Evidence map›Paper›PMID 40983033›Full record

ArticleBlood2026

Hematopoietic stem cell transplantation for purine nucleoside phosphorylase deficiency: an EBMT-IEWP retrospective study.

Uli S Herrmann, Matthias Felber, Austen Worth, Sule Haskologlu, Figen Dogu, Victor A Lewis, Brigitte Strahm, Andreas Groll, Andrew R Gennery, Fabian Hauck and 29 more

Abstract readMulticenter Study
In one paragraph

Article in Blood, 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

The trial behind it

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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

5 · Who and what money

Authors and funding

39 authors.

Uli S HerrmannDepartment of Stem Cell Transplantation, University Children's Hospital, Zurich, Switzerland.ORCID 0000-0002-1327-5199
Matthias FelberDepartment of Stem Cell Transplantation, University Children's Hospital, Zurich, Switzerland.
Austen WorthDepartment of Immunology and Gene Therapy, Great Ormond Street Hospital, London, United Kingdom.ORCID 0000-0001-6803-7385
Sule HaskologluDepartment of Pediatric Immunology and Allergy, Ankara University Medical School, Ankara, Turkey.ORCID 0000-0002-2668-0441
Figen DoguDepartment of Pediatric Immunology and Allergy, Ankara University Medical School, Ankara, Turkey.ORCID 0000-0002-7869-4941
Victor A LewisDepartment of Pediatric Oncology and Blood and Marrow Transplant, Alberta Children's Hospital, University of Calgary Cumming School of Medicine, Calgary, Canada.
Brigitte StrahmDepartment of Pediatric Hematology, Oncology and Stem Cell Transplantation, Children's Hospital, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID 0000-0002-6086-130X
Andreas GrollDepartment of Hematology/Oncology/Bone Marrow Transplantation, University Children's Hospital, Münster, Germany.ORCID 0000-0003-1188-393X
Andrew R GenneryInstitute of Cellular Medicine, Child Health, University of Newcastle upon Tyne, Newcastle Upon Tyne, United Kingdom.
Fabian HauckDepartment of Pediatric Hematology and Oncology, Dr. von Hauner Children's University Hospital, Ludwig Maximilian University, Munich, Germany.ORCID 0000-0001-9644-2003
Robert WynnDepartment of Blood and Marrow Transplant, Royal Manchester Children's Hospital, Manchester, United Kingdom.ORCID 0000-0002-6046-8428
Mary CoussonsDepartment of Blood and Marrow Transplant, Royal Manchester Children's Hospital, Manchester, United Kingdom.
Isabelle MeytsDepartment of Microbiology, Immunology and Transplantation, Katholieke Universiteit, Leuven, Belgium.ORCID 0000-0003-1214-0302
Caroline LindemansPediatric Blood and Marrow Transplantation Program, Princess Máxima Centre for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0002-3984-5620
Victoria BordonDepartment of Pediatric Hemato-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent, Belgium.
Robbert G M BrediusDepartment of Pediatrics, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-8151-1539
Jörn-Sven KühlDepartment of Pediatric Hematology/Oncology/Hemostaseology, Leipzig University Hospital, Leipzig, Germany.
Mirjam VöllerDepartment of Pediatric Respiratory Medicine, Immunology and Critical Care Medicine, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
Felix ZirngiblDepartment of Pediatric Oncology and Hematology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.ORCID 0000-0003-1764-4841
Irina ZaidmanDepartment of Pediatric Hematology Oncology, Hadassah Medical Center, Jerusalem, Israel.
Alexandra LaberkoDepartment of Immunology, Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.ORCID 0000-0002-2354-2588
Ulrike ZeilhoferDepartment of Stem Cell Transplantation, University Children's Hospital, Zurich, Switzerland.
Mathias Hauri-HohlDepartment of Stem Cell Transplantation, University Children's Hospital, Zurich, Switzerland.ORCID 0000-0003-4618-3319
Arjan LankesterWillem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, The Netherlands.
Aydan IkinciogullariDepartment of Pediatric Immunology and Allergy, Ankara University Medical School, Ankara, Turkey.ORCID 0000-0003-1145-0843
Gregory M T GuilcherDepartment of Pediatric Oncology and Blood and Marrow Transplant, Alberta Children's Hospital, University of Calgary Cumming School of Medicine, Calgary, Canada.
Annette HackenbergDepartment of Pediatric Neurology, University Children`s Hospital, Zurich, Switzerland.ORCID 0000-0003-3161-8703
Akif YeşilipekDepartment of Pediatric Hematology and Oncology, Clinic Medical Park Antalya Hospital, Antalya, Turkey.
Graham DaviesDepartment of Immunology and Gene Therapy, Great Ormond Street Hospital, London, United Kingdom.
Kanchan RaoDepartment of Blood and Bone Marrow Transplantation, Great Ormond Street Hospital, London, United Kingdom.
Michael Steven HershfieldDivision of Pediatric Blood and Marrow Transplantation, Duke University Medical Center, Durham, NC.
Suhag H ParikhDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA.ORCID 0000-0002-6066-9852
Patrick GilbertEuropean Society of Blood and Marrow Transplantation, Leiden Study Unit, Leiden, The Netherlands.
Claudia Bettoni da Cunha RiehmDepartment of Pediatric Hematology and Oncology, Medical School Hannover, Hannover, Germany.
Michael H AlbertDepartment of Pediatric Hematology and Oncology, Dr. von Hauner Children's University Hospital, Ludwig Maximilian University, Munich, Germany.ORCID 0000-0001-9143-3263
Ansgar S SchulzDepartment of Pediatrics, University Medical Center Ulm, Ulm, Germany.ORCID 0000-0002-7798-7996
Manfred HönigDepartment of Pediatrics, University Medical Center Ulm, Ulm, Germany.
Bénédicte NevenDepartment of Immunology and Stem Cell Transplantation, Hôpital Necker Enfants Malades, Paris, France.
Tayfun GüngörDepartment of Stem Cell Transplantation, University Children's Hospital, Zurich, Switzerland.ORCID 0000-0002-3261-1186

