Why the study?
Immune checkpoint inhibitors can cause immune-related adverse events, and this study aimed to assess their incidence and management in thymoma patients with preexisting myasthenia gravis receiving ICI therapy.
Does preexisting myasthenia gravis increase the risk of severe immune-related adverse events, including myocarditis, in thymoma patients receiving immune checkpoint inhibitors?
Observational (n=16)
No
Does preexisting myasthenia gravis increase the risk of severe immune-related adverse events, including myocarditis, in thymoma patients receiving immune checkpoint inhibitors?
In patients with thymoma receiving immune checkpoint inhibitors, preexisting myasthenia gravis is associated with a significantly higher risk of severe immune-related adverse events, including life-threatening myocarditis.
May warrant caution with ICIs in thymoma patients with preexisting MG; challenges consensus on routine use in this setting.
Objective Immune checkpoint inhibitors (ICIs) can induce immune system activation and cause immune-related adverse events (irAEs). This study aimed to assess the incidence and management of irAEs in thymoma patients with preexisting MG who received ICI therapy. Methods This was a retrospective observational cohort study. From September 2018 to May 2024, 12,916 patients received ICI therapy at our hospital. Among them, six patients with preexisting MG and thymoma (MGT) received ICI treatment, and ten thymoma patients without MG (TOMA) served as controls. irAEs, MG flares, and treatment outcomes were primarily assessed through retrospective review of medical records. Anti-acetylcholine receptor antibody (AChR-Ab) levels and pathological thymoma tissue features were analyzed to explore the potential mechanisms underlying the irAEs. Results Compared with TOMA patients (n=10), all MGT patients (n=6) had grade 3 or higher irAEs (p=0.034) and experienced ICI-induced myocarditis (p=0.011). All MGT patients experienced symptom exacerbation, including a myasthenic crisis. MGT patients who received immunosuppressive agents before ICI therapy and those who received both steroids and intravenous immunoglobulin (IVIG) during irAE occurrence had better outcomes. AChR-Ab levels markedly increased one month after the onset of irAEs. Furthermore, two TOMA patients with germinal centers (GCs) in their thymus tissues had severe irAEs, whereas two without GCs had no irAEs. Conclusion In this study, irAEs were common and severe in patients with preexisting MG and thymoma following ICI therapy. Pretreatment immunosuppressive therapy was associated with better clinical outcomes. The presence of GCs in thymoma patients without MG may serve as a predictive biomarker for the occurrence of irAEs.
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Sun et al. (2026) conducted an observational in Thymoma with preexisting myasthenia gravis (n=16). Immune checkpoint inhibitors vs. Thymoma patients without myasthenia gravis was evaluated on Grade 3+ immune-related adverse events (irAEs) (null, 95% CI null, p=0.034).
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