» Articles » PMID: 34229760

Prognostic Impact of Immune-related Adverse Events on Patients with and Without Cardiovascular Disease: a Retrospective Review

Abstract

Background: The emergence of immune checkpoint inhibitors (ICIs) has brought about a paradigm shift in cancer treatment as the use of these drugs has become more frequent and for a longer duration. As a result of T-cell-mediated inflammation at the programmed cell death-1, programmed death-ligand-1, and cytotoxic T-lymphocyte antigen-4 pathways, immune-related adverse events (irAEs) occur in various organs and can cause a rare but potentially induced cardiotoxicity. Although irAEs are associated with the efficacy of ICI therapy and better prognosis, there is limited information about the correlation between irAEs and cardiotoxicity and whether the benefits of irAEs apply to patients with underlying cardiovascular disease. This study aimed to investigate the association of irAEs and treatment efficacy in patients undergoing ICI therapy with and without a cardiovascular history.

Methods: We performed a retrospective review of the medical records of 409 consecutive patients who received ICI therapy from September 2014 to October 2019.

Results: Median patient age was 69 years (29.6% were female). The median follow-up period was 278 days. In total, 69 (16.9%) patients had a history of any cardiovascular disease and 14 (3.4%) patients experienced cardiovascular irAEs after ICI administration. The rate of cardiovascular irAEs was higher in patients with prior non-cardiovascular irAEs than without. The prognosis of patients with irAEs ( +) was significantly better than that of the patients without irAEs (P < 0.001); additionally, this tendency did not depend on the presence or absence of a cardiovascular history. Furthermore, the Cox proportional hazards analysis revealed that irAEs were an independent predictor of mortality.

Conclusions: Although cardiovascular irAEs may be related to prior non-cardiovascular irAEs under ICI therapy, the occurrence of irAEs had a better prognostic impact and this tendency was not affected by cardiovascular history.

Citing Articles

Clinical characteristics and influencing factors of anti-PD-1/PD-L1-related severe cardiac adverse event: based on FAERS and TCGA databases.

Cheng X, Lin J, Wang B, Huang S, Liu M, Yang J Sci Rep. 2024; 14(1):22199.

PMID: 39333574 PMC: 11436968. DOI: 10.1038/s41598-024-72864-4.


Cardiotoxicity induced by immune checkpoint inhibitor: The complete insight into mechanisms, monitoring, diagnosis, and treatment.

Ganesh S, Zhong P, Zhou X Front Cardiovasc Med. 2022; 9:997660.

PMID: 36204564 PMC: 9530557. DOI: 10.3389/fcvm.2022.997660.


Risk Factors and Biomarkers for Immune-Related Adverse Events: A Practical Guide to Identifying High-Risk Patients and Rechallenging Immune Checkpoint Inhibitors.

Chennamadhavuni A, Abushahin L, Jin N, Presley C, Manne A Front Immunol. 2022; 13:779691.

PMID: 35558065 PMC: 9086893. DOI: 10.3389/fimmu.2022.779691.

References
1.
Mahmood S, Fradley M, Cohen J, Nohria A, Reynolds K, Heinzerling L . Myocarditis in Patients Treated With Immune Checkpoint Inhibitors. J Am Coll Cardiol. 2018; 71(16):1755-1764. PMC: 6196725. DOI: 10.1016/j.jacc.2018.02.037. View

2.
Comont T, Sibaud V, Mourey L, Cougoul P, Beyne-Rauzy O . Immune checkpoint inhibitor-related acral vasculitis. J Immunother Cancer. 2018; 6(1):120. PMC: 6240222. DOI: 10.1186/s40425-018-0443-6. View

3.
Heinzerling L, Ott P, Hodi F, Husain A, Tajmir-Riahi A, Tawbi H . Cardiotoxicity associated with CTLA4 and PD1 blocking immunotherapy. J Immunother Cancer. 2016; 4:50. PMC: 4986340. DOI: 10.1186/s40425-016-0152-y. View

4.
Matsuoka H, Hayashi T, Takigami K, Imaizumi K, Shiroki R, Ohmiya N . Correlation between immune-related adverse events and prognosis in patients with various cancers treated with anti PD-1 antibody. BMC Cancer. 2020; 20(1):656. PMC: 7362440. DOI: 10.1186/s12885-020-07142-3. View

5.
Johnson D, Balko J, Compton M, Chalkias S, Gorham J, Xu Y . Fulminant Myocarditis with Combination Immune Checkpoint Blockade. N Engl J Med. 2016; 375(18):1749-1755. PMC: 5247797. DOI: 10.1056/NEJMoa1609214. View