Evidence map›Paper›PMID 39083705›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2024

Evaluation of CD3 and CD8 T-Cell Immunohistochemistry for Prognostication and Prediction of Benefit From Adjuvant Chemotherapy in Early-Stage Colorectal Cancer Within the QUASAR Trial.

Christopher J M Williams, Richard Gray, Robert K Hills, Michael Shires, Liping Zhang, Zuo Zhao, Tracie Gardner, Nancy Sapanara, Xiao-Meng Xu, Isaac Bai and 15 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2024. 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
–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

17 citing papers in PubMed.

  1. Systemic inflammation and prognosis in patients with RAS/BRAF wild-type metastatic colorectal cancer receiving anti-EGFR therapy: A real-world cohort study.Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland · 2026
    Article
  2. Article
  3. CD8Cancer science · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Immunoscore based on CD3American journal of cancer research · 2026
    Article
  8. Review
  9. Article
  10. Article
  11. CD103Clinical and translational medicine · 2025
    Article
  12. Article
  13. Review
  14. Review
  15. Intratumoural CD8Cancer immunology, immunotherapy : CII · 2024
    Article
  16. Review
  17. 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

25 authors.

Christopher J M WilliamsDivision of Pathology and Data Analytics, University of Leeds, Leeds, United Kingdom.ORCID 0000-0002-1574-653X
Richard GrayNuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-4440-574X
Robert K HillsNuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
Michael ShiresDivision of Pathology and Data Analytics, University of Leeds, Leeds, United Kingdom.ORCID 0000-0003-0904-6200
Liping ZhangRoche Diagnostics Solutions, Clinical Development and Medical Affairs, Oro Valley, AZ.ORCID 0009-0006-7739-4396
Zuo ZhaoRoche Diagnostics Solutions, Imaging and Algorithms, Digital Pathology, Santa Clara, CA.
Tracie GardnerRoche Diagnostics Solutions, Clinical Development and Medical Affairs, Oro Valley, AZ.
Nancy SapanaraRoche Diagnostics Solutions, Clinical Development and Medical Affairs, Oro Valley, AZ.
Xiao-Meng XuRoche Diagnostics Solutions, Clinical Development and Medical Affairs, Oro Valley, AZ.
Isaac BaiRoche Diagnostics Solutions, Clinical Development and Medical Affairs, Oro Valley, AZ.
Dongyao YanRoche Diagnostics Solutions, Clinical Development and Medical Affairs, Oro Valley, AZ.ORCID 0009-0001-9482-3539
Andrea MuranyiRoche Diagnostics Solutions, Research and Development, Oro Valley, AZ.
Sarah DanceRoche Diagnostics Limited, Medical Affairs, Burgess Hill, West Sussex, United Kingdom.
Faranak AghaeiRoche Diagnostics Solutions, Imaging and Algorithms, Digital Pathology, Santa Clara, CA.
Gemma HemmingsDivision of Pathology and Data Analytics, University of Leeds, Leeds, United Kingdom.
Michael HaleDivision of Pathology and Data Analytics, University of Leeds, Leeds, United Kingdom.ORCID 0000-0001-8178-6882
Uday KurkureRoche Diagnostics Solutions, Imaging and Algorithms, Digital Pathology, Santa Clara, CA.
Christoph GuetterRoche Diagnostics Solutions, Imaging and Algorithms, Digital Pathology, Santa Clara, CA.
Susan D RichmanDivision of Pathology and Data Analytics, University of Leeds, Leeds, United Kingdom.ORCID 0000-0003-3993-5041
Gordon HutchinsDivision of Pathology and Data Analytics, University of Leeds, Leeds, United Kingdom.
Jenny F SeligmannLeeds Institute of Medical Research, University of Leeds, Leeds, United Kingdom.ORCID 0000-0003-4379-6005
Nicholas P WestDivision of Pathology and Data Analytics, University of Leeds, Leeds, United Kingdom.ORCID 0000-0002-0346-6709
Shalini SinghRoche Diagnostics Solutions, Clinical Development and Medical Affairs, Oro Valley, AZ.
Kandavel ShanmugamRoche Diagnostics Solutions, Clinical Development and Medical Affairs, Oro Valley, AZ.ORCID 0000-0002-9076-3444
Philip QuirkeDivision of Pathology and Data Analytics, University of Leeds, Leeds, United Kingdom.ORCID 0000-0002-3597-5444

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeHigh densities of tumor infiltrating CD3 and CD8 T-cells are associated with superior prognosis in colorectal cancer (CRC). Their value as predictors of benefit from adjuvant chemotherapy is uncertain. PATIENTS AND

methodsTumor tissue from 868 patients in the QUASAR trial (adjuvant fluorouracil/folinic acid

resultsIn the training set, the recurrence rate in the high-risk group was twice that in the low-risk group for all measures (CD3-CT: rate ratio [RR], 2.00,

conclusionRecurrence rates in the high-risk CD3/CD8 groups are twice those in the low-risk groups. Proportional reductions with chemotherapy are similar, allowing NNTs derived in QUASAR to be updated using contemporary, nonrandomized data sets.

Indexed as

CD3 ComplexCD8-Positive T-LymphocytesColorectal NeoplasmsFluorouracilImmunohistochemistryAdultAgedAntineoplastic Combined Chemotherapy ProtocolsCD8 AntigensChemotherapy, AdjuvantFemaleHumansLeucovorinLymphocytes, Tumor-InfiltratingMaleMiddle AgedCD3 ComplexCD8 AntigensFluorouracilLeucovorin

Identifiers

PMID39083705
PMCPMC11458110

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.