# Supportive care: Comparing exercise interventions for upper extremity polyneuropathy induced by chemo- or immunotherapy — VISCIPH B

**Authors:** Stefanie Siebert, Jane Kersten, Sarah Man, Sarina Heinz, Katharina Leuchte, Freerk T. Baumann, Timo Sonntag

PMC · DOI: 10.1007/s00520-026-10459-7 · 2026-03-19

## TL;DR

A pilot study found that a specific exercise program can improve upper limb neuropathy symptoms in cancer patients, showing promise for future research.

## Contribution

The study is the first to investigate supervised exercise interventions for upper-extremity neuropathy in cancer patients.

## Key findings

- Combined sensorimotor and vibration exercise improved patient-reported neuropathy symptoms significantly.
- The exercise intervention was feasible and safe with high adherence and no adverse events.
- Participants in the sensorimotor plus vibration group showed a higher response rate compared to moderate resistance exercise.

## Abstract

Chemotherapy and immunotherapy-induced peripheral neuropathy affects up to 68% of cancer patients and may persist long after treatment, substantially impairing daily functioning and quality of life. While exercise therapy has demonstrated benefits in lower-limb polyneuropathy (PNP), evidence for upper-extremity symptoms remains scarce. The VISCIPH B pilot study investigated the effect of two supervised exercise interventions for PNP of the upper extremities using exploratory analyses of symptom response.

In this single-center randomized controlled pilot trial (DRKS00023287), 61 cancer patients with symptomatic upper-extremity PNP were randomized (1:1) to either (a) combined sensorimotor plus vibration exercise (PNPEX) or (b) moderate resistance exercise (MREX). Both interventions were carried out supervised twice weekly over 12 weeks. Feasibility outcomes included adherence, retention, assessment completeness, and safety of the exercise interventions. Symptom outcomes were assessed with the FACT/GOG-Ntx questionnaire, measures of pain (NRS), depth sensitivity (Rydel-Seiffer tuning fork), and quality of life (EORTC QLQ-C30).

Feasibility criteria showed high adherence (86%) and retention (69%) rates. A total of 42 patients (mean age 53.3 years, 36% male) completed the intervention with no reported intervention-related adverse events. In the exploratory effect analyses, 50% of PNPEX participants (10/20) were classified as responders, compared to 14% (3/21) in MREX (OR = 5.45, p = 0.043). FACT/GOG-Ntx scores improved significantly in PNPEX (p = 0.017) but not in MREX (p = 0.46), resulting in a significant difference between the two groups (p = 0.05). Patient-reported outcomes revealed significant improvements in the PNPEX group regarding numbness and tingling (NRS), depth sensitivity at four of the eight tested bone sites and global health (p = 0.001).

The VISCIPH B pilot trial confirmed the feasibility, safety, and acceptance of supervised exercise for upper-extremity PNP in cancer patients. Significant improvements in patient-reported and functional outcomes indicate that combined sensorimotor and vibration exercise can meaningfully reduce PNP symptoms and should be evaluated in larger trials.

The online version contains supplementary material available at 10.1007/s00520-026-10459-7.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Diseases:** neuropathic symptoms (MESH:D001750), osteolysis (MESH:D010014), numbness (MESH:D006987), diabetes mellitus (MESH:D003920), neuropathic damage (MESH:D009422), Neurotoxic (MESH:D020258), pain (MESH:D010146), chronic alcohol abuse (MESH:D000437), death (MESH:D003643), CIPN (MESH:D010523), bone metastases (MESH:D009362), deterioration (MESH:D000075902), pancreatic, lung, and prostate cancer (MESH:D011471), paresthesia (MESH:D010292), B (MESH:D006509), neuropathic pain (MESH:D009437), multiple myeloma (MESH:D009101), PNP (MESH:D011115), thrombosis (MESH:D013927), motor impairment (MESH:D000068079), COVID-19 (MESH:D000086382), lymphatic malignancies (MESH:D008206), breast cancer (MESH:D001943), symptom (MESH:D012816), Cancer (MESH:D009369), joint (MESH:D007592), or musculoskeletal pain (MESH:D059352)
- **Chemicals:** nivolumab (MESH:D000077594), duloxetine (MESH:D000068736), platinum (MESH:D010984), MREX (-), pembrolizumab (MESH:C582435), taxanes (MESH:D043823), epothilones (MESH:D034261), platinum compounds (MESH:D017671), bortezomib (MESH:D000069286), vinca alkaloids (MESH:D014748)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13002742/full.md

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Source: https://tomesphere.com/paper/PMC13002742