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Neurofilament proteins as a potential biomarker in chemotherapy-induced polyneuropathy
BACKGROUND: Paclitaxel chemotherapy frequently induces dose-limiting sensory axonal polyneuropathy. Given that sensory symptoms are challenging to assess objectively in clinical practice, an easily accessible biomarker for chemotherapy-induced polyneuropathy (CIPN) holds the potential to improve ear...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986065/ https://www.ncbi.nlm.nih.gov/pubmed/35133982 http://dx.doi.org/10.1172/jci.insight.154395 |
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author | Huehnchen, Petra Schinke, Christian Bangemann, Nikola Dordevic, Adam D. Kern, Johannes Maierhof, Smilla K. Hew, Lois Nolte, Luca Körtvelyessy, Peter Göpfert, Jens C. Ruprecht, Klemens Somps, Christopher J. Blohmer, Jens-Uwe Sehouli, Jalid Endres, Matthias Boehmerle, Wolfgang |
author_facet | Huehnchen, Petra Schinke, Christian Bangemann, Nikola Dordevic, Adam D. Kern, Johannes Maierhof, Smilla K. Hew, Lois Nolte, Luca Körtvelyessy, Peter Göpfert, Jens C. Ruprecht, Klemens Somps, Christopher J. Blohmer, Jens-Uwe Sehouli, Jalid Endres, Matthias Boehmerle, Wolfgang |
author_sort | Huehnchen, Petra |
collection | PubMed |
description | BACKGROUND: Paclitaxel chemotherapy frequently induces dose-limiting sensory axonal polyneuropathy. Given that sensory symptoms are challenging to assess objectively in clinical practice, an easily accessible biomarker for chemotherapy-induced polyneuropathy (CIPN) holds the potential to improve early diagnosis. Here, we describe neurofilament light chain (NFL), a marker for neuroaxonal damage, as a translational surrogate marker for CIPN. METHODS: NFL concentrations were measured in an in vitro model of CIPN, exposing induced pluripotent stem cell–derived sensory neurons (iPSC-DSNs) to paclitaxel. Patients with breast or ovarian cancer undergoing paclitaxel chemotherapy, breast cancer control patients without chemotherapy, and healthy controls were recruited in a cohort study and examined before chemotherapy (V1) and after 28 weeks (V2, after chemotherapy). CIPN was assessed by the validated Total Neuropathy Score reduced (TNSr), which combines patient-reported symptoms with data from clinical examinations. Serum NFL (NFL(s)) concentrations were measured at both visits with single-molecule array technology. RESULTS: NFL was released from iPSC-DSNs upon paclitaxel incubation in a dose- and time-dependent manner and was inversely correlated with iPSC-DSN viability. NFL(s) strongly increased in paclitaxel-treated patients with CIPN, but not in patients receiving chemotherapy without CIPN or controls, resulting in an 86% sensitivity and 87% specificity. An NFL(s) increase of +36 pg/mL from baseline was associated with a predicted CIPN probability of more than 0.5. CONCLUSION: NFL(s) was correlated with CIPN development and severity, which may guide neurotoxic chemotherapy in the future. TRIAL REGISTRATION: ClinicalTrials.gov NCT02753036. FUNDING: Deutsche Forschungsgemeinschaft (EXC 257 NeuroCure), BMBF (Center for Stroke Research Berlin, 01 EO 0801), Animalfree Research, EU Horizon 2020 Innovative Medicines Initiative 2 Joint Undertaking (TransBioLine, 821283), Charité 3R — Replace — Reduce — Refine. |
format | Online Article Text |
