The influence of polymorphisms in cytokine genes on pain and response to palliative radiotherapy in multiple myeloma patients: prospective observational study.
Rudzianskiene M, Inciura A, et al. • Scandinavian journal of pain • 2026
Polymorphisms in cytokine genes, specifically IL1RN rs2234677, IL1A rs1800587, IL1B rs1143634, and IL1RN rs315952, significantly influenced pain severity and response to palliative radiotherapy in multiple myeloma patients.
Key Findings
Results
Karnofsky index ≥60% and IL1RN rs2234677 GG genotype were found to have significant impact on severe pain prior to radiation.
81 multiple myeloma patients were enrolled in this prospective observational study.
Pain severity and analgesic dose were evaluated prior to radiotherapy and at 4, 12, and 24 weeks following treatment.
IL1RN rs2234677 is a polymorphism in the IL-1 receptor antagonist encoding gene.
The study analyzed 12 gene polymorphisms across 6 cytokines: IL-6, IL-10, TNFα, IL-1α, IL-1β, and IL-1RA.
Results
Patients with the IL1A rs1800587 CC genotype had significantly better response to palliative radiotherapy.
IL1A rs1800587 is a polymorphism in the IL-1α encoding gene.
Response to radiotherapy was assessed at 4, 12, and 24 weeks post-treatment.
This finding highlights the role of IL-1α gene variation in modulating radiotherapy outcomes for pain in multiple myeloma.
Results
Patients with the IL1B rs1143634 CC genotype had significantly better response to palliative radiotherapy.
IL1B rs1143634 is a polymorphism in the IL-1β encoding gene.
Both IL1A rs1800587 CC and IL1B rs1143634 CC genotypes were independently associated with better radiotherapy response.
These findings emphasize the importance of inflammatory interleukin gene polymorphisms in predicting pain treatment outcomes.
Results
Patients with the IL1RN rs315952 CC genotype had a faster response to palliative radiation.
IL1RN rs315952 is a distinct polymorphism from IL1RN rs2234677, both located in the IL-1 receptor antagonist encoding gene.
The faster response was identified among the time points assessed at 4, 12, and 24 weeks post-radiotherapy.
Two separate IL1RN polymorphisms (rs2234677 and rs315952) were each associated with different aspects of pain and radiotherapy response.
Methods
The study analyzed 12 gene polymorphisms of 6 cytokines involved in pain syndrome pathogenesis in 81 multiple myeloma patients undergoing palliative radiotherapy.
The six cytokines studied were IL-6, IL-10, TNFα, IL-1α, IL-1β, and IL-1RA.
Pain severity and dose of analgesics were evaluated as outcome measures.
Assessments were conducted prior to radiotherapy and at 4, 12, and 24 weeks following treatment.
The study was registered at ClinicalTrials.gov (NCT02024815) and approved by a regional research ethical committee (BE-2-39).
Rudzianskiene M, Inciura A, Gerbutavicius R, Rudzianskas V, Ugenskiene R, Paukstaitiene R, et al.. (2026). The influence of polymorphisms in cytokine genes on pain and response to palliative radiotherapy in multiple myeloma patients: prospective observational study.. Scandinavian journal of pain. https://doi.org/10.1515/sjpain-2025-0013