About this trial
Cutaneous melanoma is an aggressive malignancy with a rising global incidence; its prognosis has been radically transformed by immune checkpoint inhibitors (ICIs), a class of immunotherapeutic agents targeting immune regulatory pathways such as programmed cell death protein 1 (PD-1), cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), and lymphocyte activation gene 3 (LAG-3). Currently approved first-line treatment strategies-including anti-PD-1 monotherapy and the combinations of nivolumab plus ipilimumab and nivolumab plus relatlimab-have demonstrated significant survival benefits, although combination regimens are associated with a considerably more burdensome toxicity profile compared with monotherapy. Despite these major therapeutic advances, the optimal treatment choice for each individual patient remains uncertain, primarily due to the lack of validated predictive biomarkers in the metastatic setting. This unmet clinical need represents the central rationale of the present study, which aims to bridge this gap through the systematic collection and integrated analysis of clinical, pathological, and molecular data from approximately 200 patients treated with first-line immunotherapy at the European Institute of Oncology.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients with a diagnosis of metastatic or locally advanced unresectable melanoma
Patients treated with first-line immunotherapy as monotherapy (e.g., pembrolizumab or nivolumab) or in combination (e.g., ipilimumab - nivolumab or nivolumab - relatlimab)
Patients treated at IEO (Milan) from 01/01/2022 to 30/11/2027
Age ≥18 years
Disqualifiers
Patients who received targeted therapy as first-line treatment for metastatic melanoma
Patients with a diagnosis of resectable stage III melanoma or operated stage IV with no evidence of disease (NED)
Trial population
The study will include patients who received an immune checkpoint inhibitors agent for their metastatic melanoma from 01/01/2022 until 30/11/2027 at IEO, Milan.
Trial design
Other
Other
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Progression-Free Survival Rate
The progression-free survival (PFS) rate will be evaluated to identify clinical and/or biological predictive markers of efficacy of first-line immune checkpoint inhibitor (ICI) therapy in patients with metastatic melanoma treated at the European Institute of Oncology (IEO), receiving either ICI monotherapy (pembrolizumab or nivolumab) or ICI combination therapy (nivolumab plus ipilimumab or nivolumab plus relatlimab).
Secondary outcomes
Real-world Overall Survival
Real-world Overall Survival
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: