Evidence map›Paper›PMID 37979971›Full record

ArticleThorax2024

Survival analysis from the INCREASE study in PH-ILD: evaluating the impact of treatment crossover on overall mortality.

Steven D Nathan, Shilpa Johri, Joanna M Joly, Christopher S King, Amresh Raina, Colleen A McEvoy, Dasom Lee, Eric Shen, Peter Smith, Chunqin Deng and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Thorax, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 4% of its field
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

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  13. Pulmonary hypertension associated with lung diseases.The European respiratory journal · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 7 institutions in 1 country.

Steven D NathanAdvanced Lung Disease and Lung Transplant Program, Inova Heart and Vascular Institute, Inova Fairfax Hospital, Falls Church, Virginia, USA steven.nathan@inova.org.ORCID 0000-0002-6270-1617
Shilpa JohriPulmonary and Critical Care Medicine, Pulmonary Associates of Richmond Inc, Richmond, Virginia, USA.
Joanna M JolyDivision of Cardiovascular Disease, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Christopher S KingAdvanced Lung Disease and Lung Transplant Program, Inova Heart and Vascular Institute, Inova Fairfax Hospital, Falls Church, Virginia, USA.
Amresh RainaAdvanced Heart Failure and Transplant, Allegheny General Hospital, Pittsburgh, Pennsylvania, USA.
Colleen A McEvoyDivision of Pulmonary and Critical Care Medicine, Washington University in St Louis, St Louis, Missouri, USA.
Dasom LeeUnited Therapeutics, Research Triangle Park, North Carolina, USA.
Eric ShenUnited Therapeutics, Research Triangle Park, North Carolina, USA.
Peter SmithUnited Therapeutics, Research Triangle Park, North Carolina, USA.
Chunqin DengUnited Therapeutics, Research Triangle Park, North Carolina, USA.
Aaron B WaxmanPulmonary Vascular Disease Program, Brigham and Women's Hospital/Harvard Medical School, Boston, Massachusetts, USA.
Triangle · USInova Fairfax Hospital · USAllegheny General Hospital · USBrigham and Women's Hospital · USPulmonary Associates · USUniversity of Alabama at Birmingham · USWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveA post-hoc analysis of the INCREASE trial and its open-label extension (OLE) was performed to evaluate whether inhaled treprostinil has a long-term survival benefit in patients with pulmonary hypertension associated with interstitial lung disease (PH-ILD).

methodsTwo different models of survival were employed; the inverse probability of censoring weighting (IPCW) and the rank-preserving structural failure time (RPSFT) models both allow construction of a pseudo-placebo group, thereby allowing for long-term survival evaluation of patients with PH-ILD receiving inhaled treprostinil. Time-varying stabilised weights were calculated by fitting Cox proportional hazards models based on the baseline and time-varying prognostic factors to generate weighted Cox regression models with associated adjusted HRs.

resultsIn the INCREASE trial, there were 10 and 12 deaths in the inhaled treprostinil and placebo arms, respectively, during the 16-week randomised trial. During the OLE, all patients received inhaled treprostinil and there were 29 and 33 deaths in the prior inhaled treprostinil arm and prior placebo arm, respectively. With a conventional analysis, the HR for death was 0.71 (95% CI 0.46 to 1.10; p=0.1227). Both models demonstrated significant reductions in death associated with inhaled treprostinil treatment with HRs of 0.62 (95% CI 0.39 to 0.99; p=0.0483) and 0.26 (95% CI 0.07 to 0.98; p=0.0473) for the IPCW and RPSFT methods, respectively.

conclusionTwo independent modelling techniques that have been employed in the oncology literature both suggest a long-term survival benefit associated with inhaled treprostinil treatment in patients with PH-ILD.

Indexed as

Hypertension, PulmonaryLung Diseases, InterstitialAntihypertensive AgentsEpoprostenolHumansSurvival AnalysisTreatment OutcomeAntihypertensive AgentsEpoprostenolIdiopathic pulmonary fibrosisPrimary Pulmonary HypertensionRare lung diseases

Identifiers

PMID37979971
PMCPMC10958253
OpenAlexW4388789391

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.