Evidence map›Paper›PMID 42656726›Full record

ArticleFrontiers in immunology2026

APDS treatment in Germany: decision criteria, costs and contribution of leniolisib to outcomes.

Ulrich Baumann, Marie-Céline Deau, Karsten Franke, Leif G Hanitsch, Georgios Sogkas, Kirsten H Herrmann, Ulrich Bosch Dos Santos, Christof Minartz, Aljoscha S Neubauer, Fabian Hauck

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

10 authors.

Ulrich BaumannImmunology Unit, Paediatric Pulmonology, Allergy and Neonatology, Hannover Medical School (MHH), Hannover, Germany.
Marie-Céline DeauInstitute for Immunodeficiency, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Karsten FrankeInstitute of Clinical Immunology, St. Marien Hospital, Siegen, Germany.
Leif G HanitschImmunodeficiency Outpatient Clinic, Institute for Medical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Georgios SogkasDepartment of Rheumatology and Immunology, Hannover Medical School (MHH), Hannover, Germany.
Kirsten H HerrmannPharming, Leiden, Netherlands.
Ulrich Bosch Dos SantosPharming, Leiden, Netherlands.
Christof MinartzInstitute for Health- and Pharmacoeconomics (IfGPh), Muenchen, Germany.
Aljoscha S NeubauerInstitute for Health- and Pharmacoeconomics (IfGPh), Muenchen, Germany.
Fabian HauckDepartment of Pediatrics, University Children's Hospital Heidelberg - Mannheim, Ruprecht-Karls-Universität, Heidelberg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Activated PI3 Kinase Delta Syndrome (APDS) is a rare inborn error of immunity. To better classify the contribution of a potential new therapeutic precision agent, leniolisib, medically relevant decision criteria were assessed upon which an outcomes model was built. Methods: Two online surveys and two roundtable discussions with 6 medical and scientific experts were conducted to obtain and discuss clinical and cost components. Based on the discussion results, key decision outcomes were modelled in an outcomes model. Results: Key decision therapeutic criteria of physicians were reliably found in two rounds of Maximum Difference Scaling, with efficacy being most important, followed by safety, disease severity, and quality of life impact. Relevant clinical outcomes in APDS, that were considered well quantifiable, were frequency of infections, lymphoproliferation, bronchiectasis, lymphoma, and mortality. For these outcomes, relevant improvements versus current standard of care were estimated for the new therapeutic precision agent leniolisib. Expert assessments in the online surveys, which were carried out by the 6 participants independently, showed low variance across participants. Ratings resulted in a projected reduction of mortality by use of leniolisib of ~16% at an age of 40 years (95% CI: [9%; 22%]). This age is currently reached only by 65% of APDS patients. Other changes were expected for costs, immunoglobulin replacement, treatment of lymphoma and other malignancies, bronchiectasis, and advanced lung disease, as well as allogeneic hematopoietic cell transplantation (alloHCT). Conclusions: Decision criteria of physicians for treating APDS are well in line with other therapeutic areas, with efficacy considered to be most relevant. Based on currently available data on leniolisib therapy, mortality and several patient-relevant morbidity endpoints are expected to improve in future clinical practice in Germany. Leniolisib may significantly modify the course of disease in APDS patients.

Indexed as

Class I Phosphatidylinositol 3-KinasesPrimary Immunodeficiency DiseasesClinical Decision-MakingCost-Benefit AnalysisGermanyHumansQuality of LifeTreatment OutcomeClass I Phosphatidylinositol 3-Kinasesactivated PI3 kinase delta syndrome (APDS)European society for immunodeficiencies (ESID)inborn error of immunity (IEI)leniolisibPI3Kδ inhibitortherapeutic decision criteria

Identifiers

PMID42656726
PMCPMC13507936

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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.