Evidence map›Paper›PMID 36097283›Full record

ArticleLeukemia2022

Incidence of subsequent malignancies after total body irradiation-based allogeneic HSCT in children with ALL - long-term follow-up from the prospective ALL-SCT 2003 trial.

Anna Eichinger, Ulrike Poetschger, Evgenia Glogova, Peter Bader, Oliver Basu, Rita Beier, Birgit Burkhardt, Carl-Friedrich Classen, Alexander Claviez, Selim Corbacioglu and 18 more

Open access · hybridAbstract read
In one paragraph

Article in Leukemia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

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  14. Knowledge and competences in hematological malignancies amongst radiation oncology residents in Germany-results from a national survey.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2024
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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

28 authors at 20 institutions in 3 countries.

Anna EichingerDepartment of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, LMU, Munich, Germany.ORCID http://orcid.org/0000-0002-2256-6633
Ulrike PoetschgerChildren's Cancer Research Institute, Vienna, Austria.
Evgenia GlogovaChildren's Cancer Research Institute, Vienna, Austria.
Peter BaderDivision for Stem Cell Transplantation and Immunology, Department for Children and Adolescents, University Hospital, Goethe University, Frankfurt/Main, Germany.ORCID http://orcid.org/0000-0003-4554-0265
Oliver BasuDepartment of Pediatrics III, University Hospital Essen, University Medicine Essen, Essen, Germany.
Rita BeierDepartment of Pediatric Oncology and Hematology, Medizinische Hochschule Hannover, Hannover, Germany.
Birgit BurkhardtPediatric Hematology and Oncology, University Hospital Muenster, Muenster, Germany.ORCID http://orcid.org/0000-0002-1151-829X
Carl-Friedrich ClassenOncology and Hematology Unit, Children's Hospital, University Medicine Rostock, Rostock, Germany.
Alexander ClaviezDepartment of Pediatrics and Bone Marrow Transplant Unit, Medical University of Schleswig-Holstein, Campus Kiel, Kiel, Germany.ORCID http://orcid.org/0000-0001-7064-8556
Selim CorbaciogluDepartment of Pediatric Hematology, Oncology and Stem Cell Transplantation, University of Regensburg, Regensburg, Germany.
Hedwig E DeubzerDepartment of Pediatric Hematology and Oncology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0002-6115-4893
Johann GreilDepartment of Pediatric Oncology, Hematology and Immunology, University of Heidelberg, Heidelberg, Germany.
Bernd GruhnDepartment of Pediatrics, Jena University Hospital, Jena, Germany.ORCID http://orcid.org/0000-0003-1862-0075
Tayfun GüngörDepartment of Hematology/Oncology/Immunology, Gene-therapy, and Stem Cell Transplantation, University Children's Hospital Zurich - Eleonore Foundation & Children's Research Center (CRC), Zurich, Switzerland.ORCID http://orcid.org/0000-0002-3261-1186
Kinan KafaDepartment of Pediatrics, University of Halle, Halle, Germany.
Jörn-Sven KühlDepartment of Pediatric Oncology, Hematology and Hemostaseology, University of Leipzig, Leipzig, Germany.
Peter LangUniversity Children's Hospital, Tübingen, Germany.ORCID http://orcid.org/0000-0001-7737-2142
Bjoern Soenke LangeDepartment of Pediatrics, University Hospital Carl Gustav Carus, Technical University of Dresden, Dresden, Germany.
Roland MeiselDivision of Pediatric Stem Cell Therapy, Department of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany.ORCID http://orcid.org/0000-0001-5230-0628
Ingo MüllerDivison of Pediatric Stem Cell Transplantation and Immunology, Clinic for Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID http://orcid.org/0000-0002-7477-6632
Martin G SauerDepartment of Pediatric Oncology and Hematology, Medizinische Hochschule Hannover, Hannover, Germany.
Paul-Gerhardt SchlegelDepartment of Pediatric Hematology and Oncology, University Children's Hospital Würzburg, Würzburg, Germany.
Ansgar SchulzDepartment of Pediatrics, University Medical Center Ulm, Ulm, Germany.ORCID http://orcid.org/0000-0002-7798-7996
Daniel StachelChildren's Hospital, Universitätsklinikum Erlangen, Erlangen, Germany.
Brigitte StrahmDivision of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0002-6086-130X
Angela WawerDepartment of Pediatrics and Children's Cancer Research Center, Kinderklinik München Schwabing, Technical University of Munich School for Medicine, Munich, Germany.
Christina Peters *St. Anna Children's Hospital, University Vienna, St. Anna Children's Cancer Research Institute, Vienna, Austria.ORCID http://orcid.org/0000-0003-0369-8515
Michael H Albert *Department of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, LMU, Munich, Germany. michael.albert@med.lmu.de.ORCID http://orcid.org/0000-0001-9143-3263
St Anna Children's Hospital · ATMedizinische Hochschule Hannover · DEEssen University Hospital · DEGoethe University Frankfurt · DEHeidelberg University · DEHeinrich Heine University Düsseldorf · DEJena University Hospital · DELMU Klinikum · DELudwig-Maximilians-Universität München · DEMax Delbrück Center · DEMünchen Klinik Schwabing · DEUniversität Hamburg · DEUniversitätsklinikum Erlangen · DEUniversitätsklinikum Würzburg · DEUniversity Children's Hospital Tübingen · DEUniversity Children's Hospital Zurich · CHUniversity Hospital Carl Gustav Carus · DEUniversity Hospital Münster · DEUniversity of Freiburg · DEUniversity of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Total body irradiation (TBI)-based conditioning is associated with superior leukemia-free survival in children with ALL undergoing HSCT. However, the risk for subsequent malignant neoplasms (SMN) remains a significant concern. We analyzed 705 pediatric patients enrolled in the prospective ALL-SCT-BFM-2003 trial and its subsequent registry. Patients >2 years received conditioning with TBI 12 Gy/etoposide (n = 558) and children ≤2 years of age or with contraindications for TBI received busulfan/cyclophosphamide/etoposide (n = 110). The 5- and 10-year cumulative incidence of SMN was 0.02 ± 0.01 and 0.13 ± 0.03, respectively. In total, 39 SMN (34 solid tumors, 5 MDS/AML) were diagnosed in 33 patients at a median of 5.8 years (1.7-13.4), exclusively in the TBI group. Of 33 affected patients, 21 (64%) are alive at a median follow-up of 5.1 years (0-9.9) after diagnosis of their first SMN. In univariate analysis, neither age at HSCT, donor type, acute GVHD, chronic GVHD, nor CMV constituted a significant risk factor for SMN. The only significant risk factor was TBI versus non-TBI based conditioning. This analysis confirms and quantifies the increased risk of SMN in children with ALL after conditioning with TBI. Future strategies to avoid TBI will need careful tailoring within prospective, controlled studies to prevent unfavorable outcomes.

Indexed as

Graft vs Host DiseaseHematopoietic Stem Cell TransplantationNeoplasmsBusulfanChildCyclophosphamideEtoposideFollow-Up StudiesHumansIncidenceProspective StudiesTransplantation ConditioningTransplantation, HomologousWhole-Body IrradiationBusulfanCyclophosphamideEtoposide

Identifiers

PMID36097283
PMCPMC9613465
OpenAlexW4295500744

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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.