Cargando…
Oxaliplatin‐ and docetaxel‐induced polyneuropathy: clinical and neurophysiological characteristics
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...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Periodicals, Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756561/ https://www.ncbi.nlm.nih.gov/pubmed/32902058 http://dx.doi.org/10.1111/jns.12413 |
_version_ | 1783626569735995392 |
---|---|
author | Bennedsgaard, Kristine Ventzel, Lise Andersen, Niels T. Themistocleous, Andreas C. Bennett, David L. Jensen, Troels S. Tankisi, Hatice Finnerup, Nanna B. |
author_facet | Bennedsgaard, Kristine Ventzel, Lise Andersen, Niels T. Themistocleous, Andreas C. Bennett, David L. Jensen, Troels S. Tankisi, Hatice Finnerup, Nanna B. |
author_sort | Bennedsgaard, Kristine |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7756561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wiley Periodicals, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77565612020-12-28 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. J Peripher Nerv Syst Research Reports 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. Wiley Periodicals, Inc. 2020-10-06 2020-12 /pmc/articles/PMC7756561/ /pubmed/32902058 http://dx.doi.org/10.1111/jns.12413 Text en © 2020 The Authors. Journal of the Peripheral Nervous System published by Wiley Periodicals LLC on behalf of Peripheral Nerve Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Reports Bennedsgaard, Kristine Ventzel, Lise Andersen, Niels T. Themistocleous, Andreas C. Bennett, David L. Jensen, Troels S. Tankisi, Hatice Finnerup, Nanna B. Oxaliplatin‐ and docetaxel‐induced polyneuropathy: clinical and neurophysiological characteristics |
title | Oxaliplatin‐ and docetaxel‐induced polyneuropathy: clinical and neurophysiological characteristics |
title_full | Oxaliplatin‐ and docetaxel‐induced polyneuropathy: clinical and neurophysiological characteristics |
title_fullStr | Oxaliplatin‐ and docetaxel‐induced polyneuropathy: clinical and neurophysiological characteristics |
title_full_unstemmed | Oxaliplatin‐ and docetaxel‐induced polyneuropathy: clinical and neurophysiological characteristics |
title_short | Oxaliplatin‐ and docetaxel‐induced polyneuropathy: clinical and neurophysiological characteristics |
title_sort | oxaliplatin‐ and docetaxel‐induced polyneuropathy: clinical and neurophysiological characteristics |
topic | Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756561/ https://www.ncbi.nlm.nih.gov/pubmed/32902058 http://dx.doi.org/10.1111/jns.12413 |
work_keys_str_mv | AT bennedsgaardkristine oxaliplatinanddocetaxelinducedpolyneuropathyclinicalandneurophysiologicalcharacteristics AT ventzellise oxaliplatinanddocetaxelinducedpolyneuropathyclinicalandneurophysiologicalcharacteristics AT andersennielst oxaliplatinanddocetaxelinducedpolyneuropathyclinicalandneurophysiologicalcharacteristics AT themistocleousandreasc oxaliplatinanddocetaxelinducedpolyneuropathyclinicalandneurophysiologicalcharacteristics AT bennettdavidl oxaliplatinanddocetaxelinducedpolyneuropathyclinicalandneurophysiologicalcharacteristics AT jensentroelss oxaliplatinanddocetaxelinducedpolyneuropathyclinicalandneurophysiologicalcharacteristics AT tankisihatice oxaliplatinanddocetaxelinducedpolyneuropathyclinicalandneurophysiologicalcharacteristics AT finnerupnannab oxaliplatinanddocetaxelinducedpolyneuropathyclinicalandneurophysiologicalcharacteristics |