Evidence map›Paper›PMID 36672279›Full record

ArticleCancers2023

A Subset of PD-1-Expressing CD56

Marta Gascón-Ruiz, Ariel Ramírez-Labrada, Rodrigo Lastra, Luis Martínez-Lostao, J Ramón Paño-Pardo, Andrea Sesma, María Zapata-García, Alba Moratiel, Elisa Quílez, Irene Torres-Ramón and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

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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

16 authors at 5 institutions in 1 country.

Marta Gascón-RuizMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.ORCID 0000-0002-6811-6654
Ariel Ramírez-LabradaNanotoxicology and Immunotoxicology Unit (IIS Aragón), 50009 Zaragoza, Spain.ORCID 0000-0002-3888-7036
Rodrigo LastraMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.
Luis Martínez-LostaoAragon Health Research Institute (IIS Aragón), 50009 Zaragoza, Spain.
J Ramón Paño-PardoAragon Health Research Institute (IIS Aragón), 50009 Zaragoza, Spain.
Andrea SesmaMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.ORCID 0000-0001-7209-266X
María Zapata-GarcíaMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.ORCID 0000-0001-6654-8106
Alba MoratielMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.
Elisa QuílezMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.
Irene Torres-RamónMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.
Alfonso YuberoMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.
María Pilar DomingoInstituto de Carboquímica (ICB-CSIC), Miguel Luesma 4, 50018 Zaragoza, Spain.ORCID 0000-0002-6829-8769
Patricia EstebanAragon Health Research Institute (IIS Aragón), 50009 Zaragoza, Spain.ORCID 0000-0003-4123-3524
Eva M GálvezCIBER de Enfermedades Infecciosas (CIBERINFEC), 28029 Madrid, Spain.ORCID 0000-0001-6928-5516
Julián PardoAragon Health Research Institute (IIS Aragón), 50009 Zaragoza, Spain.ORCID 0000-0003-0154-0730
Dolores IslaMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.ORCID 0000-0002-2483-198X
Hospital Clínico Universitario Lozano Blesa · ESCentro de Investigación Biomédica en Red · ESUniversidad de Zaragoza · ESInstituto de Carboquímica · ESInstituto de Investigación Sanitaria Aragón · ES

Funding

AspanoaBristol Myers SquibbCarrera de la mujer de MonzónFondo europeo de desarrollo regional, Gobierno de Aragón Group B29_20RInstituto de Salud Carlos IIIMICIN/AEI PID2020- 113963RBI00Roche Farma S.A
6 · The paper itself

Abstract

(1) Despite the effectiveness of immune checkpoint inhibitors (ICIs) in lung cancer, there is a lack of knowledge about predictive biomarkers. The objective of our study is to analyze different subsets of T-lymphocytes and natural killer (NK) cells as predictive biomarkers in a cohort of patients with nonsmall cell lung cancer (NSCLC) treated with ICI. (2) This is an observational, prospective study with 55 NSCLC patients treated with ICI. A total of 43 T and NK cell subsets are analyzed in peripheral blood, including the main markers of exhaustion, differentiation, memory, activation, and inhibition. (3) Regarding the descriptive data, Granzyme B+CD4+ Treg lymphocytes stand out (median 17.4%), and within the NK populations, most patients presented cytotoxic NK cells (CD56+CD3-CD16+GranzymeB+; median 94.8%), and about half of them have highly differentiated adaptive-like NK cells (CD56+CD3-CD16+CD57+ (mean 59.8%). A statistically significant difference was observed between the expression of PD1 within the CD56

Indexed as

biomarkersimmunotherapylung cancerNK cellsT lymphocytes

Identifiers

PMID36672279
PMCPMC9856517
OpenAlexW4313588467

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.