Rhee John Y, Paulino Maria T, Finnemore Alexander, Tentor Zachary, Cashman Christopher
Center for Neuro-Oncology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Division of Adult Palliative Care, Department of Supportive Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Curr Neurol Neurosci Rep. 2025 Jun 20;25(1):42. doi: 10.1007/s11910-025-01429-3.
The purpose of this article is to provide an update on cancer-related neuropathies over the past five years, by reviewing the advances in pathophysiology and biology, diagnostic approaches, and management strategies.
New agents causing peripheral neuropathy include antibody-drug conjugates, combinations of immune-checkpoint inhibitor therapies, and targeted therapies. Development of axonal neuropathies has been found to be mediated through the protein sterile-α and Toll/interleukin 1 receptor motif containing protein 1 (SARM1). There have been emerging imaging modalities such as high-field MRI and neuromuscular ultrasound, and serum biomarkers, such as neurofilament light chain and glial fibrillary acid protein. Though calmangafodipir was negative for preventing peripheral neuropathy in oxaliplatin-based treatments, the POLAR trial randomizing patients to cooling or compression of the dominant hand during taxane administration significantly reduced incidence of chemotherapy-induced peripheral neuropathy. As of yet, there are no treatments for chemotherapy-induced peripheral neuropathy, but continued basic research into the SARM pathway is likely to yield novel agents that will stop, or prevent, the process.
本文旨在通过回顾过去五年癌症相关神经病变在病理生理学、生物学、诊断方法及管理策略方面的进展,提供最新信息。
导致周围神经病变的新药物包括抗体药物偶联物、免疫检查点抑制剂联合疗法及靶向疗法。已发现轴索性神经病变的发生是由含蛋白无菌α和Toll/白细胞介素1受体基序蛋白1(SARM1)介导的。出现了诸如高场MRI和神经肌肉超声等新兴成像方式,以及血清生物标志物,如神经丝轻链和胶质纤维酸性蛋白。尽管钙锰双吡啶在基于奥沙利铂的治疗中预防周围神经病变呈阴性,但将患者随机分为紫杉烷给药期间优势手冷却或加压组的POLAR试验显著降低了化疗引起的周围神经病变的发生率。目前,化疗引起的周围神经病变尚无治疗方法,但对SARM途径的持续基础研究可能会产生能够阻止该过程的新型药物。