id | pubmed-8986065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-89860652022-04-07 Neurofilament proteins as a potential biomarker in chemotherapy-induced polyneuropathy Huehnchen, Petra Schinke, Christian Bangemann, Nikola Dordevic, Adam D. Kern, Johannes Maierhof, Smilla K. Hew, Lois Nolte, Luca Körtvelyessy, Peter Göpfert, Jens C. Ruprecht, Klemens Somps, Christopher J. Blohmer, Jens-Uwe Sehouli, Jalid Endres, Matthias Boehmerle, Wolfgang JCI Insight Clinical Medicine BACKGROUND: Paclitaxel chemotherapy frequently induces dose-limiting sensory axonal polyneuropathy. Given that sensory symptoms are challenging to assess objectively in clinical practice, an easily accessible biomarker for chemotherapy-induced polyneuropathy (CIPN) holds the potential to improve early diagnosis. Here, we describe neurofilament light chain (NFL), a marker for neuroaxonal damage, as a translational surrogate marker for CIPN. METHODS: NFL concentrations were measured in an in vitro model of CIPN, exposing induced pluripotent stem cell–derived sensory neurons (iPSC-DSNs) to paclitaxel. Patients with breast or ovarian cancer undergoing paclitaxel chemotherapy, breast cancer control patients without chemotherapy, and healthy controls were recruited in a cohort study and examined before chemotherapy (V1) and after 28 weeks (V2, after chemotherapy). CIPN was assessed by the validated Total Neuropathy Score reduced (TNSr), which combines patient-reported symptoms with data from clinical examinations. Serum NFL (NFL(s)) concentrations were measured at both visits with single-molecule array technology. RESULTS: NFL was released from iPSC-DSNs upon paclitaxel incubation in a dose- and time-dependent manner and was inversely correlated with iPSC-DSN viability. NFL(s) strongly increased in paclitaxel-treated patients with CIPN, but not in patients receiving chemotherapy without CIPN or controls, resulting in an 86% sensitivity and 87% specificity. An NFL(s) increase of +36 pg/mL from baseline was associated with a predicted CIPN probability of more than 0.5. CONCLUSION: NFL(s) was correlated with CIPN development and severity, which may guide neurotoxic chemotherapy in the future. TRIAL REGISTRATION: ClinicalTrials.gov NCT02753036. FUNDING: Deutsche Forschungsgemeinschaft (EXC 257 NeuroCure), BMBF (Center for Stroke Research Berlin, 01 EO 0801), Animalfree Research, EU Horizon 2020 Innovative Medicines Initiative 2 Joint Undertaking (TransBioLine, 821283), Charité 3R — Replace — Reduce — Refine. American Society for Clinical Investigation 2022-03-22 /pmc/articles/PMC8986065/ /pubmed/35133982 http://dx.doi.org/10.1172/jci.insight.154395 Text en © 2022 Huehnchen et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Clinical Medicine Huehnchen, Petra Schinke, Christian Bangemann, Nikola Dordevic, Adam D. Kern, Johannes Maierhof, Smilla K. Hew, Lois Nolte, Luca Körtvelyessy, Peter Göpfert, Jens C. Ruprecht, Klemens Somps, Christopher J. Blohmer, Jens-Uwe Sehouli, Jalid Endres, Matthias Boehmerle, Wolfgang Neurofilament proteins as a potential biomarker in chemotherapy-induced polyneuropathy |
title | Neurofilament proteins as a potential biomarker in chemotherapy-induced polyneuropathy |
title_full | Neurofilament proteins as a potential biomarker in chemotherapy-induced polyneuropathy |
title_fullStr | Neurofilament proteins as a potential biomarker in chemotherapy-induced polyneuropathy |
title_full_unstemmed | Neurofilament proteins as a potential biomarker in chemotherapy-induced polyneuropathy |
title_short | Neurofilament proteins as a potential biomarker in chemotherapy-induced polyneuropathy |
title_sort | neurofilament proteins as a potential biomarker in chemotherapy-induced polyneuropathy |
topic | Clinical Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986065/ https://www.ncbi.nlm.nih.gov/pubmed/35133982 http://dx.doi.org/10.1172/jci.insight.154395 |
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