Evidence map›Paper›PMID 42028818›Full record

Observational studyHaemophilia : the official journal of the World Federation of Hemophilia

Real-World Effectiveness and Safety of Concizumab Prophylaxis in Hemophilia: Results From a National French Cohort.

Caroline Galeotti, Antoine Rauch, Helene Gatti, Stephanie Desage, Alexandre Butelet, Christine Biron-Andreani, Sophie Susen, Roseline d'Oiron, Guillaume Chanteau, Valerie Proulle and 1 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Haemophilia : the official journal of the World Federation of Hemophilia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Observational
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.

Caroline GaleottiCentre De Référence de L'hémophilie Et Des Maladies Hémorragiques Rares, Hôpital Bicêtre, Université Paris-Saclay, Le KremlinBicêtre, France.
Antoine RauchHématologie-transfusion, CHU De Lille, Lille, France.
Helene GattiService De Pédiatrie, Hopital Taaone, Pirae, Polynesie Francaise.
Stephanie DesageCentre De Reference de L'hemophilie - Unite d'Hemostase Clinique, Hopital Louis Pradel Et UR4609 Hemostase & Thrombose Universite Lyon 1, Lyon, France.
Alexandre ButeletService Hématologie Biologique, UF Hémostase clinique, Hôpital Robert, Debré, CHU Reims, France.
Christine Biron-AndreaniCentre De Ressources et De Compétences - Maladies Hémorragiques rares, Service D'hématologie Biologique, CHU De Montpellier, Montpellier, France.
Sophie SusenHématologie-transfusion, CHU De Lille, Lille, France.
Roseline d'OironCentre De Référence de L'hémophilie Et Des Maladies Hémorragiques Rares, Hôpital Bicêtre, Université Paris-Saclay, Le KremlinBicêtre, France.
Guillaume ChanteauHematologie Clinique, Hopital Taaone, PAPEETE, Polynesie Francaise.
Valerie ProulleService Hématologie Biologique, UF Hémostase clinique, Hôpital Robert, Debré, CHU Reims, France.
Yesim DargaudCentre De Reference de L'hemophilie - Unite d'Hemostase Clinique, Hopital Louis Pradel Et UR4609 Hemostase & Thrombose Universite Lyon 1, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInhibition of tissue factor pathway inhibitor represents an advanced rebalancing strategy for hemophilia, applicable across hemophilia A and B irrespective of inhibitor status. Although concizumab has demonstrated efficacy in clinical trials, real-world data remain very limited.

objectivesTo evaluate the real-world effectiveness and safety of concizumab prophylaxis in an unselected national cohort of patients treated in routine clinical practice in France.

methodsThis cross-sectional observational study included all patients receiving concizumab through compassionate-use or Early Access Programs across six French hemophilia centers. Retrospective data were collected from treatment initiation to a predefined cutoff (1, December 2025). Outcomes included bleeding rates, target joint status, surgical management, laboratory monitoring practices, adherence, and adverse events.

resultsEleven patients were included, ten with hemophilia B with inhibitors and one with hemophilia B without inhibitors. Mean exposure to concizumab was 22.8 months. Compared with the pre-treatment period, concizumab prophylaxis was associated with a marked reduction in bleeding, including complete absence of bleeding in four patients and resolution of target joints in nine of ten patients. Nine surgical procedures, including two major surgeries, were performed under concizumab prophylaxis with concomitant rFVIIa without thrombotic complications. No thrombotic events or injection-site pain were reported. None of the patients discontinued concizumab prophylaxis.

conclusionsIn this nationwide real-world cohort, concizumab prophylaxis was effective, well tolerated, and manageable in routine practice, including during surgical procedures. These data support its use as a valuable prophylactic option in carefully selected patients with hemophilia B and inhibitors, while underscoring the importance of individualized monitoring and thrombotic risk assessment.

Indexed as

Antibodies, Monoclonal, HumanizedHemophilia AHemophilia BAdolescentAdultChildChild, PreschoolCohort StudiesCross-Sectional StudiesFemaleFranceHemorrhageHumansMaleMiddle AgedRetrospective StudiesAntibodies, Monoclonal, Humanizedconcizumabanti‐TFPI antibodyconcizumabhemophiliahemophilia Binhibitorsrebalancing agents

Identifiers

PMID42028818
PMCPMC13378656

What OpenQuestion holds

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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.