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Oxaliplatin- and docetaxel-induced polyneuropathy: clinical and neurophysiological characteristics.
Bennedsgaard, Kristine; Ventzel, Lise; Andersen, Niels T; Themistocleous, Andreas C; Bennett, David L; Jensen, Troels S; Tankisi, Hatice; Finnerup, Nanna B.
Affiliation
  • Bennedsgaard K; Danish Pain Research Center, Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
  • Ventzel L; Danish Pain Research Center, Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
  • Andersen NT; Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
  • Themistocleous AC; Biostatistics, Department of Public Health, Aarhus University, Aarhus, Denmark.
  • Bennett DL; Nuffield Department of Clinical Neuroscience, University of Oxford, UK.
  • Jensen TS; Brain Function Research Group, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
  • Tankisi H; Nuffield Department of Clinical Neuroscience, University of Oxford, UK.
  • Finnerup NB; Danish Pain Research Center, Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
J Peripher Nerv Syst ; 25(4): 377-387, 2020 12.
Article in En | MEDLINE | ID: mdl-32902058
ABSTRACT
The aim of this study was to evaluate the presence and characterization of chemotherapy-induced neuropathy (CIPN) and neuropathic pain 5 years after adjuvant chemotherapy with docetaxel or oxaliplatin. Patients from an ongoing prospective study, who had received adjuvant chemotherapy with docetaxel or oxaliplatin in 2011 to 2012 were invited to participate. The patients underwent a thorough examination with interview, neurological examination, questionnaires, assessment tools, nerve conduction studies (NCS), quantitative sensory testing, MScan motor unit number estimation (MUNE), and corneal confocal microscopy (CCM). Patients were divided into no, possible, probable, and confirmed CIPN. Out of the 132 eligible patients, 63 agreed to participate 28 had received docetaxel and 35 had received oxaliplatin. Forty-one percent had confirmed CIPN, 34% possible or probable CIPN, and 22% did not have CIPN. The CIPN was characterized mainly by sensory nerve fiber loss, with a more pronounced large fiber than small fiber loss but also some motor fiber loss identified on NCS and MUNE. In general, patients had mild neuropathy with relatively low scores on assessment tools and no association with mood and quality of life. CCM was not useful as a diagnostic tool. Of the patients with probable or confirmed CIPN, 30% experienced pain, which was most often mild, but still interfered moderately with daily life in 20% to 25% and was associated with lower quality of life. In conclusion CIPN was confirmed in 41% 5 years after chemotherapy. The neuropathy was generally mild, but in patients with neuropathic pain it was associated with lower quality of life.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polyneuropathies / Severity of Illness Index / Diagnostic Techniques, Neurological / Docetaxel / Oxaliplatin / Neoplasms / Antineoplastic Agents Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: J Peripher Nerv Syst Journal subject: NEUROLOGIA Year: 2020 Document type: Article Affiliation country: Dinamarca

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polyneuropathies / Severity of Illness Index / Diagnostic Techniques, Neurological / Docetaxel / Oxaliplatin / Neoplasms / Antineoplastic Agents Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: J Peripher Nerv Syst Journal subject: NEUROLOGIA Year: 2020 Document type: Article Affiliation country: Dinamarca
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