Survival and response to pulmonary vasodilator therapies in patients with chronic obstructive pulmonary disease and pulmonary vascular phenotype.

COPD (chronic obstructive pulmonary disease) Lung transplantation PH (pulmonary hypertension) Simplified risk score

Journal

Respiratory medicine
ISSN: 1532-3064
Titre abrégé: Respir Med
Pays: England
ID NLM: 8908438

Informations de publication

Date de publication:
11 Mar 2024
Historique:
received: 19 10 2023
revised: 13 02 2024
accepted: 03 03 2024
medline: 14 3 2024
pubmed: 14 3 2024
entrez: 13 3 2024
Statut: aheadofprint

Résumé

The aim of the study was to describe and investigate the effect of pulmonary arterial hypertension (PAH) therapies in a cohort of patients with severe precapillary pulmonary hypertension (PH) associated with chronic obstructive pulmonary disease (COPD; PH-COPD), and to assess factors predictive of treatment response and mortality. We retrospectively included patients with severe incident PH-COPD who received PAH therapy and underwent RHC at diagnosis and on treatment. From 2015 to 2022, 35 severe PH-COPD patients, with clinical features of pulmonary vascular phenotype, were included. Seventeen (48.5%) patients were treated with combined PAH therapy. PAH therapy led to a significant improvement in hemodynamics (PVR -3.5 Wood Units (-39.3%); p < 0.0001), and in the simplified four-strata risk-assessment score, which improved by at least one category in 21 (60%) patients. This effect was more pronounced in patients on dual therapy. Kaplan-Meier estimated survival rates at 1, 3 and 5 years were 94%, 65% and 42% respectively. Univariate analysis showed a significant reduction in survival in patients with a higher simplified risk score at follow-up (Hazard ratio (HR) 2.88 [1.16-7.15]; p = 0.02). Hypoxemia <50 mmHg was correlated to mortality in multivariate analysis (HR 4.33 [1.08-17.42]; p = 0.04). Our study confirms the poor prognosis of patients with COPD and a pulmonary vascular phenotype and the potential interest of combined PAH therapy in this population, with good tolerability and greater clinical and hemodynamic improvement than monotherapy. Using the simplified risk score during follow-up could be of interest in this population.

Sections du résumé

BACKGROUND BACKGROUND
The aim of the study was to describe and investigate the effect of pulmonary arterial hypertension (PAH) therapies in a cohort of patients with severe precapillary pulmonary hypertension (PH) associated with chronic obstructive pulmonary disease (COPD; PH-COPD), and to assess factors predictive of treatment response and mortality.
MATERIAL AND METHODS METHODS
We retrospectively included patients with severe incident PH-COPD who received PAH therapy and underwent RHC at diagnosis and on treatment.
RESULTS RESULTS
From 2015 to 2022, 35 severe PH-COPD patients, with clinical features of pulmonary vascular phenotype, were included. Seventeen (48.5%) patients were treated with combined PAH therapy. PAH therapy led to a significant improvement in hemodynamics (PVR -3.5 Wood Units (-39.3%); p < 0.0001), and in the simplified four-strata risk-assessment score, which improved by at least one category in 21 (60%) patients. This effect was more pronounced in patients on dual therapy. Kaplan-Meier estimated survival rates at 1, 3 and 5 years were 94%, 65% and 42% respectively. Univariate analysis showed a significant reduction in survival in patients with a higher simplified risk score at follow-up (Hazard ratio (HR) 2.88 [1.16-7.15]; p = 0.02). Hypoxemia <50 mmHg was correlated to mortality in multivariate analysis (HR 4.33 [1.08-17.42]; p = 0.04).
CONCLUSIONS CONCLUSIONS
Our study confirms the poor prognosis of patients with COPD and a pulmonary vascular phenotype and the potential interest of combined PAH therapy in this population, with good tolerability and greater clinical and hemodynamic improvement than monotherapy. Using the simplified risk score during follow-up could be of interest in this population.

