Evidence map›Paper›PMID 41376570›Full record

Trial reportHaematologica2026

HLA-haploidentical hematopoietic stem cell transplantation in patients with sickle cell disease: results from the phase II DREP-HAPLO trial.

Nathalie Dhedin, Benedicte Bruno, Catherine Paillard, Erasti Gounfle, Nimnrod Buchbinder, Marie Ouachee Chardin, Mabel Gaba, Jean-Benoit Arlet, Cecile Arnaud, Camille Jung and 1 more

Abstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Haematologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Nathalie DhedinAdolescent and Young Adult Hematology Unit, Saint Louis University Hospital, Assistance Publique-Hopitaux de Paris (AP-HP), Paris, France; Epidemiology and Clinical Statistics for Trials and Real-world evidence Research (ECSTRRA), Saint Louis Research Institute, UMR1342, INSERM, Universite de Paris. nathalie.dhedin@aphp.fr.
Benedicte BrunoPaediatric Hematology, F-59000 Lille.
Catherine PaillardDepartment of Paediatric Haematology and Oncology, Strasbourg University Hospital, Strasbourg, France; Strasbourg University, INSERM, IRM UMR-S 1109, F-67000 Strasbourg.
Erasti GounfleDepartment of Health Research and Innovation, Intercommunal Hospital Center of Creteil, Creteil.
Nimnrod BuchbinderDepartment of Paediatric Haematology and Oncology, Charles Nicolle University Hospital, Rouen.
Marie Ouachee ChardinInstitute of Pediatric Oncology and Hematology, Lyon.
Mabel GabaDepartment of Health Research and Innovation, Intercommunal Hospital Center of Creteil, Creteil.
Jean-Benoit ArletFrench Sickle Cell Referral Center, Internal Medicine Department, Georges Pompidou European Hospital, and Paris University, Paris.
Cecile ArnaudPediatric department Sickle Cell Referral Center, Centre Hospitalier Intercommunal de Creteil.
Camille JungDepartment of Health Research and Innovation, Intercommunal Hospital Center of Creteil, Creteil, France; Pediatric department Intercommunal Hospital Center of Creteil and University Paris-Est Creteil, Creteil.
Corinne PondarreIntercommunal Hospital Center of Creteil, INSERM U955, IMRB, Paris XII University, Creteil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the final analysis of the DREP-HAPLO multicenter phase II protocol, which evaluated haploidentical transplantation after a reduced-intensity conditioning regimen incorporating thiotepa, in children and adults with severe sickle cell disease (SCD). Twenty-two patients (median age, 17 years; range, 12-40) received a conditioning regimen consisting of 2 Gy total body irradiation, thymoglobulin, cyclophosphamide, fludarabine, and thiotepa, followed by T-cell-replete bone marrow infusion and graft-versus-host disease (GvHD) prophylaxis based on post-transplant cyclophosphamide. The primary endpoint, event-free survival, defined as survival without graft failure and without moderate-to-severe chronic GvHD, was 68.18% (95% confidence interval [95% CI]: 51.25%-90.70%) and 61.98% (95% CI: 44.07%-87.19%) at 1 and 4 years, respectively. Overall survival and rejection-free survival at 4 years were 90.15% (95% CI: 78.03%-100%) and 85.56% (95% CI: 71.63%- 100%), respectively. Six patients (27%) developed moderate-to-severe GVHD. In most cases (4/6) GvHD resolved, leaving only two patients (9%) with persistent moderate-to-severe GvHD at their last follow-up. Eighty-five grade 2 to 4 infectious episodes were reported in 21 patients during the 24 months of follow-up, most of which were bacterial (38 cases). These data strengthen existing evidence supporting the feasibility of haploidentical transplantation in both pediatric and adult patients with severe SCD, demonstrating a very low rejection rate when thiotepa is incorporated into the conditioning regimen. Future efforts should focus on reducing chronic GvHD and infection rates.

Indexed as

Anemia, Sickle CellHematopoietic Stem Cell TransplantationHLA AntigensAdolescentAdultChildFemaleGraft vs Host DiseaseHumansMaleTransplantation ConditioningTransplantation, HaploidenticalTreatment OutcomeYoung AdultHLA Antigens

Identifiers

PMID41376570
PMCPMC13317863

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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.