Evidence map›Paper›PMID 37010652›Full record

ArticleBreast cancer research and treatment2023

Tumour Infiltrating Lymphocytes (TILs) and immune composition in breast cancer patients from Kenya: Spatial distributions and associations with risk factors and tumour characteristics.

Shahin Sayed, Hela Koka, Mustapha Abubakar, Kevin Gardner, Roberto Salgado, Zahir Moloo, Ambar Beatriz Caban-Ureña, Daniel Rosen, Patricia Castro, Mansoor Saleh and 11 more

Open access · greenAbstract read
In one paragraph

Article in Breast cancer research and treatment, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 4 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

21 authors at 10 institutions in 7 countries.

Shahin Sayed *Department of Pathology, Aga Khan University, East Africa, P.O Box30270- 00100, Nairobi, Kenya. shaheen.sayed@aku.edu.ORCID http://orcid.org/0000-0002-3472-511X
Hela KokaIntegrative Tumour Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Mustapha AbubakarIntegrative Tumour Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Kevin GardnerDepartment of Pathology and Cell Biology, Columbia University Medical Center, Columbia University, New York, NY, USA.
Roberto SalgadoDepartment of Pathology/Division of Research, Peter MacCallum Cancer, Melbourne, VIC, 3000, Australia.
Zahir MolooDepartment of Pathology, Aga Khan University, East Africa, P.O Box30270- 00100, Nairobi, Kenya.
Ambar Beatriz Caban-UreñaDepartment of Pathology and Cell Biology, Columbia University Medical Center, Columbia University, New York, NY, USA.
Daniel RosenDepartment of Pathology & Immunology, Baylor College of Medicine, Houston, USA.
Patricia CastroDepartment of Pathology & Immunology, Baylor College of Medicine, Houston, USA.
Mansoor SalehDepartment of Pathology, Aga Khan University, East Africa, P.O Box30270- 00100, Nairobi, Kenya.
Asim Jamal ShaikhDepartment of Pathology, Aga Khan University, East Africa, P.O Box30270- 00100, Nairobi, Kenya.
Jasmit ShahDepartment of Pathology, Aga Khan University, East Africa, P.O Box30270- 00100, Nairobi, Kenya.
Jonine FigueroaThe Usher Institute and CRUK Edinburgh Cancer Centre, The University of Edinburgh, Edinburgh, Scotland.
Francis MakokhaDepartment of Human Health Research Programme, Mount Kenya University, Thika, Kenya.
Hien Khanh HaDepartment of Biochemistry, University of Alberta, Edmonton, Canada.
Zhong WangDepartment of Pathology and Cell Biology, Columbia University Medical Center, Columbia University, New York, NY, USA.
Pumza MaganganeDepartment of Pathology, University of Witwatersrand, Johannesburg, South Africa.
Richard NaidooDivision of Anatomical Pathology, University of Cape Town, Cape Town, South Africa.
Veronica NgundoDepartment of Pathology, Aga Khan University, East Africa, P.O Box30270- 00100, Nairobi, Kenya.
Xiaohong Rose Yang *Integrative Tumour Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Dhirendra Govender *Division of Anatomical Pathology, University of Cape Town, Cape Town, South Africa.
Aga Khan University Nairobi · KEColumbia University Irving Medical Center · USNational Institutes of Health · USUniversity of Cape Town · ZABaylor College of Medicine · USEdinburgh Cancer Research · GBMount Kenya University · KEPeter MacCallum Cancer Centre · AUUniversity of Alberta · CAUniversity of the Witwatersrand · ZA

Funding

Hormone-Related CancersZIACP010126 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI GIERACH, GRETCHEN · 2009 to 2025
$103.5M
Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
The linkage between Race, Kaiso and the tumor microenvironment in breast cancer health disparitiesR01CA253368 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GARDNER, KEVIN L. · 2020 to 2024
$3.3M
The Role of Kaiso as a predictive breast cancer biomarker in Africa and across the African DiasporaR01CA266040 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KEVIN L. GARDNER · 2022 to 2026
$3.1M
Medical Research Council MR/S015027/1NCI NIH HHS P30 CA125123NCI NIH HHS R01 CA253368NCI NIH HHS R01 CA266040
6 · The paper itself

Abstract

backgroundThe immune landscape of breast cancer (BC) in patients from Sub Saharan Africa is understudied. Our aims were to describe the distribution of Tumour Infiltrating Lymphocytes (TILs) within the intratumoural stroma (sTILs) and the leading/invasive edge stroma (LE-TILs), and to evaluate TILs across BC subtypes with established risk factors and clinical characteristics in Kenyan women.

methodsVisual quantification of sTILs and LE-TILs were performed on Haematoxylin and eosin -stained pathologically confirmed BC cases based on the International TIL working group guidelines. Tissue Microarrays were constructed and stained with immunohistochemistry (IHC) for CD3, CD4, CD8, CD68, CD20, and FOXP3. Linear and logistic regression models were used to assess associations between risk factors and tumour features with IHC markers and total TILs, after adjusting for other covariates.

resultsA total of 226 invasive BC cases were included. Overall, LE-TIL (mean = 27.9, SD = 24.5) proportions were significantly higher than sTIL (mean = 13.5, SD = 15.8). Both sTILs and LE- TILs were predominantly composed of CD3, CD8, and CD68. We found higher TILs to be associated with high KI67/high grade and aggressive tumour subtypes, although these associations varied by TIL locations. Older age at menarche (≥ 15 vs. < 15 years) was associated with higher CD3 (OR: 2.06, 95%CI:1.26-3.37), but only for the intra-tumour stroma.

conclusionThe TIL enrichment in more aggressive BCs is similar to previously published data in other populations. The distinct associations of sTIL/LE-TIL measures with most examined factors highlight the importance of spatial TIL evaluations in future studies.

Indexed as

Breast NeoplasmsFemaleHumansKenyaLymphocytes, Tumor-InfiltratingPrognosisBreast cancerImmune compositionSpatial distributionTIL distributionTumour characteristicsTumour Infiltrating Lymphocytes (TIL)

Identifiers

PMID37010652
PMCPMC11568797
OpenAlexW4362506944

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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.