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Purpose To evaluate the pan-immune-inflammation value (PIV) and systemic immune-inflammation index (SII) in patients with cutaneous melanoma (CM) under immune checkpoint inhibitor (ICI) therapy. Methods PIV and SII were calculated before the start of ICI therapy and at time of progression/death in patients with metastatic CM (stage III/IV). Sex–age-matched CM patients in stage I/II and healthy subjects (HC) served as controls. Results The median PIV of stage III/IV patients was significantly ( P  = 0.0011) higher than in stage I/II patients and HC. SII was significantly ( P  = 0.00044) lower in HC than in CM patients. At baseline, PIV and SII did significantly correlate with lactate dehydrogenase ( P  = 0.045/0.017). However, ROC curve statistics revealed that SII and PIV were not significantly associated with clinical parameters, including best response to ICI treatment ( P  = 0.87/0.64), progression-free survival ( P  = 0.73/0.91), and melanoma-specific survival ( P  = 0.13/0.17). Moreover, there were no significant changes of PIV and SII from baseline to progression/death ( P  = 0.38/0.52). Conclusions Even though both immune-inflammation biomarkers showed some power to differentiate between CM stages and HC, respectively, PIV and SII seem not to be significant predictors for clinical outcome measures of CM patients under ICI therapy.

The pan-immune-inflammation value and systemic immune-inflammation index in advanced melanoma patients under immunotherapy