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Published on: February 5, 2020
Cardiovascular events after the initiation of immune checkpoint inhibitors
Yuta Suzuki1,2, Hidehiro Kaneko1,3, Yuichi Tamura4
1The Department of Cardiovascular Medicine, The University of Tokyo, Tokyo, Japan.
Abstract:
We sought to clarify the incidence of major adverse cardiac events (MACE) after the initiation of immune checkpoint inhibitors (ICIs). We analyzed the JMDC Claims Database between 2005 and 2021. The study included 2972 patients with no history of cardiovascular disease and a prescription for an ICI. The primary outcome was the incidence of MACE, including myocarditis, pericarditis, Takotsubo cardiomyopathy, atrio-ventricular block, heart failure, myocardial infarction, and stroke. The median age of study participants was 59 (Q1-Q3 53-65) years, and 2163 participants (72.8%) were male. Lung cancer was the most common cancer site (n = 1603). Among ICIs, programmed cell death-1 (PD-1) was most frequently used, and a combination ICI treatment was conducted in 110 patients (3.7%). During a mean follow-up of 358 ± 327 days, 419 MACE events were recorded. The incidence rate of myocarditis, pericarditis, Takotsubo cardiomyopathy, atrio-ventricular block, heart failure, myocardial infarction, and stroke was 3.4, 142.3, 10.3, 17.2, 1191.2, 55.2, and 278.5 per 10,000 person-years, respectively. The incidence of cardiovascular events was higher within 180 days after the initial prescription of ICI. The continuation rate of ICI after MACE was 38.4%. In conclusion, our analysis of a nationwide epidemiological dataset demonstrated the incidence of MACE after the initiation of ICI treatment. The incidence of heart failure was higher than expected, and the continuation rate of ICI treatment after MACE was low. Our results indicated the importance of monitoring and prevention of cardiovascular events in cancer patients requiring ICI treatment.
Insights
Immune checkpoint inhibitors (ICIs) can cause major adverse cardiac events (MACE), including heart failure, particularly within 180 days of treatment initiation. Cardiovascular monitoring is crucial for cancer patients receiving ICIs.
Area of Science:
- Cardiology
- Oncology
- Immunology
Background:
- Immune checkpoint inhibitors (ICIs) are increasingly used in cancer therapy.
- Cardiovascular adverse events are a known but not fully characterized complication of ICI treatment.
- Understanding the incidence of major adverse cardiac events (MACE) is critical for patient safety.
Purpose of the Study:
- To determine the incidence of MACE following the initiation of ICI therapy.
- To identify specific cardiovascular events associated with ICI use.
- To analyze the timing and continuation rates of ICI treatment after MACE.
Main Methods:
- Analysis of the JMDC Claims Database (2005-2021).
- Inclusion of 2972 patients without prior cardiovascular disease receiving ICIs.
- Primary outcome: incidence of MACE (myocarditis, pericarditis, Takotsubo cardiomyopathy, atrio-ventricular block, heart failure, myocardial infarction, stroke).
Main Results:
- The overall incidence rate of MACE was recorded.
- Specific event rates per 10,000 person-years included heart failure (1191.2), stroke (278.5), and myocardial infarction (55.2).
- Cardiovascular events occurred more frequently within 180 days of ICI initiation; ICI continuation post-MACE was 38.4%.
Conclusions:
- ICI treatment is associated with a notable incidence of MACE, with heart failure occurring more frequently than anticipated.
- The timing of MACE suggests a need for vigilant cardiovascular monitoring early in ICI therapy.
- Low ICI continuation rates post-MACE highlight potential treatment modifications and the importance of proactive cardiovascular risk management in oncology patients.
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