Evidence map›Paper›PMID 32753706›Full record

ArticleBone marrow transplantation2021

The impact of donor type on the outcome of pediatric patients with very high risk acute lymphoblastic leukemia. A study of the ALL SCT 2003 BFM-SG and 2007-BFM-International SG.

Jean-Hugues Dalle, Adriana Balduzzi, Peter Bader, Anna Pieczonka, Isaac Yaniv, Arjan Lankester, Marc Bierings, Akif Yesilipek, Petr Sedlacek, Marianne Ifversen and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Bone marrow transplantation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 14 citations in OpenAlex.

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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

17 authors at 14 institutions in 13 countries.

Jean-Hugues DalleDepartment of Pediatric Hemato-Immunology, Hôpital Robert Debré, APHP Nord-Université de Paris, Paris, France. jean-hugues.dalle@aphp.fr.ORCID http://orcid.org/0000-0002-8406-0793
Adriana BalduzziClinica Pediatrica, Università degli Studi di Milano Bicocca, Fondazione MBBM/Ospedale San Gerardo, Monza, Italy.ORCID http://orcid.org/0000-0002-5879-0610
Peter BaderDivision for Stem Cell Transplantation and Immunology, Department for Children and Adolescents, University Hospital Frankfurt, Goethe University, Frankfurt am Main, Germany.
Anna PieczonkaPoznan University of Medical Sciences, Depratment of Pediatric Oncology, Hematology and HSCT, Poznan, Poland.ORCID http://orcid.org/0000-0001-5922-4242
Isaac YanivThe Raina Zaizov Pediatric Hematology Oncology Division, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.
Arjan LankesterWillem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, the Netherlands.
Marc BieringsDepartment of Hematology, University Hospital of Children, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-0192-3080
Akif YesilipekPediatric Stem Cell Transplantation Unit, Medical Park Antalya Hospital, Antalya, Turkey.
Petr SedlacekDepartment of Paediatric Haematology and Oncology, University Hospital Motol, Prague, Czech Republic.
Marianne IfversenRigshospitalet, Paediatric Clinic II, Copenhagen, Denmark.
Peter SvecDepartment of Paediatric Haematology and Oncology, Haematopoietic Stem Cell Transplantation Unit, Comenius University Children's Hospital, Bratislava, Slovakia.ORCID http://orcid.org/0000-0002-7647-2253
Jacek ToporskiDepartment of Hematology, Skanes University Hopsital, Lund, Sweden.ORCID http://orcid.org/0000-0001-6012-0651
Taifun GungorPediatric Stem Cell Transplantation, UZH, University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-3261-1186
Jacek WachowiakWillem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, the Netherlands.
Evgenia GlogovaSt Anna Children's Hospital, Universitätsklinik für Kinder- und Jugendheilkunde, Medizinische Universität Wien, Vienna, Austria.
Ulrike PoetschgerSt Anna Children's Hospital, Universitätsklinik für Kinder- und Jugendheilkunde, Medizinische Universität Wien, Vienna, Austria.
Christina PetersSt Anna Children's Hospital, Universitätsklinik für Kinder- und Jugendheilkunde, Medizinische Universität Wien, Vienna, Austria.ORCID http://orcid.org/0000-0003-0369-8515
St Anna Children's Hospital · ATLeiden University Medical Center · NLAntalya IVF · TRComenius University Bratislava · SKGoethe University Frankfurt · DEPoznan University of Medical Sciences · PLRigshospitalet · DKSchneider Children's Medical Center · ILSkåne University Hospital · SEUniversité Paris Cité · FRUniversity Hospital in Motol · CZUniversity of Milano-Bicocca · ITUniversity of Zurich · CHWilhelmina Children's Hospital · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allogeneic HSCT represents the only potentially curative treatment for very high risk (VHR) ALL. Two consecutive international prospective studies, ALL-SCT-(I)BFM 2003 and 2007 were conducted in 1150 pediatric patients. 569 presented with VHR disease leading to any kind of HSCT. All patients >2 year old were transplanted after TBI-based MAC. The median follow-up was 5 years. 463 patients were transplanted from matched donor (MD) and 106 from mismatched donor (MMD). 214 were in CR1. Stem cell source was unmanipulated BM for 330 patients, unmanipulated PBSC for 135, ex vivo T-cell depleted PBSC for 62 and cord-blood for 26. There were more advanced disease, more ex vivo T-cell depletion, and more chemotherapy based conditioning regimen for patients transplanted from MMD as compared to those transplanted from MSD or MD. Median follow up (reversed Kaplan Meier estimator) was 4.99 years, median follow up of survivals was 4.88, range (0.01-11.72) years. The 4-year CI of extensive cGvHD was 13 ± 2% and 17 ± 4% (p = NS) for the patients transplanted from MD and MMD, respectively. 4-year EFS was statistically better for patients transplanted from MD (60 ± 2% vs. 42 ± 5%, p < 0.001) for the whole cohort. This difference does not exist if considering separately patients treated in the most recent study. There was no difference in 4-year CI of relapse. The 4-year NRM was lower for patients transplanted from MD (9 ± 1% vs. 23 ± 4%, p < 0.001). In multivariate analysis, donor-type appears as a negative risk-factor for OS, EFS, and NRM. This paper demonstrates the impact of donor type on overall results of allogeneic stem cell transplantation for very-high risk pediatric acute lymphoblastic leukemia with worse results when using MMD stem cell source.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationPrecursor Cell Lymphoblastic Leukemia-LymphomaChildChild, PreschoolHumansProspective StudiesRetrospective StudiesTissue DonorsTransplantation ConditioningTreatment Outcome

Identifiers

PMID32753706
PMCPMC7796856
OpenAlexW3047469812

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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.