# Prognostic Value of Systemic Immune-Inflammation Index in Mucosal Malignant Melanoma

**Authors:** Burak Paçacı, Erkam Kocaaslan, Ahmet Demirel, Fırat Akagündüz, Mustafa Alperen Tunç, Yeşim Ağyol, Ali Kaan Güren, Abdussamed Çelebi, Selver Işık, Ezgi Çoban, Nargiz Majidova, Nadiye Sever, Işık Paçacı, Buket Erkan Özmarasali, Adem Deligönül, Ali Fuat Gürbüz, Melek Karakurt Eryılmaz, Şüheda Ataş İpek, Nisanur Sarıyar Busery, Emre Yılmaz, Murat Sarı, İbrahim Vedat Bayoğlu, Osman Köstek, Nazım Can Demircan

PMC · DOI: 10.3390/jcm15020890 · Journal of Clinical Medicine · 2026-01-22

## TL;DR

This study shows that a blood-based immune marker called SII can predict survival outcomes in patients with mucosal melanoma, a rare and aggressive cancer.

## Contribution

The study is the first to demonstrate the prognostic value of SII in mucosal malignant melanoma.

## Key findings

- High SII was associated with significantly shorter overall survival in MMM patients.
- SII was an independent predictor of worse survival alongside gastrointestinal primary site and metastatic disease.
- SII is a cost-effective and accessible tool for risk stratification in MMM.

## Abstract

Background: Mucosal malignant melanoma (MMM) is a rare and aggressive malignancy with a dismal prognosis. While the Systemic Immune-Inflammation Index (SII) has emerged as a prognostic marker in various solid tumors, its specific value in MMM remains undefined. This study investigated the association between pretreatment SII and overall survival (OS) in patients with MMM. Methods: We retrospectively analyzed 106 adults with histologically confirmed MMM treated at six oncology centers in Turkey between 2005 and 2025. The baseline SII was calculated as platelet × neutrophil/lymphocyte counts obtained before definitive treatment. A receiver operating characteristic (ROC) analysis identified an optimal SII cutoff of 776 for overall survival (OS), defining low (<776) and high (≥776) SII groups. Results: Gastrointestinal and head and neck mucosa were the most frequent primary sites, and one-third of patients presented with metastatic disease. The median OS for the entire cohort was 23.3 months. Patients with a high versus low SII had a shorter OS (16.2 vs. 35.2 months; HR 2.71, 95% CI 1.67–4.40; p < 0.001). In multivariable analysis, a high SII (HR 1.88, 95% CI 1.12–3.14; p = 0.016), gastrointestinal primary site (HR 1.99, 95% CI 1.23–3.23; p = 0.005), and metastatic disease at diagnosis (HR 4.01, 95% CI 2.32–6.94; p < 0.001) independently predicted a worse OS. Conclusions: The SII is a novel, independent prognostic biomarker in MMM. Elevated pretreatment SII correlates with aggressive clinicopathologic features and inferior survival. As a readily accessible and cost-effective marker, SII may facilitate improved risk stratification in routine clinical practice for MMM patients.

## Linked entities

- **Diseases:** metastatic disease (MONDO:0024883)

## Full-text entities

- **Diseases:** MMM (MESH:D008545), malignancy (MESH:D009369), Inflammation (MESH:D007249)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12842355/full.md

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Source: https://tomesphere.com/paper/PMC12842355