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Poster Display

112P - Close cardiovascular monitoring during the early stages of treatment for patients receiving immune checkpoint inhibitors

Date

07 Dec 2023

Session

Poster Display

Presenters

Danielle Delombaerde

Citation

Annals of Oncology (2023) 20 (suppl_1): 100535-100535. 10.1016/iotech/iotech100535

Authors

D.L. Delombaerde1, N. Van de Veire2, D. Vervloet2, V. Moerman2, L. van Calster2, L. Croes1, F. Gremonprez2, A.M. De Meulenaere2, X. Elzo Kraemer2, K. Wouters3, M. Peeters4, H. Prenen4, J. De Sutter2

Author affiliations

  • 1 AZ Maria Middelares AZMMSJ and Center for Oncological Research (CORE), University of Antwerp, Gent/BE
  • 2 AZ Maria Middelares AZMMSJ, Gent/BE
  • 3 Antwerp University Hospital - Center for Oncological Research (CORE), Edegem/BE
  • 4 UZA - University Hospital Antwerp, Edegem/BE

Resources

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Abstract 112P

Background

Immune checkpoint inhibitors (ICIs) can lead to a wide range of cardiovascular (CV) adverse events. As the population of cancer patients receiving ICIs is rapidly growing, there is a high need for both short- and long- term monitoring tools to promptly detect these side effects. Therefore, we developed a prospective, multicenter trial (NCT05699915) in which we assess different cardiac biomarkers as well as routine three dimensional (3D) echocardiography in cancer patients with a solid tumor treated with ICIs.

Methods

All patients underwent routine investigations of blood parameters (high-sensitivity troponin I and T (hs-TnI and hs-TnT), N-terminal pro-brain natriuretic peptide levels (NT-proBNP), in particular) and a thorough CV follow-up (electrocardiography and echocardiography) at fixed time points. The primary endpoint was defined as the incidence of an elevated hs-TnT above the upper limit of normal (ULN) if the baseline value was normal; or 1.5 ≥ times baseline if the baseline value was above the ULN, during the first three months of treatment. Here, we present the results of a preliminary analysis of the first cohort of 59 patients after three months of follow-up.

Results

The mean patient age was 68 ± 12 years; 76% were men. 56% of the patients received an anti-PD-1 agent, while 19% received anti-PD-L1. Overall, 25% of patients received combination therapy. Troponin elevation, as defined in the primary endpoint, occurred in 10.6% [95% CI: 5.0-22.5]. No patients, however, experienced a clinically significant CV event. Furthermore, there were no changes in 3D left ventricular (LV) ejection fraction or LV global longitudinal strain following three months of ICI treatment (55.95 ± 5.95% vs. 56.05 ± 6.46%, p = 0.903 and -17.8% [-18.5 ; -14.2] vs. -17.0% [-18.8 ; -15.1], p = 0.663). No significant changes in diastolic function or right ventricular function were found either. In addition, there was poor agreement between hs-TnT and hs-TnI.

Conclusions

Our preliminary findings found hs-TnT elevation in 10% of cancer patients during the first three months of ICI therapy. However, no significant changes were noted on 3D echocardiography at three months. Hence, longer follow-up and further research are needed.

Clinical trial identification

NCT05699915.

Legal entity responsible for the study

University of Antwerp.

Funding

Has not received any funding.

Disclosure

C. Vulsteke: Financial Interests, Personal, Advisory Board: MSD, Janssen-Cilag, GSK, Astellas Pharma, BMS, Leo Pharma, Bayer, AstraZeneca, Pfizer, Merck; Financial Interests, Institutional, Research Grant, Funding for research project on immune related toxicities: MSD. N. Van de Veire: Financial Interests, Personal, Advisory Role: Pfizer; Financial Interests, Personal, Speaker’s Bureau: Pfizer, Menarini, Daiichi Sankyo Pharmaceutical; Financial Interests, Personal, Other, Travel, Accomodations, Expenses: Boehringher Ingelheim. D. Vervloet: Financial Interests, Personal, Advisory Role: Novartis, Pfizer, AstraZeneca Co.; Financial Interests, Personal, Speaker’s Bureau: Novartis, Pfizer, Izidok, AstraZeneca Co.; Financial Interests, Personal, Other, Travel, Accomodations, Expenses: Pfizer, Novartis. V. Moerman: Financial Interests, Personal, Other, Honoraria: Menarini; Financial Interests, Personal, Other, Travel, Accomodations, Expenses: Menarini, Daiichi Sankyo Pharmaceutical, Bayer US, LLC. L. van Calster: Financial Interests, Personal, Other, Employment: Maatschap Cardiologie. M. Peeters: Financial Interests, Personal, Advisory Role: Amgen, Bayer, Ipsen, Remedus, Sanofi, Sirtex Medical, Terumo, Merck, MSD, Qurin; Financial Interests, Personal, Leadership Role: Qurin; Financial Interests, Personal, Speaker’s Bureau: Amgen, Bayer US, Llc, Merck Serono, Roche, Sanofi, Servier, Sirtex Medical; Financial Interests, Personal, Stocks or ownership: BIMINI BioTech; Financial Interests, Personal, Other, Honoraria: Amgen, Bayer US, Llc, Sanofi, Servier, Merck, Bristol Myers Squibb, MSD, Roche, Sirtex Medical; Financial Interests, Personal, Funding: Amgen, Bayer US, Llc, Ipsen, Novartis, Roche. H. Prenen: Financial Interests, Institutional, Advisory Board: Amgen, Roche, AstraZeneca; Financial Interests, Institutional, Invited Speaker: Bayer, Ipsen, Sanofi. J. De Sutter: Financial Interests, Personal, Advisory Role: Novartis, Bayer US, Llc. All other authors have declared no conflicts of interest.

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