Evidence map›Paper›PMID 32580514›Full record

ReviewCells2020

Intratumoral Versus Circulating Lymphoid Cells as Predictive Biomarkers in Lung Cancer Patients Treated with Immune Checkpoint Inhibitors: Is the Easiest Path the Best One?

Marta Gascón, Dolores Isla, Mara Cruellas, Eva M Gálvez, Rodrigo Lastra, Maitane Ocáriz, José Ramón Paño, Ariel Ramírez, Andrea Sesma, Irene Torres-Ramón and 3 more

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
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  11. Cell Therapy with Human Reprogrammed CD8International journal of molecular sciences · 2022
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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

13 authors at 4 institutions in 1 country.

Marta GascónMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.ORCID 0000-0002-6811-6654
Dolores IslaMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.
Mara CruellasMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.
Eva M GálvezCarbochemical Institute (ICB-CSIC), Miguel Luesma 4, 50018 Zaragoza, Spain.ORCID 0000-0001-6928-5516
Rodrigo LastraMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.
Maitane OcárizMedical Oncology Department, University Hospital Lozano Blesa, 50009 Zaragoza, Spain.
José Ramón PañoAragon Health Research Institute (IIS Aragón) 50009 Zaragoza, Spain.
Ariel RamírezNanotoxicology and Immunotoxicology Unit (IIS Aragón), 50009 Zaragoza, Spain.
Andrea SesmaMedical 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.
Julián PardoAragon Health Research Institute (IIS Aragón) 50009 Zaragoza, Spain.
Luis Martínez-LostaoAragon Health Research Institute (IIS Aragón) 50009 Zaragoza, Spain.
Hospital Clínico Universitario Lozano Blesa · ESUniversidad de Zaragoza · ESInstituto de Carboquímica · ESInstituto de Investigación Sanitaria Aragón · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The molecular and cell determinants that modulate immune checkpoint (ICI) efficacy in lung cancer are still not well understood. However, there is a necessity to select those patients that will most benefit from these new treatments. Recent studies suggest the presence and/or the relative balance of specific lymphoid cells in the tumor microenvironment (TEM) including the T cell (activated, memory, and regulatory) and NK cell (CD56dim/bright) subsets, and correlate with a better response to ICI. The analyses of these cell subsets in peripheral blood, as a more accessible and homogeneous sample, might facilitate clinical decisions concerning fast prediction of ICI efficacy. Despite recent studies suggesting that lymphoid circulating cells might correlate with ICI efficacy and toxicity, more analyses and investigation are required to confirm if circulating lymphoid cells are a relevant picture of the lung TME and could be instrumental as ICI response biomarkers. This short review is aimed to discuss the recent advances in this fast-growing field.

Indexed as

Biomarkers, TumorHumansImmune Checkpoint InhibitorsLung NeoplasmsLymphocytesTumor MicroenvironmentBiomarkers, TumorImmune Checkpoint Inhibitorsbiomarkersimmune cells in cancerimmune checkpoints inhibitorslung cancertumor microenvironment

Identifiers

PMID32580514
PMCPMC7348938
OpenAlexW3036393236

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.