PD-1/PD-L1 inhibitors-associated cardiac adverse events : a retrospective and real-world study based on the FDA Adverse Event Reporting System (FAERS)

BACKGROUND: Programmed cell death protein-1 (PD-1) and programmed cell death ligand-1 (PD-L1) inhibitors have reformed the treatment landscape for various malignancies and improved prognosis of patients. However, they also lead to events that although rare may prove to be fatal.

RESEARCH DESIGN AND METHODS: Data from July 2014 to June 2022 based on FDA Adverse Event Reporting System (FAERS) were analyzed. The signal index reporting odds ratio (ROR) was used to evaluate the correlation between cardiac AEs and given medications. The indications and the median time to onset (TTO) of different PD-1/PD-L1 inhibitors were compared.

RESULTS: Cardiac AEs are rare but may be fatal with particular profiles in primary tumor, onset time, and especially gender. We identified 11,538 reports that were related to cardiotoxicity of PD-1/PD-L1 inhibitors, in which 178 different preferred terms (PTs) were distinguished, and nivolumab reported the most PTs with signal. All targeted medications showed signals in myocardial disorders and pericardial disorders, which tend to occur in the first 1-2 months. Non-small cell neoplasm was the top and common indication during anti-PD-1 or anti-PD-L1 therapy with cardiotoxicity.

CONCLUSIONS: This study could help early diagnosis and surveillance of ICIs-related cardiotoxicity.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:23

Enthalten in:

Expert opinion on drug safety - 23(2024), 2 vom: 02. Feb., Seite 257-267

Sprache:

Englisch

Beteiligte Personen:

Wang, Qiaoyun [VerfasserIn]
Xiao, Fengjiao [VerfasserIn]
Zeng, Yanbin [VerfasserIn]
Zhu, Qiaoling [VerfasserIn]
Zhang, Haixia [VerfasserIn]

Links:

Volltext

Themen:

Cardiotoxicity
FAERS database
Immune Checkpoint Inhibitors
Immunotherapy
Journal Article
PD-1
PD-L1
Programmed Cell Death 1 Receptor
Signal mining

Anmerkungen:

Date Completed 14.02.2024

Date Revised 14.02.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1080/14740338.2023.2203483

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM355743477