Evidence map›Paper›PMID 29608607›Full record

ArticlePloS one2018

Pharmacokinetics-adapted Busulfan-based myeloablative conditioning before unrelated umbilical cord blood transplantation for myeloid malignancies in children.

Joy Benadiba, Marc Ansari, Maja Krajinovic, Marie-France Vachon, Michel Duval, Pierre Teira, Sonia Cellot, Henrique Bittencourt

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
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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

8 authors at 3 institutions in 3 countries.

Joy BenadibaDepartment of Hemato-Oncology Pediatric, Nice University Hospital, Nice, France.ORCID 0000-0003-4229-7749
Marc AnsariDepartment of Pediatrics, Geneva University Hospital, Geneva, Switzerland.
Maja KrajinovicHematology-Oncology Division - Centre de Cancérologie Charles-Bruneau, Ste-Justine Hospital, Montréal, Canada.
Marie-France VachonHematology-Oncology Division - Centre de Cancérologie Charles-Bruneau, Ste-Justine Hospital, Montréal, Canada.
Michel DuvalHematology-Oncology Division - Centre de Cancérologie Charles-Bruneau, Ste-Justine Hospital, Montréal, Canada.
Pierre TeiraHematology-Oncology Division - Centre de Cancérologie Charles-Bruneau, Ste-Justine Hospital, Montréal, Canada.
Sonia CellotHematology-Oncology Division - Centre de Cancérologie Charles-Bruneau, Ste-Justine Hospital, Montréal, Canada.
Henrique BittencourtHematology-Oncology Division - Centre de Cancérologie Charles-Bruneau, Ste-Justine Hospital, Montréal, Canada.
Centre Hospitalier Universitaire Sainte-Justine · CACentre Hospitalier Universitaire de Nice · FRUniversity of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Unrelated umbilical cord blood transplantation (UCBT) is an alternative to provide transplants in children with acute leukemia or myelodysplastic syndrome who lack a related donor. Intravenous Busulfan (Bu) combined with therapeutic drug monitoring-guided dosing has been increasingly used, with more predictable bioavailability and better outcomes comparing to oral Bu. There is still an important variation in Bu pharmacokinetic between patients that is associated with an increased risk of toxicity and graft failure. The objective of the study was to analyze the impact of first-dose pharmacokinetic adapted myeloablative conditioning regimen of intravenous Bu on the different outcomes after transplantation. Data of 36 children who underwent allogeneic HSCT with Bu plus a second alkylating agent at Sainte Justine Hospital in Montreal, Canada, between December 2000 and April 2012 were analyzed. For children with high risk myeloid malignancies receiving an UCBT, first dose Bu pharmacokinetic seems to be a significant prognostic factor, influencing neutrophil (100% vs 67.9%) and platelet recovery (95.5% vs 70.5%), non-relapse mortality (0% vs 18.6%), EFS (64% vs 28.6%) and OS (81.3% vs 37.5%) for a first-dose steady-state concentration (Css) <600ng/mL vs >600ng/mL, respectively. These data reinforce the importance of Busulfan therapeutic drug monitoring-guided dosing in pediatric HSCT patients, particularly in the context of UCBT.

Indexed as

AdolescentBusulfanChildChild, PreschoolCord Blood Stem Cell TransplantationCyclophosphamideFemaleHumansInfantLeukemia, Myeloid, AcuteMaleMyeloablative AgonistsMyelodysplastic SyndromesPrognosisTransplantation ConditioningTreatment OutcomeBusulfanCyclophosphamideMyeloablative Agonists

Identifiers

PMID29608607
PMCPMC5880335
OpenAlexW2795663728

What OpenQuestion holds

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LicenceCC BY
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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.