Evidence map›Paper›PMID 33064008›Full record

ArticleJournal of proteome research2021

Prediction of Acute Graft versus Host Disease and Relapse by Endogenous Metabolomic Compounds in Patients Receiving Personalized Busulfan-Based Conditioning.

Jeannine S McCune, Jožefa S McKiernan, Erik van Maarseveen, Alwin D R Huitema, Timothy W Randolph, H Joachim Deeg, Ryotaro Nakamura, K Scott Baker

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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

8 authors at 4 institutions in 2 countries.

Jeannine S McCuneCity of Hope, Department of Population Sciences, Duarte, California 91010, United States.ORCID 0000-0002-0795-497X
Jožefa S McKiernanCity of Hope, Department of Population Sciences, Duarte, California 91010, United States.
Erik van MaarseveenDepartment of Clinical Pharmacy, University Medical Center Utrecht, Utrecht University, 3584 CS Utrecht, The Netherlands.
Alwin D R HuitemaDepartment of Clinical Pharmacy, University Medical Center Utrecht, Utrecht University, 3584 CS Utrecht, The Netherlands.
Timothy W RandolphClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, United States.
H Joachim DeegClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, United States.
Ryotaro NakamuraCity of Hope, Department of Hematology & HCT, Duarte, California 91010, United States.
K Scott BakerClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, United States.
City of Hope · USUniversity of Washington · USUtrecht University · NLFred Hutch Cancer Center · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
VIRUS-MEDIATED MYELOSUPPRESSIONP01CA018029 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI STEPHANIE J LEE · 1985 to 2026
$128.4M
Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI XIWEI WU · 1985 to 2026
$86.3M
Optimizing Busulfan: Efficacy, Toxicity, and PharmacometabolomicsR01CA182963 · NCI · UNIVERSITY OF WASHINGTON · PI MCCUNE, JEANNINE S · 2014 to 2018
$2.5M
NCATS NIH HHS UL1 TR002319NCI NIH HHS P01 CA018029NCI NIH HHS P30 CA015704NCI NIH HHS P30 CA033572NCI NIH HHS R01 CA182963
6 · The paper itself

Abstract

Busulfan-based conditioning is the most commonly used high-dose conditioning regimen for allogeneic hematopoietic cell transplant (HCT). The alkylating agent busulfan has a narrow therapeutic index, with busulfan doses personalized to a target plasma exposure (targeted busulfan). Using a global pharmacometabonomics approach, we sought to identify novel biomarkers of relapse or acute graft versus host disease (GVHD) in a cohort of 84 patients receiving targeted busulfan before allogeneic HCT. A total of 763 endogenous metabolomic compounds (EMCs) were quantitated in 230 longitudinal blood samples before, during, and shortly after intravenous busulfan administration. We performed both univariate linear regression and pathway enrichment analyses using global testing. The cysteine/methionine pathway and the glycine, serine, and threonine metabolism pathway were most associated with relapse. The latter be explained by the fact that glutathione

Indexed as

BusulfanGraft vs Host DiseaseHematopoietic Stem Cell TransplantationMetabolomicsHumansPrognosisRecurrenceTransplantation ConditioningVidarabineBusulfanVidarabineacute GVHDbiomarkersbusulfanhematopoietic cell transplantmetabolomicspharmacometabonomicsprecision medicinerelapsetherapeutic drug monitoring

Identifiers

PMID33064008
PMCPMC8214873
OpenAlexW3093055583

What OpenQuestion holds

Textmetadata
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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.