Evidence map›Paper›PMID 38611035›Full record

ArticleCancers2024

Using Targeted Transcriptome and Machine Learning of Pre- and Post-Transplant Bone Marrow Samples to Predict Acute Graft-versus-Host Disease and Overall Survival after Allogeneic Stem Cell Transplantation.

Scott D Rowley, Thomas S Gunning, Michael Pelliccia, Alexandra Della Pia, Albert Lee, James Behrmann, Ayrton Bangolo, Parul Jandir, Hong Zhang, Sukhdeep Kaur and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2024. 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
4.1field-weighted citation impact, top 6% 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. Review
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  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

14 authors at 3 institutions in 1 country.

Scott D RowleyGeorgetown University School of Medicine, Washington, DC 20007, USA.ORCID 0000-0002-3299-835X
Thomas S GunningHackensack Meridian School of Medicine, Nutley, NJ 07110, USA.ORCID 0000-0001-8116-8136
Michael PellicciaHackensack Meridian School of Medicine, Nutley, NJ 07110, USA.
Alexandra Della PiaJohn Theurer Cancer Center, Hackensack, NJ 07601, USA.ORCID 0000-0003-0875-6489
Albert LeeHackensack Meridian School of Medicine, Nutley, NJ 07110, USA.
James BehrmannHackensack Meridian School of Medicine, Nutley, NJ 07110, USA.ORCID 0000-0001-5281-0660
Ayrton BangoloHackensack Meridian School of Medicine, Nutley, NJ 07110, USA.ORCID 0000-0002-2133-2480
Parul JandirHackensack Meridian School of Medicine, Nutley, NJ 07110, USA.
Hong ZhangGenomic Testing Cooperative, Irvine, CA 92618, USA.
Sukhdeep KaurJohn Theurer Cancer Center, Hackensack, NJ 07601, USA.
Hyung C SuhJohn Theurer Cancer Center, Hackensack, NJ 07601, USA.ORCID 0000-0001-6912-4157
Michele DonatoJohn Theurer Cancer Center, Hackensack, NJ 07601, USA.
Maher AlbitarGenomic Testing Cooperative, Irvine, CA 92618, USA.
Andrew IpJohn Theurer Cancer Center, Hackensack, NJ 07601, USA.
Center for Discovery · USHackensack University Medical Center · USGenomic Health (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute graft-versus-host disease (aGvHD) remains a major cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation (HSCT). We performed RNA analysis of 1408 candidate genes in bone marrow samples obtained from 167 patients undergoing HSCT. RNA expression data were used in a machine learning algorithm to predict the presence or absence of aGvHD using either random forest or extreme gradient boosting algorithms. Patients were randomly divided into training (2/3 of patients) and validation (1/3 of patients) sets. Using post-HSCT RNA data, the machine learning algorithm selected 92 genes for predicting aGvHD that appear to play a role in PI3/AKT, MAPK, and FOXO signaling, as well as microRNA. The algorithm selected 20 genes for predicting survival included genes involved in MAPK and chemokine signaling. Using pre-HSCT RNA data, the machine learning algorithm selected 400 genes and 700 genes predicting aGvHD and overall survival, but candidate signaling pathways could not be specified in this analysis. These data show that NGS analyses of RNA expression using machine learning algorithms may be useful biomarkers of aGvHD and overall survival for patients undergoing HSCT, allowing for the identification of major signaling pathways associated with HSCT outcomes and helping to dissect the complex steps involved in the development of aGvHD. The analysis of pre-HSCT bone marrow samples may lead to pre-HSCT interventions including choice of remission induction regimens and modifications in patient health before HSCT.

Indexed as

acute GvHDallogeneic transplantationmachine learningpost-transplant survivalsignaling pathwaystranscriptomics

Identifiers

PMID38611035
PMCPMC11011125
OpenAlexW4393356612

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.