Evidence map›Paper›PMID 37163491›Full record

ArticlePloS one2023

Monitoring plasma nucleosome concentrations to measure disease response and progression in dogs with hematopoietic malignancies.

Heather Wilson-Robles, Emma Warry, Tasha Miller, Jill Jarvis, Matthew Matsushita, Pamela Miller, Marielle Herzog, Jean-Valery Turatsinze, Theresa K Kelly, S Thomas Butera and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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

11 authors at 3 institutions in 2 countries.

Heather Wilson-RoblesSmall Animal Clinical Sciences Department, Texas A&M University, College Station, Texas, United States of America.ORCID 0000-0002-6489-8468
Emma WarrySmall Animal Clinical Sciences Department, Texas A&M University, College Station, Texas, United States of America.
Tasha MillerSmall Animal Clinical Sciences Department, Texas A&M University, College Station, Texas, United States of America.
Jill JarvisSmall Animal Clinical Sciences Department, Texas A&M University, College Station, Texas, United States of America.
Matthew MatsushitaSmall Animal Clinical Sciences Department, Texas A&M University, College Station, Texas, United States of America.
Pamela MillerSmall Animal Clinical Sciences Department, Texas A&M University, College Station, Texas, United States of America.
Marielle HerzogBelgian Volition SRL, Parc Scientifique Crealys, Isnes, Belgium.
Jean-Valery TuratsinzeBelgian Volition SRL, Parc Scientifique Crealys, Isnes, Belgium.
Theresa K KellyVolition America LLC, Henderson, Nevada, United States of America.
S Thomas ButeraVolition Veterinary Diagnostics Development, Henderson, Nevada, United States of America.
Gaetan MichelBelgian Volition SRL, Parc Scientifique Crealys, Isnes, Belgium.
Texas A&M University · USVolition (United States) · USVolition (Belgium) · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHematopoietic malignancies are extremely common in pet dogs and represent nearly 30% of the malignancies diagnosed in this population each year. Clinicians commonly use existing tools such as physical exam findings, radiographs, ultrasound and baseline blood work to monitor these patients for treatment response and remission. Circulating biomarkers, such as prostate specific antigen or carcinoembryonic antigen, can be useful tools for monitoring treatment response and remission status in human cancer patients. To date, there has a been a lack of useful circulating biomarkers available to veterinary oncology patients.

methodsCirculating plasma nucleosome concentrations were evaluated at diagnosis, throughout treatment and during remission monitoring for 40 dogs with lymphoma, acute myelogenous leukemia and multiple myeloma. Additionally, C-reactive protein and thymidine kinase-1 levels were recorded.

resultsPlasma nucleosome concentrations were significantly higher at diagnosis and progressive disease than they were when dogs were in remission. All but two dogs had plasma nucleosome concentrations that returned to the low range during treatment. These two dogs had the shortest progression free and overall survival times. Dogs with the highest plasma nucleosome concentrations had a significantly shorter first progression free survival than dogs with lower plasma nucleosome concentrations at diagnosis. Plasma nucleosome concentrations correlated better with disease response and progression than either thymidine kinase or C reactive protein.

conclusionsPlasma nucleosome concentrations can be a useful tool for treatment monitoring and disease progression in dogs with hematopoietic malignancies.

Indexed as

Dog DiseasesHematologic NeoplasmsNeoplasmsAnimalsBiomarkersC-Reactive ProteinDogsHumansMaleNucleosomesThymidine KinaseBiomarkersC-Reactive ProteinNucleosomesThymidine Kinase

Identifiers

PMID37163491
PMCPMC10171669
OpenAlexW4376133485

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.