Frontiers in immunology · 2026
Immune-related adverse events in patients with preexisting myasthenia gravis and thymoma following immune checkpoint inhibitor treatment: a retrospective, observational study.
СтатьяНаблюдательное исследованиеНазвание и аннотация: Перевод в очереди
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Sun Chao, Guo Rongjing, Yin Xunliang, Feng Lanlan, Guo Yize, Xu Yueliang, Hao Sijia, Huang Xiaoxi, Song Na, Gao Ting, Liu Jie, Gong Li, Lu Jiayu, Lu Qiang, Zhou Yongan, Chang Ting
Аннотация
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.
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.