Key result
Baseline-tailored hs-TnT screening identifies ICI-induced myocarditis with ~100% sensitivity.
Why the study?
Immune checkpoint inhibitor-induced myocarditis has a 40-50 % mortality rate and is mostly not diagnosed until clinical symptoms emerge.
Does routine monitoring of high-sensitivity troponin-T during immune checkpoint inhibitor therapy allow for early detection of ICI-induced myocarditis in skin cancer patients?
Cohort (n=280)
No
Does routine monitoring of high-sensitivity troponin-T during immune checkpoint inhibitor therapy allow for early detection of ICI-induced myocarditis in skin cancer patients?
Routine screening with high-sensitivity troponin-T, utilizing baseline-specific thresholds, is highly sensitive for early detection of potentially fatal immune checkpoint inhibitor-induced myocarditis.
BACKGROUND: Immune checkpoint inhibitor (ICI)-induced Myocarditis (irMyocarditis) is a rare adverse event with a high mortality rate of 40-50 % and which is mostly not diagnosed until clinical symptoms emerge. OBJECTIVES: This study aims to screen patients for irMyocarditis using high-sensitivity cardiac troponin-T (hs-TnT) before and regularly during therapy with ICI. METHODS: A cohort of 280 cancer patients were prospectively screened for levels of hs-TnT at baseline and prior to every ICI infusion. In case of elevation of hs-TnT, patients were referred for further work-up. RESULTS: In total, 196 patients exhibited a baseline hs-TnT ≤ 14 ng/l (99th percentile concentration for general population; group A) and 84 patients a hs-TnT > 14 ng/l at baseline (group B). An increase of hs-TnT during ICI-treatment was observed in 56 out of 196 (27.6 %) and 56 out of 84 patients (66.7 %) in group A and B. Cardiovascular assessment was performed in 11.2 % and 27.4 % of patients, respectively, and 4.1 % and 9.5 % of patients were diagnosed with irMyocarditis and treated with corticosteroids. No fatalities occurred in any of the 16 irMyocarditis patients. Defining a threshold with the highest sensitivity and maximum specificity in receiver-operating characteristics curves, identified a limit of 22 ng/l (group A) and 60 ng/l (group B) hs-TnT, associated with a sensitivity of 100 % in both and a specificity of 91.0 % and 89.6 %, respectively, to detect irMyocarditis. CONCLUSION: Screening of hs-TnT can identify irMyocarditis early and lead to reduction of MACE and mortality risk through interruption of ICI-treatment and prompt therapy with corticosteroids.
No takes yet. Share an insight, caveat, or question.
Tomsitz et al. (2024) conducted a cohort in Skin cancer receiving immune checkpoint inhibitors (ICI) (n=280). High-sensitivity cardiac troponin-T (hs-TnT) screening was evaluated on Detection of ICI-induced myocarditis (irMyocarditis) using hs-TnT threshold in patients with normal baseline hs-TnT (AUC 0.958 with 100% sensitivity and 91.0% specificity at a 22 ng/l threshold, 95% CI 0.928-0.989). High-sensitivity troponin-T screening accurately predicted ICI-induced myocarditis with 100% sensitivity using thresholds of 22 ng/l for patients with normal baseline and 60 ng/l for those with elevated baseline levels.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: