Evidence map›Paper›PMID 41152872›Full record

ArticleRespiratory research2025

Modeled reductions in COPD exacerbation rates, mortality, and related medical costs due to increased SITT adoption: PROMETHEUS Italy.

Pierachille Santus, Bianca Oresta, Davide Finocchiaro, Piergiuseppe De Rosa, John Bell, Melissa Caplen, Jennifer Carioto, Prachi Bhatt, Bruce Pyenson, Alberto Papi

Erratum issued 2 registry-linked trialsAbstract read
In one paragraph

Article in Respiratory research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 2 registered trials, which are not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02164513 phase3completednot on this map

A Phase III, 52 Week, Randomized, Double-blind, 3-arm Parallel Group Study, Comparing the Efficacy, Safety and Tolerability of the Fixed Dose Triple Combination FF/UMEC/VI With the Fixed Dose Dual Combinations of FF/VI and UMEC/VI, All Administered Once-daily in the Morning Via a Dry Powder Inhaler in Subjects With Chronic Obstructive Pulmonary Disease

TypeinterventionalSponsorGlaxoSmithKlineRan2014 to 2017Enrolled10,355ConditionsPulmonary Disease, Chronic ObstructiveArmsfluticasone furoate (FF), vilanterol (VI), umeclidinium bromide (UMEC)
NCT02465567 phase3completednot on this map

A Randomized, Double-Blind, Multi-Center, Parallel-Group Study to Assess the Efficacy and Safety of PT010 Relative to PT003 and PT009 on COPD Exacerbations Over a 52-Week Treatment Period in Subjects With Moderate to Very Severe COPD (Ethos)

TypeinterventionalSponsorPearl Therapeutics, Inc.Ran2015 to 2019Enrolled8,588ConditionsCOPDArmsBGF MDI 320/14.4/9.6 μg, GFF MDI 14.4/9.6 μg, BGF MDI 160/14.4/9.6 μg, BFF MDI 320/9.6 μg
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Pierachille SantusDepartment of Biomedical and Clinical Sciences (DIBIC), Division of Respiratory Diseases, Università degli Studi di Milano, Ospedale L. Sacco, ASST Fatebenefratelli- Sacco, Milan, Italy.
Bianca OrestaAstraZeneca, BioPharmaceutical Medical, Milan, Italy.
Davide FinocchiaroBioPharmaceuticals Market Access & Government Affairs, AstraZeneca, Milan, Italy.
Piergiuseppe De RosaAstraZeneca, BioPharmaceutical Medical, Milan, Italy.
John BellAstraZeneca, BioPharmaceutical Medical, Cambridge, United Kingdom.
Melissa CaplenMilliman, New York, USA.
Jennifer CariotoMilliman, New York, USA. Jennifer.Carioto@milliman.com.
Prachi BhattMilliman, New York, USA.
Bruce PyensonMilliman, New York, USA.
Alberto PapiDepartment of Respiratory Medicine, University of Ferrara Medical School, Ferrara, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCOPD is a leading cause of death and significant healthcare burden in Italy. The ETHOS (NCT02465567||5/2015) and IMPACT (NCT02164513||6/2014) randomized controlled trials (RCTs) have evaluated single-inhaler triple therapy (SITT) and have shown SITT efficacy and safety in reducing exacerbations and all-cause mortality in COPD patients. Despite benefits seen in RCTs, there are currently no studies that evaluate the long-term implications of broader and appropriate SITT use in Italy. We therefore evaluated the potential impact of broader SITT adoption on mortality, exacerbations, and related medical costs in Italy.

methodsWe developed a 10-year (2025-2034) microsimulation model using literature-based patient demographic and clinical characteristics, incidence, therapy distribution and changes, COPD severity changes, mortality, and exacerbations to simulate the Italian COPD population. We modeled two scenarios: "status quo" and "increased SITT," and used patients' airflow limitation and exacerbation history (per GOLD guidelines) to choose patients for SITT. The model simulated annual changes in patient characteristics and related changes in medication therapy over 10-years. Patients' progression reflected reductions in % of FEV1 predicted and annual clinical characteristics. Flagged patients were those that qualified for SITT.

resultsA starting population of approximately 1,550,000 diagnosed prevalent and incident COPD patients were included in the analysis. Based on our modeled "increased SITT" simulation and medication transition algorithm, at the end of the 10-year projection, the prevalent and incident COPD population in Italy increased to 1,881,000 patients, of which 45.4% received SITT. Over 10 years, modeled increased SITT treatment reduced severe and moderate Exacerbations by 12% and 13%, respectively, and all-cause mortality by 14%, avoiding 40,000 deaths, compared to status quo treatment for flagged COPD patients. Consequently, higher than current SITT adoption could reduce associated medical costs by €646 million for flagged COPD patients.

conclusionAssuming RCTs effects and adherence translate to clinical practice, our model shows that higher than current SITT use in the Italian COPD population may lead to lower mortality rates and exacerbations, ensuring a substantial savings in associated medical costs. The results of this modeling study could provide rationale to modify existing practices on SITT prescribing with the aim of alleviating the burden of COPD.

Indexed as

Bronchodilator AgentsDisease ProgressionHealth Care CostsNebulizers and VaporizersPulmonary Disease, Chronic ObstructiveAdministration, InhalationAgedFemaleHumansItalyMaleMiddle AgedMortalityBronchodilator AgentsCOPDPopulation modelSingle-inhaler triple therapy

Identifiers

PMID41152872
PMCPMC12570637

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.