Evidence map›Paper›PMID 38185663›Full record

ArticleJournal of hematology & oncology2024

Bone marrow graft versus peripheral blood graft in haploidentical hematopoietic stem cells transplantation: a retrospective analysis in1344 patients of SFGM-TC registry.

Claire Lacan, Jérôme Lambert, Edouard Forcade, Marie Robin, Patrice Chevallier, Sandrine Loron, Claude-Éric Bulabois, Corentin Orvain, Patrice Ceballos, Etienne Daguindau and 29 more

Open access · goldAbstract readLetter
In one paragraph

Article in Journal of hematology & oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
5.9field-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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
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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

39 authors at 20 institutions in 3 countries.

Claire LacanClinical Hematology Unit, Groupe Hospitalier Pitié-Salpêtrière, APHP, 47-83 Bd de l'Hôpital, 75013, Paris, France.
Jérôme LambertInstitut national de la santé et de la recherche médicale (INSERM), U1153 CRESS, Paris, France.
Edouard ForcadeClinical Hematology Unit, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
Marie RobinClinical Hematology Unit, Hôpital Saint Louis, APHP, Paris, France.
Patrice ChevallierClinical Hematology Unit, Centre Hospitalier Universitaire de Nantes, Nantes, France.
Sandrine LoronClinical Hematology Unit, Hôpital Lyon Sud, HCL, Lyon, France.
Claude-Éric BulaboisClinical Hematology Unit, Centre Hospitalier Universitaire de Grenoble, Grenoble, France.
Corentin OrvainClinical Hematology Unit, Centre Hospitalier Universitaire d'Angers, Angers, France.
Patrice CeballosClinical Hematology Unit, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.
Etienne DaguindauClinical Hematology Unit, Centre Hospitalier Universitaire de Besançon, Besançon, France.
Amandine CharbonnierClinical Hematology Unit, Centre Hospitalier Universitaire d'Amiens, Amiens, France.
Yves ChalandonClinical Hematology Unit, Hôpitaux Universitaires de Genève, Geneva, Switzerland.
Marc BernardClinical Hematology Unit, Centre Hospitalier Universitaire de Rennes, Rennes, France.
Célestine SimandClinical Hematology Unit, Institut de Cancérologie Strasbourg Europe, Strasbourg, France.
Marie-Thérèse RubioClinical Hematology Unit, Centre Hospitalier Universitaire de Nancy, Nancy, France.
Pascal TurlureClinical Hematology Unit, Centre Hospitalier Universitaire Dupuytren, Limoges, France.
Johan MaertensDepartment of Hematology, UZ Leuven, Leuven, Belgium.
Anne HuynhClinical Hematology Unit, Oncopôle, Toulouse, France.
Michael LoschiClinical Hematology Unit, Centre Hospitalier Universitaire de Nice, Nice, France.
Jacques-Olivier BayClinical Hematology Unit, Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, France.
Gaëlle GuillermClinical Hematology Unit, Centre Hospitalier Universitaire de Brest, Brest, France.
Mustafa AlaniClinical Hematology Unit, Centre Henri Becquerel, Rouen, France.
Cristina Castilla-LlorenteClinical Hematology Unit, Institut Gustave Roussy, Villejuif, France.
Xavier PoiréClinical Hematology Unit, Clinique Universitaire Saint Luc, Leuven, Belgium.
Sylvain ChantepieClinical Hematology Unit, Centre Hospitalier Universitaire de Caen, Caen, France.
Natacha MaillardClinical Hematology Unit, Centre Hospitalier Universitaire de Poitiers, Poitiers, France.
Yves BeguinClinical Hematology Unit, Centre Hospitalier Universitaire de Liège and University of Liège, Liège, Belgium.
Ambroise MarçaisClinical Hematology Unit, Hôpital Necker-Enfants Malades, APHP, Paris, France.
Jérôme CornillonClinical Hematology Unit, Centre Hospitalier Universitaire de Saint Etienne, Saint Etienne, France.
Jean-Valère MalfusonClinical Hematology Unit, Hôpitaux d'Instruction des Armées Percy, Clamart, France.
Sébastien MauryClinical Hematology Unit, Hôpital Henri Mondor, APHP, Créteil, France.
Nathalie MeulemanClinical Hematology Unit, Institut Jules Bordet, Brussels, Belgium.
Alban VillateClinical Hematology Unit, Hôpital Bretonneau, Tours, France.
Mohammed-Amine BekadjaClinical Hematology Unit, Clinic of Hematology and Cell Therapy, EHU 1St November, Oran, Algeria.
Anouk Walter-PetrichInstitut national de la santé et de la recherche médicale (INSERM), U1153 CRESS, Paris, France.
Nathalie JacqueClinical Hematology Unit, Groupe Hospitalier Pitié-Salpêtrière, APHP, 47-83 Bd de l'Hôpital, 75013, Paris, France.
Micha SrourClinical Hematology Unit, Centre Hospitalier Universitaire de Lille, Lille, France.
Raynier DevillierClinical Hematology Unit, Institut Paoli Calmette, Marseille, France.
Stéphanie NguyenClinical Hematology Unit, Groupe Hospitalier Pitié-Salpêtrière, APHP, 47-83 Bd de l'Hôpital, 75013, Paris, France. stephanie.nguyen-quoc@aphp.fr.
Sorbonne Université · FRInserm · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Universitaire Amiens-Picardie · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Caen Normandie · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Lille · FRCentre Hospitalier Universitaire de Montpellier · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Nice · FRCentre Hospitalier Universitaire de Poitiers · FRCentre Hospitalier Universitaire de Rennes · FRCentre Hospitalier Universitaire de Saint-Étienne · FRCentre Hospitalier Universitaire de Tours · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of peripheral blood (PB) or bone marrow (BM) stem cells graft in haploidentical hematopoietic stem cell transplantation with post-transplant cyclophosphamide (PTCy) for graft-versus-host disease (GVHD) prophylaxis remains controversial. Moreover, the value of adding anti-thymoglobulin (ATG) to PTCy is unknown. A total of 1344 adult patients received an unmanipulated haploidentical transplant at 37 centers from 2012 to 2019 for hematologic malignancy. We compared the outcomes of patients according to the type of graft, using a propensity score analysis. In total population, grade II-IV and III-IV acute GVHD (aGVHD) were lower with BM than with PB. Grade III-IV aGVHD was lower with BM than with PB + ATG. All outcomes were similar in PB and PB + ATG groups. Then, in total population, adding ATG does not benefit the procedure. In acute leukemia, myelodysplastic syndrome and myeloproliferative syndrome (AL-MDS-MPS) subgroup receiving non-myeloablative conditioning, risk of relapse was twice greater with BM than with PB (51 vs. 22%, respectively). Conversely, risk of aGVHD was greater with PB (38% for aGVHD II-IV; 16% for aGVHD III-IV) than with BM (28% for aGVHD II-IV; 8% for aGVHD III-IV). In this subgroup with intensified conditioning regimen, risk of relapse became similar with PB and BM but risk of aGVHD III-IV remained higher with PB than with BM graft (HR = 2.0; range [1.17-3.43], p = 0.012).

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationAdultBone MarrowCyclophosphamideHematopoietic Stem CellsHumansRecurrenceRetrospective StudiesCyclophosphamideAnti-thymoglobulinBone marrowGraft sourceHaploidentical hematopoietic stem cell transplantationPeripheral stem cell

Identifiers

PMID38185663
PMCPMC10773006
OpenAlexW4390655981

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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.