IFN-Gamma Expression as a Predictor of Response to Immune Checkpoint Inhibitors in First-Line Metastatic Melanoma

IFN-Gamma Expression in Tumor Tissue and Blood as a Predictor of Response to Immune Checkpoint Inhibitors in the First-Line Treatment of Metastatic Melanoma

This study evaluates whether interferon-gamma (IFN-γ) expression in tumor tissue and peripheral blood can serve as a predictive biomarker of response to immune checkpoint inhibitors in the first-line treatment of metastatic melanoma.

Although immune checkpoint inhibitors have substantially improved outcomes in metastatic melanoma, not all patients respond to therapy. Reliable biomarkers that could help identify patients most likely to benefit from treatment are still lacking.

This study investigates the association between IFN-γ expression levels and objective treatment response. In addition, the study explores whether characteristics of the gut microbiome are associated with immunotherapy outcomes. The results may contribute to improved patient stratification and personalized treatment approaches in metastatic melanoma.

Immune checkpoint inhibitors have significantly improved survival in patients with metastatic melanoma. However, treatment response varies considerably, and a substantial proportion of patients do not achieve durable benefit. The identification of predictive biomarkers remains an important unmet clinical need.

This prospective, single-arm interventional study evaluates biological markers in patients receiving first-line immune checkpoint inhibitor therapy for metastatic melanoma. The primary objective is to assess whether interferon-gamma (IFN-γ) expression in tumor tissue and peripheral blood is associated with objective response to treatment.

Tumor IFN-γ expression is assessed using immunohistochemistry, and peripheral blood IFN-γ concentration is measured using enzyme-linked immunosorbent assay (ELISA). The study also evaluates additional biomarkers, including PD-L1 expression, to explore their potential predictive value.

Furthermore, the study investigates the relationship between gut microbiome composition and treatment outcomes. Microbiome diversity and bacterial taxonomic profiles are analyzed from stool samples to determine whether microbial characteristics are associated with response to immunotherapy.

The study is conducted at a single tertiary oncology center and includes adult patients with metastatic melanoma receiving standard-of-care first-line immune checkpoint inhibitor therapy. The findings aim to support improved risk stratification and biomarker-guided therapeutic decision-making.

Inclusion Criteria:

• Age over 18 years
• Cytologically or histologically verified malignant melanoma
• Stage IIID unresectable/IV according to AJCC classification (8th edition, 2018)
• Performance status WHO 0-2 (ECOG criteria)
• First-line systemic immunotherapy treatment (nivolumab, ipilimumab/nivolumab combination, pembrolizumab)
• CT triple scan/PET CT performed within 4 weeks prior to the first administration
• Signed informed consent for participation in the clinical study

Exclusion Criteria:

• Previous systemic therapy for melanoma
• Performance status WHO 3-4 (ECOG criteria)
• Contraindications for immunotherapy (known immune deficiency, active immunosuppressive treatment, or active autoimmune disease requiring treatment)
• Other malignant diseases (except cured basal cell carcinoma, squamous cell carcinoma, and other cured solid tumors without recurrence more than three years after treatment)