Evidence map›Paper›PMID 35716311›Full record

ArticleJournal of neuro-oncology2022

Pre-surgery immune profiles of adult glioma patients.

Paige M Bracci, Terri Rice, Helen M Hansen, Stephen S Francis, Sean Lee, Lucie S McCoy, Pavan P Shrestha, Gayathri Warrier, Jennifer L Clarke, Annette M Molinaro and 3 more

Abstract read
In one paragraph

Article in Journal of neuro-oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. 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

13 authors.

Paige M BracciDepartment of Epidemiology and Biostatistics, UCSF, 1450 3rd Street, San Francisco, CA, 94158, USA. paige.bracci@ucsf.edu.
Terri RiceDepartment of Neurological Surgery, UCSF, San Francisco, CA, USA.
Helen M HansenDepartment of Neurological Surgery, UCSF, San Francisco, CA, USA.
Stephen S FrancisDepartment of Neurological Surgery, UCSF, San Francisco, CA, USA.
Sean LeeDepartment of Neurological Surgery, UCSF, San Francisco, CA, USA.
Lucie S McCoyDepartment of Neurological Surgery, UCSF, San Francisco, CA, USA.
Pavan P ShresthaDepartment of Neurological Surgery, UCSF, San Francisco, CA, USA.
Gayathri WarrierDepartment of Neurological Surgery, UCSF, San Francisco, CA, USA.
Jennifer L ClarkeDepartment of Neurological Surgery, UCSF, San Francisco, CA, USA.
Annette M MolinaroDepartment of Epidemiology and Biostatistics, UCSF, 1450 3rd Street, San Francisco, CA, 94158, USA.
Jennie W TaylorDepartment of Neurological Surgery, UCSF, San Francisco, CA, USA.
John K WienckeDepartment of Neurological Surgery, UCSF, San Francisco, CA, USA.
Margaret R WrenschDepartment of Neurological Surgery, UCSF, San Francisco, CA, USA.

Funding

UCSF CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR024131 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JOHNSTON, S. CLAIBORNE · 2006 to 2011
$111.2M
Tissue CoreP50CA097257 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Joseph F Costello · 2002 to 2026
$57.4M
Immune epigenetic biomarkers of survival in glioma epidemiologyR01CA207360 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WIENCKE, JOHN K. · 2017 to 2021
$3.8M
NCI NIH HHS P50 CA097257NCI NIH HHS R01 CA207360NCRR NIH HHS UL1 RR024131NIH HHS P50CA097257NIH HHS R01CA207360
6 · The paper itself

Abstract

introductionAlthough immunosuppression is a known characteristic of glioma, no previous large studies have reported peripheral blood immune cell profiles prior to patient surgery and chemoradiation. This report describes blood immune cell characteristics and associated variables prior to surgery among typical glioma patients seen at a large University practice.

methodsWe analyzed pre-surgery blood samples from 139 glioma patients diagnosed with a new or recurrent grade II/III glioma (LrGG, n = 64) or new glioblastoma (GBM, n = 75) and 454 control participants without glioma. Relative cell fractions of CD4, CD8, B-cells, Natural Killer cells, monocytes, and neutrophils, were estimated via a validated deconvolution algorithm from blood DNA methylation measures from Illumina EPIC arrays.

resultsDexamethasone use at time of blood draw varied by glioma type being highest among patients with IDH wild-type (wt) GBM (75%) and lowest for those with oligodendroglioma (14%). Compared to controls, glioma patients showed statistically significant lower cell fractions for all immune cell subsets except for neutrophils which were higher (all p-values < 0.001), in part because of the higher prevalence of dexamethasone use at time of blood draw for IDHwt GBM. Patients who were taking dexamethasone were more likely to have a low CD4 count (< 200, < 500), increased neutrophils, low absolute lymphocyte counts, higher total cell count and higher NLR.

conclusionWe show that pre-surgery blood immune profiles vary by glioma subtype, age, and more critically, by use of dexamethasone. Our results highlight the importance of considering dexamethasone exposures in all studies of immune profiles and of obtaining immune measures prior to use of dexamethasone, if possible.

Indexed as

Brain NeoplasmsGlioblastomaGliomaAdultDexamethasoneHumansIsocitrate DehydrogenaseNeoplasm Recurrence, LocalDexamethasoneIsocitrate DehydrogenaseDeconvolution methodsDexamethasoneGlioblastomaImmune cell subsetLower grade gliomaMethylation

Identifiers

PMID35716311
PMCPMC9325836

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.