Evidence map›Paper›PMID 37628721›Full record

ArticleInternational journal of molecular sciences2023

Low Pretreatment CD4

Ross J Turner, Thomas V Guy, Nicholas J Geraghty, Ashleigh Splitt, Debbie Watson, Daniel Brungs, Martin G Carolan, Andrew A Miller, Jeremiah F de Leon, Morteza Aghmesheh and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. 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 4 institutions in 1 country.

Ross J TurnerMolecular Horizons and School of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, NSW 2522, Australia.
Thomas V GuyIllawarra Health and Medical Research Institute, Wollongong, NSW 2522, Australia.
Nicholas J GeraghtyMolecular Horizons and School of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, NSW 2522, Australia.ORCID 0000-0001-9098-8224
Ashleigh SplittIllawarra Cancer Care Centre, Wollongong Hospital, Wollongong, NSW 2500, Australia.ORCID 0000-0002-2085-8034
Debbie WatsonMolecular Horizons and School of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, NSW 2522, Australia.
Daniel BrungsIllawarra Cancer Care Centre, Wollongong Hospital, Wollongong, NSW 2500, Australia.
Martin G CarolanIllawarra Cancer Care Centre, Wollongong Hospital, Wollongong, NSW 2500, Australia.
Andrew A MillerIllawarra Cancer Care Centre, Wollongong Hospital, Wollongong, NSW 2500, Australia.
Jeremiah F de LeonGenesisCare, St Vincent's Clinic, Darlinghurst, NSW 2010, Australia.
Morteza AghmeshehIllawarra Cancer Care Centre, Wollongong Hospital, Wollongong, NSW 2500, Australia.
Ronald SluyterMolecular Horizons and School of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, NSW 2522, Australia.ORCID 0000-0003-4909-686X
University of Wollongong · AUWollongong Hospital · AUIllawarra Health and Medical Research Institute · AUSt Vincent's Clinic · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ectonucleotidases CD39 and CD73 are present on immune cells and play important roles in cancer progression by suppressing antitumour immunity. As such, CD39 and CD73 on peripheral blood mononuclear cells (PBMCs) are emerging as potential biomarkers to predict disease outcomes and treatment responses in cancer patients. This study aimed to examine T and B cells, including CD39 and CD73 expressing subsets, by flow cytometry in PBMCs from 28 patients with head and neck squamous cell carcinoma (HNSCC) and to assess the correlation with the treatment modality, human papillomavirus (HPV) status, and relapse-free survival (RFS). The PBMCs were examined pre-, mid-, and post-radiotherapy with concurrent cisplatin chemotherapy or anti-epidermal growth factor receptor antibody (cetuximab) therapy. Combination radiotherapy caused changes to T and B cell populations, including CD39 and CD73 expressing subsets, but no such differences were observed between concurrent chemotherapy and cetuximab. Pretreatment PBMCs from HPV

Indexed as

Head and Neck NeoplasmsPapillomavirus InfectionsAdaptor Proteins, Signal TransducingAntigens, CD19CD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCetuximabChronic DiseaseHumansLeukocytes, MononuclearNeoplasm Recurrence, LocalSquamous Cell Carcinoma of Head and NeckAdaptor Proteins, Signal TransducingAntigens, CD19CetuximabENTPD1head and neck cancerhuman papillomaviruslymphocyteNT5E

Identifiers

PMID37628721
PMCPMC10454544
OpenAlexW4385899161

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.