicity following infusion. The aim of this study was to establish whether alterations in axonal excitability develop progressively with higher cumulative doses and whether there is a recovery in motor axons after each cycle of treatment.

Patients and methods: Twenty consecutive patients with a colorectal cancer diagnosis, referred from the Oncology Department of Aretaieion Hospital of Athens, were enrolled in this study between October 2018 and May 2019. None of the participants had diabetes, alcohol abuse, known neuropathy or were previously treated with another neo-adjuvant therapy. Threshold Tracking techniques and Qtrac software were used for assessing axonal excitability in motor axons. Excitability recordings were undertaken before and immediately after the end of oxaliplatin infusion.

Results: Statistically significant changes were found (p<0.01) in axonal excitability (relative refractory period, refractoriness at 2 ms and 2.5 ms, sub-excitability and super-excitability) before and after oxaliplatin infusion. No statistically significant changes (p>0.05) were found in threshold electrotonus and strength-duration parameters before and after oxaliplatin infusion. We also did not find statistically significant differences (p>0.05) between means of excitability parameters before infusion at each cycle.

Conclusion: Our study confirms oxaliplatin-induced acute neurotoxicity following infusion and suggests that motor axons recover between repeat infusion cycles.

奥沙利铂诱导的急性神经毒性可在重复输注周期之间恢复:轴突兴奋性重复多次测量研究》。
背景/目的:奥沙利铂是一种用于治疗结直肠癌的铂类化疗药物,输注后会诱发急性神经毒性。本研究旨在确定轴突兴奋性的改变是否会随着累积剂量的增加而逐渐发展,以及运动轴突是否会在每个治疗周期后恢复:2018年10月至2019年5月期间,雅典Aretaieion医院肿瘤科转诊的连续20名结肠直肠癌患者被纳入本研究。所有参与者均无糖尿病、酗酒、已知神经病变或曾接受过其他新辅助疗法。阈值跟踪技术和Qtrac软件用于评估运动轴突的轴突兴奋性。在奥沙利铂输注前和输注结束后立即进行兴奋性记录:结果:在输注奥沙利铂前后,阈值电通量和强度-持续时间参数发生了统计学意义上的重大变化(P0.05)。我们也没有发现输注前每个周期的兴奋性参数平均值之间存在统计学意义上的显著差异(P>0.05):我们的研究证实了奥沙利铂诱导的输注后急性神经毒性,并表明运动轴突在重复输注周期之间可以恢复。
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