Adverse effects of immune checkpoint inhibitor therapies on right ventricular function and pulmonary arterial dilatation

Immunologic risk factors contribute to endothelial dysfunction and development of pulmonary vascular disease. Immune checkpoint inhibitors, used as immunotherapies for malignancies, have a wide range of reported immune-related adverse events. We retrospectively describe the impact of immune checkpoi...

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Main Authors: Ruben Mylvaganam, Ryan Avery, Isaac Goldberg, Courtney Makowski, Ravi Kalhan, Victoria Villaflor, Michael J. Cuttica
Format: Article
Language:English
Published: SAGE Publishing 2021-02-01
Series:Pulmonary Circulation
Online Access:https://doi.org/10.1177/2045894021992236
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spelling doaj-5e099bbc22a64e25ab142d4c6750e6ed2021-02-10T17:33:35ZengSAGE PublishingPulmonary Circulation2045-89402021-02-011110.1177/2045894021992236Adverse effects of immune checkpoint inhibitor therapies on right ventricular function and pulmonary arterial dilatationRuben MylvaganamRyan AveryIsaac GoldbergCourtney MakowskiRavi KalhanVictoria VillaflorMichael J. CutticaImmunologic risk factors contribute to endothelial dysfunction and development of pulmonary vascular disease. Immune checkpoint inhibitors, used as immunotherapies for malignancies, have a wide range of reported immune-related adverse events. We retrospectively describe the impact of immune checkpoint inhibitors on the development of pulmonary vascular injury and right ventricular dysfunction as compared across both computed tomography and transthoracic echocardiography. Twenty-four of 389 patients treated with immune checkpoint inhibitors at a single academic center between 2015 and 2019 were evaluated. Thirteen (54%) patients were treated with anti-programmed cell death receptor 1 (PD-1), 8 (33%) with anti-programmed death receptor ligand 1 (PD-L1) therapy, and 3 (13%) with combination anti-PD-1 and anti-cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) therapy. At a median of 85 days of immune checkpoint inhibitor therapy, RVfwLS significantly increased from –20.6% to –16.7% ( p  = 0.002). After a median of 59 days of immune checkpoint inhibitor therapy, median pulmonary artery to aorta ratio worsened from 0.83 to 0.89 ( p  = 0.03). There was an correlation of duration of immune checkpoint inhibitor therapy (β = –0.574, p  = 0.003) with percent change in RVfwLS. Patients who received anti-PD-1 therapy (β = –0.796, p  = 0.001) showed the greatest correlation of duration of immune checkpoint inhibitor therapy with percent change in RVfwLS. Exposure to immune checkpoint inhibitors are associated with RV dysfunction and vascular changes as measured by strain and computed tomography, respectively.https://doi.org/10.1177/2045894021992236
collection DOAJ
language English
format Article
sources DOAJ
author Ruben Mylvaganam
Ryan Avery
Isaac Goldberg
Courtney Makowski
Ravi Kalhan
Victoria Villaflor
Michael J. Cuttica
spellingShingle Ruben Mylvaganam
Ryan Avery
Isaac Goldberg
Courtney Makowski
Ravi Kalhan
Victoria Villaflor
Michael J. Cuttica
Adverse effects of immune checkpoint inhibitor therapies on right ventricular function and pulmonary arterial dilatation
Pulmonary Circulation
author_facet Ruben Mylvaganam
Ryan Avery
Isaac Goldberg
Courtney Makowski
Ravi Kalhan
Victoria Villaflor
Michael J. Cuttica
author_sort Ruben Mylvaganam
title Adverse effects of immune checkpoint inhibitor therapies on right ventricular function and pulmonary arterial dilatation
title_short Adverse effects of immune checkpoint inhibitor therapies on right ventricular function and pulmonary arterial dilatation
title_full Adverse effects of immune checkpoint inhibitor therapies on right ventricular function and pulmonary arterial dilatation
title_fullStr Adverse effects of immune checkpoint inhibitor therapies on right ventricular function and pulmonary arterial dilatation
title_full_unstemmed Adverse effects of immune checkpoint inhibitor therapies on right ventricular function and pulmonary arterial dilatation
title_sort adverse effects of immune checkpoint inhibitor therapies on right ventricular function and pulmonary arterial dilatation
publisher SAGE Publishing
series Pulmonary Circulation
issn 2045-8940
publishDate 2021-02-01
description Immunologic risk factors contribute to endothelial dysfunction and development of pulmonary vascular disease. Immune checkpoint inhibitors, used as immunotherapies for malignancies, have a wide range of reported immune-related adverse events. We retrospectively describe the impact of immune checkpoint inhibitors on the development of pulmonary vascular injury and right ventricular dysfunction as compared across both computed tomography and transthoracic echocardiography. Twenty-four of 389 patients treated with immune checkpoint inhibitors at a single academic center between 2015 and 2019 were evaluated. Thirteen (54%) patients were treated with anti-programmed cell death receptor 1 (PD-1), 8 (33%) with anti-programmed death receptor ligand 1 (PD-L1) therapy, and 3 (13%) with combination anti-PD-1 and anti-cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) therapy. At a median of 85 days of immune checkpoint inhibitor therapy, RVfwLS significantly increased from –20.6% to –16.7% ( p  = 0.002). After a median of 59 days of immune checkpoint inhibitor therapy, median pulmonary artery to aorta ratio worsened from 0.83 to 0.89 ( p  = 0.03). There was an correlation of duration of immune checkpoint inhibitor therapy (β = –0.574, p  = 0.003) with percent change in RVfwLS. Patients who received anti-PD-1 therapy (β = –0.796, p  = 0.001) showed the greatest correlation of duration of immune checkpoint inhibitor therapy with percent change in RVfwLS. Exposure to immune checkpoint inhibitors are associated with RV dysfunction and vascular changes as measured by strain and computed tomography, respectively.
url https://doi.org/10.1177/2045894021992236
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