# Cytokine Dynamics in Bortezomib‐Induced Peripheral Neuropathy: Challenges in Translating Preclinical Findings to Humans

**Authors:** Nadine Cebulla, Daniel Schirmer, Eva Runau, Leon Flamm, Calvin Terhorst, Laura Jähnel, Johanna Güse, Nicola Giordani, Annett Wieser, Felicitas Schoch, Marie‐Luise Reinle, Sonja Gommersbach, Aikaterini Papagianni, Xiang Zhou, Hermann Einsele, Ann‐Kristin Reinhold, Heike Rittner, K. Martin Kortüm, Claudia Sommer

PMC · DOI: 10.1111/jns.70090 · Journal of the Peripheral Nervous System · 2026-01-23

## TL;DR

This study explores cytokine levels in patients with bortezomib-induced peripheral neuropathy, finding limited correlation between cytokines and neuropathy severity.

## Contribution

The study evaluates cytokine dynamics in human patients, revealing discrepancies between preclinical models and clinical observations.

## Key findings

- CCL2 levels were not different among patient groups or compared to healthy controls.
- IL-6 and TNF-α levels were highest in newly treated patients but decreased over time.
- No correlation was found between TNF-α levels and neuropathy severity or daily life impairment.

## Abstract

Bortezomib‐induced peripheral neuropathy (BIPN) remains a common treatment side effect in patients with multiple myeloma (MM). Data from rodent models indicate a role of proinflammatory cytokines in BIPN pathophysiology, making them potential therapeutic targets. We therefore tested cytokine levels throughout the course of BIPN in a cohort of MM patients.

We performed an interim analysis of a monocentric, non‐randomized, observational study including 113 patients with MM. Three groups of patients—within their first cycle of BTZ treatment (FC), with ongoing BTZ treatment at the time of recruiting (OT), and with BTZ treatment in the past (PT)—were compared to controls. Sixteen FC patients were followed up for a median of 6 months. Serum TNF‐α, IL‐6, and CCL2, the cytokines most often implied in the animal models, were analyzed via the ELLA device.

CCL2 levels were not different among our patient groups or in comparison with healthy controls. Compared to healthy controls, the FC group had the highest IL‐6 levels, followed by the PT and then the OT group. The FC group also had higher TNF‐α levels compared to all other groups. Six months after inclusion, patients showed a decrease in TNF‐α levels compared to their baseline. There was no correlation between TNF‐α levels and neuropathy severity or impairment in daily life.

Factors related to MM may influence systemic cytokine levels in BIPN patients, limiting conclusions on their role in BIPN pathophysiology and their utility as drug targets.

## Linked entities

- **Proteins:** TNF (tumor necrosis factor), IL6 (interleukin 6), CCL2 (C-C motif chemokine ligand 2)
- **Chemicals:** bortezomib (PubChem CID 387447)
- **Diseases:** multiple myeloma (MONDO:0009693), peripheral neuropathy (MONDO:0003620)

## Full-text entities

- **Genes:** Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, CASC3 (CASC3 exon junction complex subunit) [NCBI Gene 22794] {aka BTZ, MLN51}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, Tnfrsf1a (TNF receptor superfamily member 1A) [NCBI Gene 25625] {aka TNFR-1, Tnfr1}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, TNFRSF1A (TNF receptor superfamily member 1A) [NCBI Gene 7132] {aka CD120a, FPF, TBP1, TNF-R, TNF-R-I, TNF-R55}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, Mapk8 (mitogen-activated protein kinase 8) [NCBI Gene 116554] {aka JNK}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, Ccl2 (C-C motif chemokine ligand 2) [NCBI Gene 24770] {aka MCP-1, MCP1, Scya2, Sigje}, TNP1 (transition protein 1) [NCBI Gene 7141] {aka TP1}, CD38 (CD38 molecule) [NCBI Gene 952] {aka ADPRC 1, ADPRC1, cADPR1}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** Neuroinflammation (MESH:D000090862), Multiple Myeloma (MESH:D009101), neurological conditions (MESH:D019636), sensory deficits (MESH:D012678), infection (MESH:D007239), plasma cell neoplasm (MESH:D054219), neuropathic (MESH:D009437), Toxicity (MESH:D064420), BIPN (MESH:D010523), axonal damage (MESH:D001480), neurotoxicity (MESH:D020258), axonopathy (MESH:D016472), Neuropathy (MESH:D009422), PN (MESH:C565820), Cancer (MESH:D009369), mechanical allodynia (MESH:D006930), diabetes (MESH:D003920), numbness (MESH:D006987), clinical neuropathy (MESH:D000075902), paresthesias (MESH:D010292), inflammatory (MESH:D007249), Pain (MESH:D010146), pareses (MESH:D010291)
- **Chemicals:** FC (MESH:C095424), daratumumab (MESH:C556306), thalidomide (MESH:D013792), prednisolone (MESH:D011239), Dexamethasone (MESH:D003907), lenalidomide (MESH:D000077269), BTZ (-), Bortezomib (MESH:D000069286), isatuximab (MESH:C000599209), pomalidomide (MESH:C467566)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116], Rodentia (rodent, order) [taxon 9989], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12831098/full.md

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Source: https://tomesphere.com/paper/PMC12831098