Evidence map›Paper›PMID 24869942›Full record

Trial reportBlood2014

HLA-haploidentical stem cell transplantation after removal of αβ+ T and B cells in children with nonmalignant disorders.

Alice Bertaina, Pietro Merli, Sergio Rutella, Daria Pagliara, Maria Ester Bernardo, Riccardo Masetti, Daniela Pende, Michela Falco, Rupert Handgretinger, Francesca Moretta and 11 more

4 registry-linked trialsOpen access · greenAbstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 203 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
203citing papers in PubMed, 4 pooled it
29.4field-weighted citation impact, top 1% 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.

NCT01810120 phase1 / phase2completednot on this map

Phase I/II Study of Allogeneic Hematopoietic Stem Cell Transplantation From an HLA-partially Matched Family Donor After TCR Alfa Beta Negative Selection in Pediatric Patients Affected by Hematological Disorders

TypeinterventionalSponsorMariella EnocRan2012 to 2016Enrolled30ConditionsAcute Lymphoblastic Leukemia, Leukemia Acute Myeloid - AML, Non-Hodgkin Lymphoma, Myelodysplastic SyndromesArmsTCR alfa beta T cell depletion
NCT03145545 availablenot on this map

Expanded Access Protocol Using TCR Alpha/Beta T Cell/CD19+ Depleted Donor Peripheral Stem Cells

Typeexpanded_accessSponsorChildren's Hospital of PhiladelphiaConditionsLeukemia, Bone Marrow Failure Syndrome, ImmunodeficienciesArmsApha/beta T and CD19+ cell depletion using CliniMACS device
NCT04523376 nacompletednot on this mapstarted 2020, after this paper: background citation

Closely Matched Unrelated Donor Peripheral Blood Stem Cell Transplantation With TCRαβ+ T Cell and B Cell Depletion For Patients With Sickle Cell Disease and Thalassemia Major

TypeinterventionalSponsorTimothy OlsonRan2020 to 2025Enrolled8ConditionsSickle Cell Disease, Thalassemia MajorArmsCliniMACS
NCT05508009 phase1 / phase2recruitingnot on this mapstarted 2023, after this paper: background citation

Phase 1b/2a Trial of Allogeneic Hematopoietic Stem Cell Transplantation (HSCT) From an HLA-partially Matched Related or Unrelated Donor After TCRαβ+ T-cell/CD19+ B-cell Depletion for Patients Who Will Receive a Kidney Transplant (KT) From the Same HSCT/KT Donor

TypeinterventionalSponsorAlice BertainaRan2023 to 2034Enrolled12ConditionsSIOD, Cystinosis, FSGS, SLE NephritisArmsCyclophosphamide 1200 mg/Kg, Fludarabine, Cyclophosphamide 100 mg/Kg, Total Body Irradiation, ATG
3 · Its place in the literature

Who cites it

203 citing papers in PubMed, 4 syntheses or guidelines pooled it, 421 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Pooled it
  4. Guideline
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Trial
  12. Trial
  13. Trial
  14. Unrelated Donor Transplantation in Children with Thalassemia using Reduced-Intensity Conditioning: The URTH Trial.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2018
    Trial
  15. Trial
  16. Haploidentical stem cell transplantation with CD3Bone marrow transplantation · 2017
    Trial
  17. Allogeneic transplantation using CD34British journal of haematology · 2017
    Trial
  18. Trial
  19. Trial
  20. Trial

143 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 7 institutions in 3 countries.

