Evidence map›Paper›PMID 42750094›Full record

Trial reportJournal of immunology research2026

Associations Between Short-Term Changes in Disease Activity and Long-Term Clinical Outcomes in Activated Phosphoinositide 3-Kinase Delta Syndrome.

Joanne Tutein Nolthenius, Barbara Torlinska, Louise Linsell, Neil Hawkins, Yuxian Chen, John Whalen, Anna Šedivá

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of immunology research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Joanne Tutein NoltheniusPharming Group N.V., Leiden, Netherlands.ORCID https://orcid.org/0009-0004-9491-0845
Barbara TorlinskaVisible Analytics, Oxford, UK.
Louise LinsellVisible Analytics, Oxford, UK.
Neil HawkinsVisible Analytics, Oxford, UK.
Yuxian ChenVisible Analytics, Oxford, UK.
John WhalenPharming Group N.V., Leiden, Netherlands.
Anna ŠediváDepartment of Immunology, University Hospital Motol and Homolka, 2nd Faculty of Medicine, Charles University, Prague, Czech Republic, cuni.cz.ORCID https://orcid.org/0000-0001-7730-2304

Funding

Pharming Group N.V.
6 · The paper itself

Abstract

backgroundClinical trials in activated phosphoinositide 3-kinase delta (PI3Kδ) syndrome (APDS), an ultra-rare disease, have evaluated treatment response to the PI3Kδ inhibitor leniolisib using disease activity endpoints, including those measuring immunodeficiency and immune dysregulation. However, the relationship between disease activity endpoints and long-term clinical outcomes has not been quantified.

methodsData from a randomised controlled trial and its open-label extension (OLE) investigating leniolisib were used to evaluate associations between short-term disease activity endpoints and longer-term clinical outcomes. Both single time point and repeated measures analyses were conducted using linear regression modelling and random effects multilevel regression modelling, respectively.

resultsIn total, 39 patients were included (≤6 years of follow-up). Improvements in multiple immunodeficiency and dysregulation disease activity endpoints were significantly associated with increases in the patient global assessment (PtGA) and the 36-item short form survey (SF-36) physical component score and mental component score (PCS/MCS). Increasing proportion of naïve B cells was associated with reduction in infection rates (2.3% fewer infections per 1% increase in naïve B cells).

conclusionsIn this clinical trial setting, short-term improvements in immunodeficiency and dysregulation following treatment with leniolisib were associated with longer-term improvements in clinical outcomes, including infection rates and quality of life, for patients with APDS.

Indexed as

Class I Phosphatidylinositol 3-KinasesGenetic Diseases, X-LinkedPrimary Immunodeficiency DiseasesAdolescentAdultB-LymphocytesChildChild, PreschoolFemaleHumansMaleTreatment OutcomeClass I Phosphatidylinositol 3-KinasesAPDSclinical outcomesdisease activity endpointsinfection ratesPI3Kδ

Identifiers

PMID42750094
PMCPMC13583054

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Registered trials

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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.