Chemotherapy-Induced Peripheral Neuropathy: Mechanisms and Therapeutic Avenues

被引:64
作者
Bae, Esther H. [1 ]
Greenwald, Mark K. [1 ,2 ]
Schwartz, Ann G. [1 ,2 ]
机构
[1] Wayne State Univ, Dept Psychiat & Behav Neurosci, Sch Med, 3901 Chrysler Serv Dr,Suite 2A, Detroit, MI 48201 USA
[2] Karmanos Canc Inst, Detroit, MI USA
关键词
Chemotherapy-induced peripheral neuropathy; Mechanisms; Treatment; Neuroprotective; Antinociceptive; OXALIPLATIN-INDUCED NEUROPATHY; PACLITAXEL-INDUCED NEUROPATHY; RECEPTOR ANTAGONIST; TUBULIN POLYMERIZATION; OXIDATIVE STRESS; CLINICAL-TRIALS; DOUBLE-BLIND; PAIN RELIEF; CANNABIDIOL; INHIBITION;
D O I
10.1007/s13311-021-01142-2
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Chemotherapy-induced peripheral neuropathy (CIPN) is a serious and often persistent adverse consequence of certain chemotherapeutic agents. It is a major dose-limiting factor of many first-line chemotherapies, affecting 20-50% of patients at standard doses and nearly all patients at high doses. As cancer survivorship continues to increase with improvements in early diagnosis and treatment, more patients will experience CIPN despite completing cancer treatment, which interferes with recovery, leading to chronic pain and worsening quality of life. The National Cancer Institute has identified CIPN as a priority in translational research. To date, there are no FDA-approved drugs for preventing or treating CIPN, with emerging debate on mechanisms and promising new targets. This review highlights current literature and suggests novel approaches to CIPN based on proposed mechanisms of action that aim either to confer neuroprotection against chemotherapy-induced neurotoxicity or reverse the downstream effects of painful neuropathy.
引用
收藏
页码:2384 / 2396
页数:13
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