Evidence map›Paper›PMID 39983052›Full record

Trial reportBlood advances2025

Improved survival with model-based dosing of antithymocyte globulin in pediatric hematopoietic cell transplantation.

Rick Admiraal, Stefan Nierkens, Marc B Bierings, Mirjam E Belderbos, Alwin D Huitema, Robbert G M Bredius, Yilin Jiang, Kevin J Curran, Andromachi Scaradavou, Maria I Cancio and 8 more

Abstract readClinical Trial, Phase II
In one paragraph

Trial report in Blood advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Trial
  3. Article
  4. Pediatric AML CAR T cell therapy.Molecular therapy. Oncology · 2026
    Review
  5. Yes, we can omit TBI for ALL!Blood advances · 2026
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
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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

18 authors.

Rick AdmiraalPediatric Blood and Marrow Transplantation Program, Princess Máxima Centre for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0003-1512-2791
Stefan NierkensPediatric Blood and Marrow Transplantation Program, Princess Máxima Centre for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0003-3406-817X
Marc B BieringsPediatric Blood and Marrow Transplantation Program, Princess Máxima Centre for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0002-0192-3080
Mirjam E BelderbosPediatric Blood and Marrow Transplantation Program, Princess Máxima Centre for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0002-6164-2918
Alwin D HuitemaDepartment of Pharmacology, Princess Máxima Centre for Pediatric Oncology, Utrecht, The Netherlands.
Robbert G M BrediusDepartment of Pediatrics, Leiden University Medical Centre, Leiden, The Netherlands.ORCID 0000-0001-8151-1539
Yilin JiangDepartment of Statistics and Bio-Analysis, Princess Máxima Centre for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0009-0003-5480-8267
Kevin J CurranStem Cell Transplantation and Cellular Therapies, Memorial Sloan Kettering Cancer Centre, New York, NY.
Andromachi ScaradavouStem Cell Transplantation and Cellular Therapies, Memorial Sloan Kettering Cancer Centre, New York, NY.ORCID 0000-0003-2425-1069
Maria I CancioStem Cell Transplantation and Cellular Therapies, Memorial Sloan Kettering Cancer Centre, New York, NY.ORCID 0000-0003-4430-6290
Elizabeth KleinStem Cell Transplantation and Cellular Therapies, Memorial Sloan Kettering Cancer Centre, New York, NY.
Wouter J KollenPediatric Blood and Marrow Transplantation Program, Princess Máxima Centre for Pediatric Oncology, Utrecht, The Netherlands.
Dorine BrestersPediatric Blood and Marrow Transplantation Program, Princess Máxima Centre for Pediatric Oncology, Utrecht, The Netherlands.
Friso G J CalkoenPediatric Blood and Marrow Transplantation Program, Princess Máxima Centre for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0001-9059-0929
A Birgitta VersluijsPediatric Blood and Marrow Transplantation Program, Princess Máxima Centre for Pediatric Oncology, Utrecht, The Netherlands.
C Michel ZwaanPediatric Blood and Marrow Transplantation Program, Princess Máxima Centre for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0001-6892-8268
Jaap Jan BoelensStem Cell Transplantation and Cellular Therapies, Memorial Sloan Kettering Cancer Centre, New York, NY.ORCID 0000-0003-2232-6952
Caroline A LindemansPediatric Blood and Marrow Transplantation Program, Princess Máxima Centre for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0002-3984-5620

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

abstractAntithymocyte globulin (ATG) is used in pediatric allogeneic hematopoietic cell transplantation (HCT) to prevent graft-versus-host disease (GVHD) and graft failure (GF). Poor T-cell recovery, associated with increased mortality, is the main toxicity of ATG. Model-based precision dosing of ATG (MBD-ATG) minimizes toxicity while maintaining efficacy. We report updated results of the single-arm phase 2 PARACHUTE trial investigating MBD-ATG, combined with real-world experience using identical MBD-ATG. Consecutive patients receiving a first T-cell-replete HCT for any indication were evaluated. Results were compared with historical patients receiving conventional fixed ATG dosing (FIX-ATG). Primary outcome was overall survival (OS). The MBD-ATG group consisted of 214 patients (58 trial patients; 156 real-world patients); 100 patients received FIX-ATG. MBD-ATG led to superior OS compared with FIX-ATG (hazard ratio [HR] for death, 0.56; 95% confidence interval [CI], 0.34-0.93; P = .026), and lower treatment-related mortality (TRM; HR, 0.51; 95% CI, 0.29-0.92; P = .025). Successful T-cell reconstitution (>0.05 × 109/L CD4+ T cells twice within 100 after HCT) was improved in MBD-ATG vs FIX-ATG (87% ± 2% vs 47% ± 5%; P < .0001). The improved T-cell reconstitution led to lower TRM (HR, 0.19; 95% CI, 0.09-0.36; P < .0001). Incidence of grade 2-4 acute GVHD was comparable, whereas chronic GVHD (HR, 0.35; 95% CI, 0.17-0.72; P = .004) and GF (HR, 0.36; 95% CI, 0.13-0.97; P = .044) were both less frequent in MBD-ATG compared with FIX-ATG. MBD-ATG results in improved OS and reduced TRM, while reducing chronic GVHD and GF. This easy-to-implement approach improves outcomes after pediatric HCT, confirmatory studies are needed. The PARACHUTE trial is registered with the Dutch Trial Register as #NL4836.

Indexed as

Antilymphocyte SerumHematopoietic Stem Cell TransplantationImmunosuppressive AgentsAdolescentChildChild, PreschoolFemaleGraft vs Host DiseaseHumansInfantMaleTransplantation ConditioningTransplantation, HomologousTreatment OutcomeAntilymphocyte SerumImmunosuppressive Agents

Identifiers

PMID39983052
PMCPMC12142804

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.