Evidence map›Paper›PMID 33753562›Full record

ReviewJournal of clinical pathology2021

Tumour immune microenvironment biomarkers predicting cytotoxic chemotherapy efficacy in colorectal cancer.

Kate Wilkinson, Weng Ng, Tara Laurine Roberts, Therese M Becker, Stephanie Hui-Su Lim, Wei Chua, Cheok Soon Lee

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of clinical pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

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  19. Systemic Interleukins' Profile in Early and Advanced Colorectal Cancer.International journal of molecular sciences · 2021
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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

7 authors at 3 institutions in 1 country.

Kate WilkinsonLiverpool Cancer Therapy Centre, Liverpool Hospital, Liverpool, New South Wales, Australia kate.wilkinson1@health.nsw.gov.au.ORCID http://orcid.org/0000-0001-8318-4615
Weng NgLiverpool Cancer Therapy Centre, Liverpool Hospital, Liverpool, New South Wales, Australia.
Tara Laurine RobertsSchool of Medicine, Western Sydney University, Liverpool, New South Wales, Australia.
Therese M BeckerSchool of Medicine, Western Sydney University, Liverpool, New South Wales, Australia.
Stephanie Hui-Su LimSchool of Medicine, Western Sydney University, Liverpool, New South Wales, Australia.
Wei ChuaLiverpool Cancer Therapy Centre, Liverpool Hospital, Liverpool, New South Wales, Australia.
Cheok Soon LeeSchool of Medicine, Western Sydney University, Liverpool, New South Wales, Australia.
Liverpool Hospital · AUIngham Institute · AUCamden and Campbelltown Hospitals · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of the local tumour and stromal immune landscape is increasingly recognised to be important in cancer development, progression and response to therapy. The composition, function, spatial orientation and gene expression profile of the infiltrate of the innate and adaptive immune system at the tumour and surrounding tissue has an established prognostic role in colorectal cancer (CRC). Multiple studies have confirmed that a tumour immune microenvironment (TIME) reflective of a type 1 adaptive immune response is associated with improved prognosis. There have been significant efforts to evolve these observations into validated, histopathology-based prognostic biomarkers, such as the Immunoscore. However, the clinical need lies much more in the development of predictive, not prognostic, biomarkers which have the potential to improve patient outcomes. This is particularly pertinent to help guide cytotoxic chemotherapy use in CRC, which remains the standard of care. Cytotoxic chemotherapy has recognised immunomodulatory activity distinct from its antimitotic effects, including mechanisms such as immunogenic cell death (ICD) and induction/inhibition of key immune players. Response to chemotherapy may differ with regard to molecular subtype of CRC, which are strongly associated with immune phenotypes. Thus, immune markers are potentially useful, though under-reported, predictive biomarkers. In this review, we discuss the impact of the TIME on response to cytotoxic chemotherapy in CRC, with a focus on baseline immune markers, and associated genomic and transcriptomic signatures.

Indexed as

Antineoplastic AgentsBiomarkers, TumorColorectal NeoplasmsDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansImmune Checkpoint ProteinsInflammation MediatorsLymphocytes, Tumor-InfiltratingTreatment OutcomeTumor-Associated MacrophagesTumor MicroenvironmentAntineoplastic AgentsBiomarkers, TumorImmune Checkpoint ProteinsInflammation Mediatorsbiomarkerscolorectal neoplasmsimmunohistochemistrylymphocytesstromal cellstumour

Identifiers

PMID33753562
PMCPMC8461409
OpenAlexW3136949094

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.