Evidence map›Paper›PMID 41632689›Full record

ArticleBlood advances2026

Allogeneic HSCT for consolidation in pediatric refractory or relapsed ALK-positive anaplastic large cell lymphoma.

Fabian Knörr, Martin Zimmermann, Peter Bader, Peter Lang, Ingo Müller, Oliver Basu, Birgit Burkhardt, Jakob Seidl, Christine Damm-Welk, Herbert Pichler and 4 more

Abstract read
In one paragraph

Article in Blood advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Fabian KnörrPediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0003-1831-3702
Martin ZimmermannPediatric Registry for Stem Cell Transplantation and Cell Therapies, Clinical Department for Pediatric Hematology and Oncology, Hannover Medical School, Hannover, Germany.
Peter BaderDivision of Stem Cell Transplantation and Immunology, Department of Pediatrics, Goethe University Frankfurt, Frankfurt, Germany.
Peter LangDepartment of Pediatric Hematology and Oncology, University Children's Hospital, Eberhard Karls University Tuebingen, Tuebingen, Germany.
Ingo MüllerDivision of Pediatric Stem Cell Transplantation and Immunology, Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-7477-6632
Oliver BasuDepartment of Pediatrics III, University Medicine Essen, Essen, Germany.ORCID 0009-0005-9574-2449
Birgit BurkhardtPediatric Hematology and Oncology, University Hospital Muenster, Muenster, Germany.ORCID 0000-0002-1151-829X
Jakob SeidlDepartment of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.ORCID 0009-0008-3911-7501
Christine Damm-WelkPediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Herbert PichlerDepartment of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-5107-5123
Andishe AttarbaschiDepartment of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-9285-6898
Barbara MeissnerPediatric Registry for Stem Cell Transplantation and Cell Therapies, Clinical Department for Pediatric Hematology and Oncology, Hannover Medical School, Hannover, Germany.ORCID 0000-0002-5242-5559
Rita BeierPediatric Registry for Stem Cell Transplantation and Cell Therapies, Clinical Department for Pediatric Hematology and Oncology, Hannover Medical School, Hannover, Germany.ORCID 0000-0002-7568-8749
Wilhelm WoessmannPediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-6315-0888

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractAllogeneic hematopoietic stem cell transplantation (HSCT) is used for consolidation in children and adolescents with refractory or early relapsed ALK (anaplastic lymphoma kinase)-positive anaplastic large cell lymphoma (ALCL). The immune system plays a major role in sustained disease control. We retrospectively analyzed whether conditioning, donor type, and in vivo T-cell depletion correlate with outcome in a population-based cohort of 57 children with central nervous system (CNS)-negative ALCL relapse who received HSCT between 2005 and 2022. Progression-free survival (PFS) and overall survival from transplantation were 84% ± 10% and 91% ± 8% at 3 years, respectively. Conditioning was based on total body irradiation (TBI) in 30 patients and on chemotherapy in 27 patients, mainly with reduced-toxicity conditioning (treosulfan, fludarabine, and thiotepa). PFS and graft-versus-host disease (GVHD)-free and event-free survival (GEFS) were comparable between TBI and chemotherapy, 87% ± 6% vs 81% ± 8% (P = .62) and 67% ± 9% vs 74% ± 8% (P = .63), respectively. Patients with transplantation from unrelated donors with rabbit anti-human T lymphocyte globulin (ATLG) had superior PFS and GEFS than those receiving grafts from matched siblings without ATLG: 94% ± 7% vs 67% ± 22% (P = .0007) and 82% ± 13% vs 44% ± 24% (P = .011), respectively. Progression during frontline chemotherapy, minimal residual disease, and remission status at HSCT were not associated with outcome. Nonrelapse mortality was 5.6% for all 65 patients, and cumulative incidence of grade 2 to 4 acute GVHD was 25%. Our data supports the use of TBI-free conditioning and suggest improved outcomes with unrelated donors receiving ATLG prophylaxis.

Indexed as

Anaplastic Lymphoma KinaseHematopoietic Stem Cell TransplantationLymphoma, Large-Cell, AnaplasticAdolescentChildChild, PreschoolFemaleGraft vs Host DiseaseHumansMaleRecurrenceRetrospective StudiesTransplantation ConditioningTransplantation, HomologousALK protein, humanAnaplastic Lymphoma Kinase

Identifiers

PMID41632689
PMCPMC13101688

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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.