ECG and histological findings of the heart in a 63-year-old man with metastatic melanoma who developed fulminant lymphocytic myocarditis following initial.

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Figure 1 (A) Chest computed tomography scans of the patient
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Holter monitor ECG of a 65-year-old man showing marked ST depression of myocardial ischemia when the patient carried out his ordinary work routine as a.
Holter monitor ECG of a 65-year-old man showing marked ST depression of myocardial ischemia when the patient carried out his ordinary work routine as a.
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Recurrence pattern after initial treatment of brain metastases and cause of death. Recurrence pattern after initial treatment of brain metastases and cause.
Meta-analysis of randomised phase III clinical trials with ALK inhibitors in non-small cell lung cancer (NSCLC) showing similar benefit in male patients.
Flow chart of the used methodology adapted from Moher et al
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Mechanism of CTLA-4-induced immunosuppression.
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Prescribers’ responses rating their level of comfort on a scale of 1–5
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Presentation transcript:

ECG and histological findings of the heart in a 63-year-old man with metastatic melanoma who developed fulminant lymphocytic myocarditis following initial doses of nivolumab and ipilimumab and who developed complete heart block.36 Despite intense treatment (intravenous methylprednisolone 1 g/kg daily for 4 days plus infliximab 5 mg/kg), fatal complete heart block occurred. ECG and histological findings of the heart in a 63-year-old man with metastatic melanoma who developed fulminant lymphocytic myocarditis following initial doses of nivolumab and ipilimumab and who developed complete heart block.36 Despite intense treatment (intravenous methylprednisolone 1 g/kg daily for 4 days plus infliximab 5 mg/kg), fatal complete heart block occurred. Initial right bundle branch block (RBBB) and ST depression (A) progressed rapidly to complete heart block and cardiac arrest (B). Autopsy showed lymphocytic infiltration in myocardium (C) comprised CD3+ T cells (D), many of which were CD8+ lymphocytes (E) and CD68+ macrophages (F) (adapted with permission from Johnson et al36). Gilda Varricchi et al. ESMO Open 2017;2:e000247 Copyright © European Society for Medical Oncology. All rights reserved.