LAG-3 expression on peripheral blood cells identifies patients with poorer outcomes after immune checkpoint blockade.

Abstract

Immune checkpoint blocking antibodies are a cornerstone in cancer treatment; however, they benefit only a subset of patients and biomarkers to guide immune checkpoint blockade (ICB) treatment choices are lacking. We designed this study to identify blood-based correlates of clinical outcome in ICB-treated patients. We performed immune profiling of 188 ICB-treated patients with melanoma using multiparametric flow cytometry to characterize immune cells in pretreatment peripheral blood. A supervised statistical learning approach was applied to a discovery cohort to classify phenotypes and determine their association with survival and treatment response. We identified three distinct immune phenotypes (immunotypes), defined in part by the presence of a LAG-3⁺CD8⁺ T cell population. Patients with melanoma with a LAG⁺ immunotype had poorer outcomes after ICB with a median survival of 22.2 months compared to 75.8 months for those with the LAG^- immunotype (<i>P</i> = 0.031). An independent cohort of 94 ICB-treated patients with urothelial carcinoma was used for validation where LAG⁺ immunotype was significantly associated with response (<i>P</i> = 0.007), survival (<i>P</i> < 0.001), and progression-free survival (<i>P</i> = 0.004). Multivariate Cox regression and stratified analyses further showed that the LAG⁺ immunotype was an independent marker of outcome when compared to known clinical prognostic markers and previously described markers for the clinical activity of ICB, PD-L1, and tumor mutation burden. The pretreatment peripheral blood LAG⁺ immunotype detects patients who are less likely to benefit from ICB and suggests a strategy for identifying actionable immune targets for further investigation.