ArticleRespiratory medicine case reports2025
Massive immune-related myositis and cytokine release syndrome during dual immunotherapy plus chemotherapy for recurrent lung adenocarcinoma: case report.
Article in Respiratory medicine case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed, 1 synthesis or guideline pooled it.
- Immune checkpoint inhibitors-related cytokine storm syndrome: a systematic review of characteristics, treatment, and outcomes.Frontiers in immunology · 2026Pooled it
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Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Immune-related myositis (irMyositis) is a rare but potentially life-threatening immune-related adverse event (irAE) associated with immune checkpoint inhibitors (ICIs). We report a case of irMyositis presenting with massive unilateral enlargement of the periarticular hip muscles in a patient with recurrent lung adenocarcinoma after two courses of combination therapy with tremelimumab, durvalumab, and chemotherapy. Computed tomography scans revealed marked unilateral swelling of the gluteal and thigh muscles without evidence of contrast enhancement. Laboratory tests revealed elevated creatine kinase and inflammatory marker levels, and magnetic resonance imaging confirmed muscle inflammation. The patient was diagnosed with irMyositis accompanied by cytokine release syndrome and immune-related pneumonitis. Prompt initiation of high-dose corticosteroids, followed by tocilizumab therapy, has resulted in rapid clinical and radiographic improvements. This case illustrated an uncommon radiological manifestation of irMyositis. It underscores the importance of early recognition and timely immunosuppressive therapy for managing life-threatening irAEs.
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