Identifiants

pubmed: 38479707
pii: S0954-6111(24)00059-3
doi: 10.1016/j.rmed.2024.107585
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107585

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Riou reports a relationship with Actelion Pharmaceuticals France SAS that includes: speaking and lecture fees. Riou reports a relationship with MSD France SAS that includes: consulting or advisory, speaking and lecture fees, and travel reimbursement. Riou reports a relationship with Laboratories Menarini France SA that includes: speaking and lecture fees. Riou reports a relationship with Boehringer Ingelheim France SAS that includes: consulting or advisory and travel reimbursement. Canuet reports a relationship with Laboratories Menarini France SA that includes: speaking and lecture fees. Canuet reports a relationship with MSD France SAS that includes: speaking and lecture fees and travel reimbursement. Enache reports a relationship with ChiesiSA France that includes: speaking and lecture fees. Enache reports a relationship with Laboratories Menarini France SA that includes: speaking and lecture fees. Martin reports a relationship with GlaxoSmithKline that includes: speaking and lecture fees. Montani reports a relationship with Acceleron Pharma that includes: consulting or advisory. Montani reports a relationship with MSD France SAS that includes: consulting or advisory and speaking and lecture fees. Montani reports a relationship with Actelion Pharmaceuticals France SAS that includes: consulting or advisory and speaking and lecture fees. Montani reports a relationship with Grupo Ferrer Internacional SA that includes: consulting or advisory. Riou reports a relationship with Grupo Ferrer Internacional SA that includes: consulting or advisory. Montani reports a relationship with Bayer Corporation that includes: speaking and lecture fees. Montani reports a relationship with Boehringer Ingelheim France SAS that includes: speaking and lecture fees. Montani reports a relationship with Chiesi Pharmaceuticals Inc that includes: speaking and lecture fees. Montani reports a relationship with GlaxoSmithKline that includes: speaking and lecture fees. Labani reports a relationship with Boehringer Ingelheim France SAS that includes: speaking and lecture fees. Kessler reports a relationship with GlaxoSmithKline that includes: speaking and lecture fees. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Mathilde Steger (M)

Chest Diseases Department, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.

Matthieu Canuet (M)

Chest Diseases Department, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.

Irina Enache (I)

Department of Physiology and Functional Exploration, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France; University of Strasbourg, Translational Medicine Federation of Strasbourg (FMTS), CRBS, Team 3072 "Mitochondria, Oxidative Stress and Muscle Protection", 1 rue Eugène Boeckel, CS 60026, 67084, Strasbourg, France.

Thibaut Goetsch (T)

Department of Public Health, University Hospital of Strasbourg, Strasbourg, France.

Aissam Labani (A)

Radiology Department, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.

Léo Meyer (L)

Radiology Department, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.

Guillaume Martin (G)

Chest Diseases Department, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France.

Romain Kessler (R)

Chest Diseases Department, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France; INSERM-UNISTRA, UMR 1260 'Regenerative NanoMedicine', University of Strasbourg, 1 rue Eugène Boeckel, CS, 60026, 67084, Strasbourg, France.

David Montani (D)

University of Paris-Saclay, AP-HP, Chest Diseases Department, Hospital of Bicêtre, DMU 5 Thorinno, Inserm UMR_S999, Le Kremlin Bicêtre, France.

Marianne Riou (M)

Chest Diseases Department, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France; Department of Physiology and Functional Exploration, Nouvel Hôpital Civil, University Hospital of Strasbourg, Strasbourg, France; University of Strasbourg, Translational Medicine Federation of Strasbourg (FMTS), CRBS, Team 3072 "Mitochondria, Oxidative Stress and Muscle Protection", 1 rue Eugène Boeckel, CS 60026, 67084, Strasbourg, France. Electronic address: marianne.riou@chru-strasbourg.fr.

Classifications MeSH