Alice BertainaDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico Bambino Gesù Children's Hospital, Rome, Italy;
Pietro MerliDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico Bambino Gesù Children's Hospital, Rome, Italy;
Sergio RutellaDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico Bambino Gesù Children's Hospital, Rome, Italy; Department of Medical Sciences, Catholic University Medical School, Rome, Italy;
Daria PagliaraDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico Bambino Gesù Children's Hospital, Rome, Italy;
Maria Ester BernardoDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico Bambino Gesù Children's Hospital, Rome, Italy;
Riccardo MasettiDepartment of Pediatrics, Sant'Orsola Hospital, University of Bologna, Bologna, Italy;
Daniela PendeIstituto di Ricovero e Cura a Carattere Scientifico Azienda Ospedaliera Universitaria San Martino-Istituto Nazionale per la Ricerca sul Cancro, Genoa, Italy;
Michela FalcoIstituto di Ricovero e Cura a Carattere Scientifico Giannina Gaslini, Genoa, Italy;
Rupert HandgretingerChildren's University Hospital, University of Tuebingen, Tuebingen, Germany;
Francesca MorettaDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico Bambino Gesù Children's Hospital, Rome, Italy;
Barbarella LucarelliDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico Bambino Gesù Children's Hospital, Rome, Italy;
Letizia P BresciaDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico Bambino Gesù Children's Hospital, Rome, Italy;
Giuseppina Li PiraDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico Bambino Gesù Children's Hospital, Rome, Italy;
Manuela TestiLaboratory of Immunogenetics and Transplant Biology, Istituto Mediterraneo di Ematologia Foundation at Tor Vergata University Hospital, Rome, Italy;
Caterina CancriniUniversity Department of Pediatrics, Istituto di Ricovero e Cura a Carattere Scientifico Bambino Gesù Children's Hospital, University of Rome Tor Vergata, Rome, Italy;
Nabil KabbaraPediatric Hematology Oncology Division, Rafic Hariri University Hospital, Beirut, Lebanon;
Rita CarsettiDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico Bambino Gesù Children's Hospital, Rome, Italy;
Andrea FinocchiUniversity Department of Pediatrics, Istituto di Ricovero e Cura a Carattere Scientifico Bambino Gesù Children's Hospital, University of Rome Tor Vergata, Rome, Italy;
Alessandro MorettaDipartimento di Medicina Sperimentale and Centro di Eccellenza per la Ricerca Biomedica, Università di Genova, Genoa, Italy; and.
Lorenzo MorettaIstituto di Ricovero e Cura a Carattere Scientifico Giannina Gaslini, Genoa, Italy;
Franco LocatelliDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico Bambino Gesù Children's Hospital, Rome, Italy; Department of Pediatrics, University of Pavia, Pavia, Italy.
Bambino Gesù Children's Hospital · ITIstituto Giannina Gaslini · ITOspedale Policlinico San Martino · ITRafik Hariri University Hospital · LBUniversity Children's Hospital Tübingen · DEUniversity of Bologna · ITUniversity of Genoa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Twenty-three children with nonmalignant disorders received HLA-haploidentical hematopoietic stem cell transplantation (haplo-HSCT) after ex vivo elimination of αβ(+) T cells and CD19(+) B cells. The median number of CD34(+), αβ(+)CD3(+), and B cells infused was 16.8 × 10(6), 40 × 10(3), and 40 × 10(3) cells/kg, respectively. No patient received any posttransplantation pharmacologic prophylaxis for graft-versus-host disease (GVHD). All but 4 patients engrafted, these latter being rescued by a second allograft. Three patients experienced skin-only grade 1 to 2 acute GVHD. No patient developed visceral acute or chronic GVHD. Cumulative incidence of transplantation-related mortality was 9.3%. With a median follow-up of 18 months, 21 of 23 children are alive and disease-free, the 2-year probability of disease-free survival being 91.1%. Recovery of γδ(+) T cells was prompt, but αβ(+) T cells progressively ensued over time. Our data suggest that this novel graft manipulation strategy is safe and effective for haplo-HSCT. This trial was registered at www.clinicaltrials.gov as #NCT01810120.

Indexed as

B-LymphocytesHematopoietic Stem Cell TransplantationLymphocyte DepletionReceptors, Antigen, T-Cell, alpha-betaT-LymphocytesAllograftsAntigens, CDChildChild, PreschoolFemaleFollow-Up StudiesGraft vs Host DiseaseHumansInfantMaleRetrospective StudiesAntigens, CDReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID24869942
OpenAlexW2086024031

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.