Evidence map›Paper›PMID 30181580›Full record

ArticleBone marrow transplantation2020

Veno-occlusive disease after high-dose busulfan-melphalan in neuroblastoma.

Tal Schechter, Evelio Perez-Albuerne, Tiffany F Lin, Meredith S Irwin, Mohammed Essa, Ami V Desai, Haydar Frangoul, Gregory Yanik, L Lee Dupuis, David Jacobsohn and 6 more

Abstract read
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Observational
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Risk Factors for Transplant-Associated Thrombotic Microangiopathy after Autologous Hematopoietic Cell Transplant in High-Risk Neuroblastoma.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Article
  11. Review
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

16 authors at 11 institutions in 3 countries.

Tal SchechterDivision of Hematology/Oncology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada. tal.schechter-finkelstein@sickkids.ca.
Evelio Perez-AlbuerneDivision of Stem-Cell Transplant, Children's National Health System, George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
Tiffany F LinDepartment of Pediatrics, University of California San Francisco Benioff Children's Hospital, San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-0676-2626
Meredith S IrwinDivision of Hematology/Oncology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Mohammed EssaDepartment of Pediatric Haematology/Oncology, King Abdullah Specialized Children's Hospital, King Saud bin Abdulaziz University for Health Sciences, Ministry of National Guard, Riyadh, Saudi Arabia.
Ami V DesaiDepartment of Pediatrics, Section of Hematology/Oncology & Stem Cell Transplantation, The University of Chicago, Chicago, IL, USA.
Haydar FrangoulPediatric Stem Cell Transplant Program The Children's Hospital, TriStar Centennial and Sarah Cannon Research Institute, Nashville, TN, USA.
Gregory YanikDivision of Hematology Oncology, Department of Pediatrics, C.S. Mott Children's Hospital, University of Michigan, Ann Arbor, MI, USA.
L Lee DupuisDepartment of Pharmacy and Research Institute, The Hospital for Sick Children, Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-7699-1061
David JacobsohnDivision of Stem-Cell Transplant, Children's National Health System, George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
Morris KletzelPediatric Hematology, Oncology and Stem Cell Transplantation, Northwestern University Feinberg School of Medicine, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.ORCID http://orcid.org/0000-0002-9862-510X
Mark RanalliDivision of Hematology/Oncology/Bone Marrow Transplantation Nationwide Children's Hospital, The Ohio State University College of Medicine, Columbus, OH, USA.
Sandeep SoniDivision of Stem Cell Transplant, Department of Pediatrics, Lucile Packard Children's Hospital, Stanford University, Palo Alto, CA, USA.
Alix E SeifDivision of Oncology, Children's Hospital of Philadelphia, Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0002-1799-2582
Stephan GruppDivision of Oncology, Children's Hospital of Philadelphia, Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA, USA.
Christopher C DvorakDepartment of Pediatrics, University of California San Francisco Benioff Children's Hospital, San Francisco, CA, USA.
University of Toronto · CAChildren's Hospital of Philadelphia · USChildren's National · USUniversity of California, San Francisco · USChildren’s Hospital at TriStar Centennial · USKing Saud bin Abdulaziz University for Health Sciences · SALucile Packard Children's Hospital · USNationwide Children's Hospital · USNorthwestern University · USUniversity of Chicago · USUniversity of Michigan · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Survival for high-risk neuroblastoma patients is still suboptimal. Although stem cell transplantation (SCT) is used, there is no consensus as to which conditioning regimen has the greatest efficacy and fewest toxicities. We assessed the incidence of and risk for hepatic veno-occlusive disease (VOD) for neuroblastoma patients who underwent autologous SCT with busulfan and melphalan (BuMel) at eight centers following Children's Oncology Group (COG)-based induction chemotherapy. Data regarding the patients, SCT characteristics, busulfan steady-state concentrations, incidence of VOD, and survival were evaluated. VOD was defined using the modified Seattle criteria. Possible factors associated with VOD (age, busulfan-pharmacokinetic parameters, history of hepatic dysfunction, and day of neutrophil engraftment) were evaluated. Seventy five patients were included and 23 children (31%) developed VOD at a median of 19 days after SCT (range 14-27 days). VOD was the cause of death in 4 patients (5%). In a multivariable analysis, young age (OR 1.7 (95% CI: 1.16-2.56; p = 0.012)) and early day of neutrophil engraftment (OR 1.4 (95% CI: 1.08-2.14; p = 0.041) were associated with the development of VOD. Initial or cumulative busulfan steady-state concentration were not associated with VOD. We found that despite the use of intravenous busulfan with adjusted serum levels, the incidence of VOD remains high in pediatric neuroblastoma patients.

Indexed as

Hematopoietic Stem Cell TransplantationHepatic Veno-Occlusive DiseaseNeuroblastomaBusulfanChildHumansMelphalanTransplantation ConditioningBusulfanMelphalan

Identifiers

PMID30181580
OpenAlexW2891765344

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.