4.2 Article

Long-term course of oxaliplatin-induced polyneuropathy: a prospective 2-year follow-up study

Journal

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
Volume 19, Issue 4, Pages 299-306

Publisher

WILEY-BLACKWELL
DOI: 10.1111/jns.12097

Keywords

chronic oxaliplatin-induced peripheral neuropathy; long-term course; neurotoxicity; oxaliplatin; Total Neuropathy Score (c) (TNS (c))

Funding

  1. ISCIII [PI070493]
  2. Fondazione G. Benzi

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This prospective study sought to identify the potential reversibility of oxaliplatin-induced peripheral neuropathy (OXAIPN) by following-up its long-term course 2 years after discontinuation of oxaliplatin (OXA)-based chemotherapy. Participants were 91 colorectal cancer patients treated with OXA-based chemotherapy. Neurological assessment, clinical Total Neuropathy Score(C) (TNSc(C)) and nerve conduction studies were performed at baseline (T0), the end of chemotherapy (T1) and 2 years (T2) after discontinuation of chemotherapy. A total of 73 of 91 (80%) patients experienced OXAIPN at T1. At a median follow-up of 25 months, persistence of chronic OXAIPN was present in 61 of 73 patients (84%) and complete resolution was present in 12 patients (17%). Longitudinal comparison of TNSc(C) values between T1 and T2 revealed that the overall severity of OXAIPN in those 61 patients significantly decreased over time. Median TNSc(C) values were nine (range: 2-15) at T1 vs. four (range: 2-12) at T2 (P<0.001). Likewise, sensory nerve conduction measures at T2 significantly improved in all sensory nerves tested, compared with T1. Severity of OXAIPN at T2 was significantly associated (P<0.001) with high severity of OXAIPN at T1. In conclusion, persistence of OXAIPN beyond 2 years after finishing chemotherapy is common. Clinical and neurophysiological improvement is observed, although recovery is often incomplete.

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