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Long‐term course of oxaliplatin‐induced polyneuropathy: a prospective 2‐year follow‐up study
Authors:Chiara Briani  Andreas A. Argyriou  Cristina Izquierdo  Roser Velasco  Marta Campagnolo  Paola Alberti  Barbara Frigeni  Mario Cacciavillani  Francesca Bergamo  Diego Cortinovis  Marina Cazzaniga  Jordi Bruna  Guido Cavaletti  Haralabos P. Kalofonos
Affiliation:1. Department of Neurosciences, Sciences NPSRR, University of Padova, , Padova, Italy;2. Department of Neurology, “Saint Andrew's” State General Hospital of Patras, , Patras, Greece;3. Department of Medicine, Division of Clinical Oncology, University Hospital of Patras, , Rion‐Patras, Greece;4. Unit of Neuro‐Oncology, Hospital Universitari de Bellvitge‐ICO Duran i Reynals, , Barcelona, Spain;5. Department of Surgery and Translational Medicine, University of Milan‐Bicocca, , Monza, Italy;6. CEMES, EMG Unit, Data Medica Group, , Padova, Italy;7. Istituto Oncologico Veneto, IRCCS, , Padova, Italy;8. Department of Oncology, S. Gerardo Hospital, , Monza, Italy
Abstract: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© (TNSc©) 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© values between T1 and T2 revealed that the overall severity of OXAIPN in those 61 patients significantly decreased over time. Median TNSc© 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.
Keywords:chronic oxaliplatin‐induced peripheral neuropathy  long‐term course  neurotoxicity  oxaliplatin  Total Neuropathy Score©   (TNS©  )
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