Evidence map›Paper›PMID 36612271›Full record

ArticleCancers2022

Tumor Microenvironment before and after Chemoradiation in Locally Advanced Rectal Cancer: Beyond PD-L1.

Pritam Tayshetye, Andrew J Friday, Ashten N Omstead, Tanvi Verma, Stacey Miller, Ping Zheng, Prashant Jani, Ali Zaidi, Gene Finley

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Observational
  10. Article
  11. Review
  12. Review
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

9 authors at 3 institutions in 2 countries.

Pritam TayshetyeDepartment of Hematology-Oncology, Allegheny Health Network, Pittsburgh, PA 15212, USA.ORCID 0000-0003-2635-8863
Andrew J FridayDepartment of Medical Oncology, Allegheny General Hospital, Pittsburgh, PA 15212, USA.
Ashten N OmsteadEsophageal and Lung Institute, Allegheny Health Network, Pittsburgh, PA 15212, USA.
Tanvi VermaDepartment of Pathology and Laboratory Medicine, Allegheny Health Network, Pittsburgh, PA 15212, USA.
Stacey MillerDepartment of Pathology and Laboratory Medicine, Allegheny Health Network, Pittsburgh, PA 15212, USA.
Ping ZhengEsophageal and Lung Institute, Allegheny Health Network, Pittsburgh, PA 15212, USA.
Prashant JaniHematology and Oncology, Northeast Cancer Centre, Sudbury, ON P3E 5J1, Canada.
Ali ZaidiEsophageal and Lung Institute, Allegheny Health Network, Pittsburgh, PA 15212, USA.
Gene FinleyDepartment of Medical Oncology, Allegheny General Hospital, Pittsburgh, PA 15212, USA.
Allegheny Health Network · USAllegheny General Hospital · USNortheast Cancer Centre · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn locally advanced rectal cancer treatment, neoadjuvant concurrent chemoradiation therapy (cCRT) is the standard of care. The tumor microenvironment (TME) is a complex entity comprising of tumor cells, immune cells and surrounding stroma and is closely associated with tumor growth and survival, response to antitumor therapies and also resistance to treatment. We aimed to assess the change in biomarkers associated with TME following standard neoadjuvant cCRT in rectal cancer.

methodsWe accessed archival tissue from rectal cancer patients treated with neoadjuvant cCRT at Allegheny Health Network (AHN) facilities over the past 14 years. Pre-treatment and post-treatment biopsies were assayed for PD-L1, CD8+ T-cells, CXCL9, TIM-3, IDO-1, IFN-G, IL17RE, LAG-3, and OX40 in 41 patients.

resultsWe found statistically significant upregulation in multiple biomarkers namely CD8, IL17RE, LAG3 and OX40 post neoadjuvant cCRT and a trend towards upregulation, although not statistically significant, in biomarkers PD-L1, CXCL9, TIM-3, IDO-1 and IFN-G expression.

conclusionsThis provides a glimpse into the TME before and after neoadjuvant cCRT. We suggest that the biomarkers noted to be upregulated could be used for designing appropriate clinical trials and development of therapeutic targeted drug therapy in an effort to achieve better response to neoadjuvant therapy, increasing clinical and pathological complete response rates and improved overall outcomes.

Indexed as

biomarkerchemoradiationimmunotherapyneoadjuvantrectal cancertumor microenvironment

Identifiers

PMID36612271
PMCPMC9818440
OpenAlexW4313389229

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.