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractPurine nucleoside phosphorylase (PNP) deficiency causes inadequate purine metabolite detoxification, which leads to combined immunodeficiency and variable neurologic symptoms. Hematopoietic stem cell transplantation (HSCT) cures the immunodeficiency, but large studies on the long-term outcomes are lacking. In a retrospective study of the European Society for Blood and Marrow Transplantation, we investigated 46 patients with PNP deficiency from 21 centers. We analyzed the presenting clinical signs and outcomes after HSCT. Cognition (0-3), hearing (0-3), interaction (0-4), movement (0-4), and occupation (0-3) (CHIMO) were scored at the last follow-up (FU) visit (no impairment, 17; mild, 15-16; moderate, 12-14; and severe impairment, <12). The median age at initial presentation was 7.5 (1-48) months. The patients presented with infections (41%), neurological dysfunction (39%), both (15%), or autoimmune disease (5%). At the time of HSCT (median age, 26 [2-192] months), neurological abnormalities were observed in 88% of patients. After a median FU of 7.9 (1.0-22.3) years, 40 patients were alive with a 3-year overall survival (OS)/event-free survival (EFS) probabilities of 86% (confidence interval [CI], 77%-97%)/75% (CI, 64%-89%), respectively. High-level (>50%-100%)/low-level donor chimerism (11%-50%) was observed in 85%/15% of patients, respectively, leading to resolution of T lymphopenia. The median overall CHIMO score was 14 (6-17), while the median scores for each component were 3 (0-3), 3 (1-3), 4 (1-4), 3 (1-4), and 2 (0-3), respectively. Patients who underwent HSCT before 24 months after the initial presentation demonstrated superior OS (P = .049). Neurological symptoms that occurred before 11 months of age were associated with reduced OS (P = .027). While the overall results were satisfactory, earlier diagnosis could further improve outcomes.

Indexed as

Hematopoietic Stem Cell TransplantationPurine-Nucleoside PhosphorylasePurine-Pyrimidine Metabolism, Inborn ErrorsAdolescentChildChild, PreschoolFemaleHumansInfantMalePrimary Immunodeficiency DiseasesRetrospective StudiesPurine-Nucleoside Phosphorylase

Identifiers

PMID40983033
PMCPMC12824669

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