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Cardiotoxicity associated with immune checkpoint inhibitors: Systematic review and meta-analysis
Lavinia Piazza1, Anna Carollo2, Enrica Di Martino2
1Università degli Studi di Milano, Department of Pharmacy, Italy.
Background And Aims:
The aim of this systematic review was to assess the risk of cardiac toxicity in patients undergoing approved PD-1 (nivolumab, pembrolizumab, cemiplimab, dostarlimab), PD-L1 (atezolizumab, avelumab, durvalumab), and CTLA-4 (ipilimumab) inhibitors.
Results:
Among a total of 2272 articles, 11 phase II and III clinical trials included: 5463 patients and 175 cardiac adverse events. The most common cardiac disorder was atrial fibrillation (12 %), while cardiac arrest and cardiac failure (6 %) led to death in three cases. Overall, ICI treatment increased the risk of cardiotoxicity compared with control groups (RR=1.62, 95 %-CI= 1.18-2.24, p-value=0.0033; OR=1.71, 95 %-CI= 1.20-2.42, p-value=0.0027).
Conclusions:
This study proved that the recognition of frequency and severity of all grade cardiotoxicity associated with ICIs is still underestimated. Thus, a systematic cardiological screening becomes necessary, in order to intercept the potential cardiological complications beforehand and optimize the outcomes of the respective treatment with PD-1, PD-L1 and CTLA-4 inhibitors.
Insights
Immune checkpoint inhibitors (ICIs) like PD-1, PD-L1, and CTLA-4 therapies increase cardiotoxicity risk. Early cardiac screening is vital for managing potential complications and improving patient outcomes during cancer treatment.
Area of Science:
- Oncology
- Cardiology
- Immunotherapy
Background:
- Immune checkpoint inhibitors (ICIs) targeting PD-1, PD-L1, and CTLA-4 are crucial in cancer therapy.
- Cardiac toxicity is a recognized but potentially underestimated adverse effect of these treatments.
Purpose of the Study:
- To systematically review and assess the risk of cardiac toxicity in patients receiving approved PD-1, PD-L1, and CTLA-4 inhibitors.
- To quantify the incidence and types of cardiac adverse events associated with ICI therapy.
Main Methods:
- Systematic review of 2272 articles.
- Inclusion of 11 phase II and III clinical trials.
- Analysis of cardiac adverse events in 5463 patients.
Main Results:
- 175 cardiac adverse events were reported.
- Atrial fibrillation was the most common (12%), followed by cardiac arrest and failure (6%).
- ICI treatment significantly increased cardiotoxicity risk (RR=1.62, OR=1.71).
Conclusions:
- The frequency and severity of ICI-associated cardiotoxicity are underestimated.
- Systematic cardiological screening is necessary to detect and manage potential cardiac complications.
- Proactive cardiac monitoring can optimize treatment outcomes for patients receiving ICIs.
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