Abstract 2183P
Background
High quality evidence on the incidence of Immune checkpoint inhibitor (ICI) induced-myocarditis and its relationship with LV systolic function is lacking. Anecdotally, a relationship between ICI myocarditis with clinical heart failure in the context of a preserved ejection fraction (HFpEF) was noted and has been investigated here.
Methods
A retrospective analysis of 65 patients with ICI myocarditis was conducted over a 55 month period at the Clatterbridge Cancer Centre, Liverpool UK. A diagnosis of myocarditis was confirmed by cMRI or the cardio-oncology team. Diuresis at any point following myocarditis diagnosis, cMRI findings and peak pro-BNP (BNP) was recorded. Statistical analysis was undertaken with an unpaired t test.
Results
The incidence of ICI myocarditis across all ICI treated patients was 1.74% (n=65/3728); cMRI confirmed (n=53), clinical diagnosis in the absence of cMRI confirmation (n=5) or cMRI clinically unfeasible (n=7).The mean and median EF for all imaged patients (n=58) was 63.07% vs 64%. 82.76% (n=48/58) had a normal / above normal EF. LV impairment was found in 17.24% of patients (n=10/58); 8 mild LVSD, 1 moderate LVSD and 1 severe LVSD. Of all imaged patients 50% (n=29/58) required diuresis. The difference between the mean EF for patients requiring diuresis (EF 61.07%) vs non-diuresed patients (65.14%) was insignificant (p=0.21). 36.21% (n=21/58) of the imaged cohort had HFpEF. The mean peak BNP of diuresed patients was significantly higher (p<0.01) than the non-diuresed cohort (11287 vs 6083). The median peak BNP was also higher in the diuresed cohort (7552 vs 2577).
Conclusions
In this cohort ICI myocarditis was characterised generally by a preserved ejection fraction, however 50% of patients illustrated fluid overload and a third displayed HFpEF therefore the absence of LVSD does not exclude ICI myocarditis. Patients presenting with fluid overload and/or elevated pro-BNPs is a common clinical presentation of ICI myocarditis even in the presence of a maintained EF. Patients should be optimised with diuretics alongside immunosuppression in this setting and cMRI should be performed to confirm the diagnosis as ECHO alone is insufficient to do so.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
R. Dobson: Financial Interests, Personal, Other, Personal honoraria: BMS, Roche. A.C. Olsson-Brown: Financial Interests, Personal, Invited Speaker: BMS, MSD, Eisai, Novartis, Bo-In, Roche, AstraZeneca; Financial Interests, Personal, Research Grant: UCB Pharma, Roche, Eli Lilly, Novartis; Financial Interests, Personal, Other, Travel: Ipsen; Financial Interests, Personal, Other, Educational grant: BMS. All other authors have declared no conflicts of interest.
Resources from the same session
2204P - Clinical predictors and inflammatory markers for malignant pleural mesothelioma prognosis: A retrospective study in a Spanish Medical Oncology Unit
Presenter: Mora Guardamagna
Session: Poster session 07
2205P - Tumor-infiltrating lymphocytes score possesses a relation with adjuvant chemo-immunotherapy benefit and cellular morphology in large-cell neuroendocrine carcinoma
Presenter: Zhiwen Luo
Session: Poster session 07
2207P - Mainstream germline genetic testing in routine oncological care of EGFR mutant non-small cell lung cancer in the United Kingdom
Presenter: Hazel O'Sullivan
Session: Poster session 07
2208P - The single-cell proteomic landscape of pulmonary lymphoepithelioma-like carcinoma
Presenter: Chi Cho
Session: Poster session 07
2209P - Mutational status of non-small cell lung cancer in Portugal: A multicentric study
Presenter: Joana Duarte
Session: Poster session 07
2210P - Reprogramming of pyrimidine metabolism drives tumorigenesis in NF2-deficient malignant pleural mesothelioma
Presenter: Duo Xu
Session: Poster session 07
2234P - Local immune-related adverse events (irAEs) are more common in tumor-bearing organs
Presenter: Steve Blum
Session: Poster session 07
2235P - Chemotherapy priming leads to hypermutability and immune surveillance in colorectal cancer
Presenter: Pietro Paolo Vitiello
Session: Poster session 07
2236P - MHC-II neoantigens and copy number alterations (CNA) drive immune checkpoint inhibitor (ICI) response in metastatic melanoma (MM)
Presenter: Benjamin Shum
Session: Poster session 07