# Prognostic Significance of the Systemic Inflammation Response Index (SIRI) in Patients with Hodgkin Lymphoma

**Authors:** Kadir Ilkkilic, Bayram Sen

PMC · DOI: 10.3390/medicina62020264 · 2026-01-27

## TL;DR

This study shows that a high SIRI score in Hodgkin lymphoma patients is linked to worse outcomes and can help identify high-risk cases.

## Contribution

The study identifies SIRI as an independent prognostic factor in Hodgkin lymphoma patients.

## Key findings

- High SIRI was associated with advanced disease stage, poor treatment response, and increased mortality.
- High SIRI was an independent prognostic factor for shorter progression-free and overall survival.
- SIRI correlated positively with higher IPS-7 scores.

## Abstract

Background and Objectives: Interest in biomarkers reflecting the inflammatory nature of Hodgkin lymphoma (HL) is increasing. This study aimed to evaluate the prognostic significance of the Systemic Inflammation Response Index (SIRI) in patients with HL. Materials and Methods: In this study, 105 patients diagnosed with classical HL at the Hematology Clinic of Recep Tayyip Erdoğan University Faculty of Medicine between January 2015 and April 2025 were retrospectively evaluated. Patients were divided into 2 groups according to the SIRI cut-off value. Results: A high SIRI (≥3.78) was significantly associated with advanced disease stage, poor performance status, higher IPS-7 and IPS-3 scores, non-response or partial response to treatment, relapse, and increased mortality. A positive correlation was found between SIRI and IPS 7 scores (p < 0.001, rho = 0.355). In the univariate analysis for progression-free survival (PFS), hemoglobin, IPS 7 score, and SIRI were identified as prognostic factors; in the multivariate analysis, high SIRI was identified as an independent prognostic factor (p = 0.033). In the univariate analysis for overall survival (OS), age, hemoglobin, albumin, lymphocyte count, IPS 7 score, and SIRI were identified as prognostic factors; and, in the multivariate analysis, age over 45 and high SIRI were identified as independent prognostic factors (p = 0.016, p = 0.012). In the survival analysis, high SIRI levels were associated with shorter PFS and OS (p = 0.001, p < 0.001). Additionally, PFS and OS durations were shorter in patients with high IPS 7 scores (p < 0.001, p < 0.001). Conclusions: A high SIRI prior to treatment was identified as an independent prognostic factor in HL patients and was associated with shorter PFS and OS. This index may help identify high-risk patients and assist clinicians in their decision-making processes by enabling individualized risk assessment.

## Linked entities

- **Diseases:** Hodgkin lymphoma (MONDO:0004952)

## Full-text entities

- **Genes:** CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, ISYNA1 (inositol-3-phosphate synthase 1) [NCBI Gene 51477] {aka INO1, INOS, IPS, IPS 1, IPS-1}
- **Diseases:** gastric cancer (MESH:D013274), lung adenocarcinoma (MESH:D000077192), HL (MESH:D006689), autoinflammatory diseases (MESH:D056660), injury to (MESH:D014947), Inflammation (MESH:D007249), pancreatic cancer (MESH:D010190), peripheral T-cell lymphoma (MESH:D016411), Tumor (MESH:D009369), central nervous system lymphoma (MESH:D008223), breast cancer (MESH:D001943), non-Hodgkin lymphoma (MESH:D008228), Systemic (MESH:D015619), diffuse large B-cell lymphoma of (MESH:D016403), tract (MESH:D014570), renal cell carcinoma (MESH:D002292), T-cell lymphoma (MESH:D016399), metastasis (MESH:D009362), death (MESH:D003643), infections (MESH:D007239), stage IV disease (MESH:D007676), nodal (MESH:D013611), gastric lymphoma (MESH:D018442), toxicity (MESH:D064420)
- **Chemicals:** ABVD (MESH:C034632), bleomycin (MESH:D001761), dacarbazine (MESH:D003606), vinblastine (MESH:D014747), bilirubin (MESH:D001663), brentuximab vedotin (MESH:D000079963), steroid (MESH:D013256), doxorubicin (MESH:D004317)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941707/full.md

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Source: https://tomesphere.com/paper/PMC12941707