Abstract:I mmune checkpoint inhibitor (ICI)-induced myocarditis (ICI-M) is one of the most serious immunotherapy-related toxicities (1)(2)(3)(4). By reactivating the immune response against a tumor, ICIs can lead to numerous immune-related adverse events, including ICI-M. Although this cardiovascular event is uncommon, the case fatality rate is high, at approximately 30%-50%, and early administration of corticosteroids is required to improve the prognosis (5-7). We need better knowledge of the features of this emerging… Show more
“…The lower rate of LGE and the lower sensitivity of the 2018-LL criteria in ICI-M than in viral myocarditis was confirmed in a recent study. 8 Several hypotheses may explain these results, including lack of standardization of CMR protocols and ICI-M definition, small sample size of biopsy-proven cases, and the early initiation of corticosteroid therapy, which may have affected the diagnostic performance of CMR. 7 Finally, CMR results may be influenced by the patient characteristics.…”
Section: What Are the Unique Features Of Ici-induced Myocarditis?mentioning
“…The lower rate of LGE and the lower sensitivity of the 2018-LL criteria in ICI-M than in viral myocarditis was confirmed in a recent study. 8 Several hypotheses may explain these results, including lack of standardization of CMR protocols and ICI-M definition, small sample size of biopsy-proven cases, and the early initiation of corticosteroid therapy, which may have affected the diagnostic performance of CMR. 7 Finally, CMR results may be influenced by the patient characteristics.…”
Section: What Are the Unique Features Of Ici-induced Myocarditis?mentioning
“…Cardiac magnetic resonance (CMR) has evolved as an standard noninvasive tool for the diagnosis and evaluation of myocarditis. Late gadolinium enhancement (LGE) is associated with a poor prognosis in patients with ICI-induced myocarditis ( 12 ). Myocardial biopsy and CMR are often not available in the setting of an acute presentation.…”
Immune checkpoint inhibitors (ICI) have improved clinical outcomes of patients with advanced lung cancer, but may lead to fatal cardiac injury. We describe a 66-year-old man with advanced lung adenocarcinoma who presented with chest pain and dyspnea 3 weeks after the first dose of sintilimab. The initial electrocardiogram (ECG) demonstrated ST-elevation in leads V5-V9, and a high-sensitivity troponin level was significantly elevated. However, coronary angiography did not reveal any significant stenosis. The patient was successfully treated with methylprednisolone and immunoglobulin. Cardiac MRI was carried out before discharge and late gadolinium enhancement (LGE) was found to be in the mid layer of the septal segment and the subepicardial layer of the inferolateral wall. Due to the high fatality, ICI-related myocarditis requires close surveillance, prompt management and long-term follow-up.
“…In a recent study, although the global LGE was less frequent in patients with ICI-myocarditis than those with viral myocarditis, septal and midwall layer LGE was more common. Septal LGE was the only CMR predictor of MACE at 1 year after adjustment for peak troponin (84).…”
The development of various antitumor drugs has significantly improved the survival of patients with cancer. Many first-line chemotherapy drugs are cytotoxic and the cardiotoxicity is one of the most significant effects that could leads to poor prognosis and decreased survival rate. Cancer treatment include traditional anthracycline drugs, as well as some new targeted drugs such as trastuzumab and ICIs. These drugs may directly or indirectly cause cardiovascular injury through different mechanisms, and lead to increasing the risk of cardiovascular disease or accelerating the development of cardiovascular disease. Cardiotoxicity is clinically manifested by arrhythmia, decreased cardiac function, or even sudden death. The cardiotoxicity caused by traditional chemotherapy drugs such as anthracyclines are significantly known. The cardiotoxicity of some new antitumor drugs such like immune checkpoint inhibitors (ICIs) is also relatively clear and requiring further observation and verification. This review is focused on major three drugs with relatively high incidence of cardiotoxicity and poor prognosis and intended to provide an update on the clinical complications and outcomes of these drugs, and we innovatively summarize the monitoring status of survivors using these drugs and discuss the biomarkers and non-invasive imaging features to identify early cardiotoxicity. Finally, we summarize the prevention that decreasing antitumor drugs-induced cardiotoxicity.
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