Chemotherapy-induced polyneuropathy: diagnostic challenges and the potential of neurofilament as a biomarker for sensory disorders: the CONKO 023-ChemTox Trial

Chemotherapy-induced polyneuropathy (CIPN) is a prevalent side effect impairing patients' quality of life, often manifesting as dysesthesia or pain in extremities. To minimize therapy-related side effects as well as to improve quality of life, modern approaches grow increasingly more relevant. We conducted a longitudinal, prospective study to examine patients with lymphoma, leukemia, or gastrointestinal malignancies receiving continuous and temporary treatment up to five times over a 12- to 24-month period, beginning prior to chemotherapy. Assessments included comprehensive questionnaires, clinical neurological and electroneurographic examinations and measurements of neurofilament light chain (NFL). One hundred eight patients were enrolled with fifty-six patients having undergone all examinations both before and after chemotherapy. Data showed a significant rise of the mean Total Neuropathy Score (TNSr) after chemotherapy. Results revealed that approximately 75% of patients experienced CIPN. Continuous chemotherapy was associated with a steady increase in TNSr. Older patients, often with pre-existing and underdiagnosed neuropathy, were more frequently and more severely affected. According to medical records, where diagnostics were primarily based on patients' subjective information, even moderate cases were frequently underdiagnosed. A moderate correlation was observed between the increase in NfL and changes in TNSr (r = 0.385, p = 0.004). Patients with cancer affecting the central nervous system (CNS) showed elevated baseline NFL levels. In contrast to non-responders, NFL decreased in patients who responded well to therapy. In conclusion, data underline the necessity of improved diagnostic accuracy of CIPN and support the potential of NFL as a biomarker for its detection. Further investigations should assess its potential in daily oncological routine.Trial registration number: EA2/167/21 (date of registration: 12.08.2021).

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Publication Details

Journal
Journal of Neurology
Published
2025-10-22
DOI
https://doi.org/10.1007/s00415-025-13463-9
Primary Topic
Cancer Treatment and Pharmacology
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article
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article

Chemotherapy-induced polyneuropathy: diagnostic challenges and the potential of neurofilament as a biomarker for sensory disorders: the CONKO 023-ChemTox Trial

Uwe Pelzer, Sebastian Stintzing, Sebastian Schröder, Wolfgang Boehmerle et al.
Journal of Neurology
Cancer Treatment and Pharmacology
article

Chemotherapy-induced polyneuropathy: diagnostic challenges and the potential of neurofilament as a biomarker for sensory disorders: the CONKO 023-ChemTox Trial

Uwe Pelzer, Sebastian Stintzing, Sebastian Schröder, Wolfgang Boehmerle, Soo Ann Yap, Nigel Dross Engelbert Schaeper, Tobias Bleumer, Janine Abel, Lars Uwe Stephan
article en

Abstract

Chemotherapy-induced polyneuropathy (CIPN) is a prevalent side effect impairing patients' quality of life, often manifesting as dysesthesia or pain in extremities. To minimize therapy-related side effects as well as to improve quality of life, modern approaches grow increasingly more relevant. We conducted a longitudinal, prospective study to examine patients with lymphoma, leukemia, or gastrointestinal malignancies receiving continuous and temporary treatment up to five times over a 12- to 24-month period, beginning prior to chemotherapy. Assessments included comprehensive questionnaires, clinical neurological and electroneurographic examinations and measurements of neurofilament light chain (NFL). One hundred eight patients were enrolled with fifty-six patients having undergone all examinations both before and after chemotherapy. Data showed a significant rise of the mean Total Neuropathy Score (TNSr) after chemotherapy. Results revealed that approximately 75% of patients experienced CIPN. Continuous chemotherapy was associated with a steady increase in TNSr. Older patients, often with pre-existing and underdiagnosed neuropathy, were more frequently and more severely affected. According to medical records, where diagnostics were primarily based on patients' subjective information, even moderate cases were frequently underdiagnosed. A moderate correlation was observed between the increase in NfL and changes in TNSr (r = 0.385, p = 0.004). Patients with cancer affecting the central nervous system (CNS) showed elevated baseline NFL levels. In contrast to non-responders, NFL decreased in patients who responded well to therapy. In conclusion, data underline the necessity of improved diagnostic accuracy of CIPN and support the potential of NFL as a biomarker for its detection. Further investigations should assess its potential in daily oncological routine.Trial registration number: EA2/167/21 (date of registration: 12.08.2021).

Journal of NeurologyVol. 272(11)
Humboldt-Universität zu Berlin (DE), Sana Klinikum Lichtenberg (DE), Bundeswehrkrankenhaus (DE), Fraunhofer Project Centre Wolfsburg (DE), Bundeswehrkrankenhaus Ulm (DE)
Openalex Percentile: Top 60%
Cancer Treatment and Pharmacology
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