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Tumour Infiltrating Lymphocytes (TILs) and immune composition in breast cancer patients from Kenya: Spatial distributions and associations with risk factors and tumour characteristics.
Sayed, Shahin; Koka, Hela; Abubakar, Mustapha; Gardner, Kevin; Salgado, Roberto; Moloo, Zahir; Caban-Ureña, Ambar Beatriz; Rosen, Daniel; Castro, Patricia; Saleh, Mansoor; Shaikh, Asim Jamal; Shah, Jasmit; Figueroa, Jonine; Makokha, Francis; Ha, Hien Khanh; Wang, Zhong; Magangane, Pumza; Naidoo, Richard; Ngundo, Veronica; Yang, Xiaohong Rose; Govender, Dhirendra.
Affiliation
  • Sayed S; Department of Pathology, Aga Khan University, East Africa, P.O Box30270- 00100, Nairobi, Kenya. shaheen.sayed@aku.edu.
  • Koka H; Division of Anatomical Pathology, University of Cape Town, Cape Town, South Africa. shaheen.sayed@aku.edu.
  • Abubakar M; Integrative Tumour Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Gardner K; Integrative Tumour Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Salgado R; Department of Pathology and Cell Biology, Columbia University Medical Center, Columbia University, New York, NY, USA.
  • Moloo Z; Department of Pathology/Division of Research, Peter MacCallum Cancer, Melbourne, VIC, 3000, Australia.
  • Caban-Ureña AB; Department of Pathology, GZA-ZNA Hospitals, Wilrijk, Antwerp, Belgium.
  • Rosen D; Department of Pathology, ZAS Hospitals, Antwerp, Belgium.
  • Castro P; Department of Pathology, Aga Khan University, East Africa, P.O Box30270- 00100, Nairobi, Kenya.
  • Saleh M; Department of Pathology and Cell Biology, Columbia University Medical Center, Columbia University, New York, NY, USA.
  • Shaikh AJ; Department of Pathology & Immunology, Baylor College of Medicine, Houston, USA.
  • Shah J; Department of Pathology & Immunology, Baylor College of Medicine, Houston, USA.
  • Figueroa J; Department of Pathology, Aga Khan University, East Africa, P.O Box30270- 00100, Nairobi, Kenya.
  • Makokha F; Department of Pathology, Aga Khan University, East Africa, P.O Box30270- 00100, Nairobi, Kenya.
  • Ha HK; Comprehensive Cancer Care and Research, Sultan Qaboos Comprehensive Cancer Care and Research Institute, Muscat, Oman.
  • Wang Z; Department of Pathology, Aga Khan University, East Africa, P.O Box30270- 00100, Nairobi, Kenya.
  • Magangane P; The Usher Institute and CRUK Edinburgh Cancer Centre, The University of Edinburgh, Edinburgh, Scotland.
  • Naidoo R; Department of Human Health Research Programme, Mount Kenya University, Thika, Kenya.
  • Ngundo V; Department of Biochemistry, University of Alberta, Edmonton, Canada.
  • Yang XR; Department of Pathology and Cell Biology, Columbia University Medical Center, Columbia University, New York, NY, USA.
  • Govender D; Department of Pathology, University of Witwatersrand, Johannesburg, South Africa.
Breast Cancer Res Treat ; 199(2): 401-413, 2023 Jun.
Article in En | MEDLINE | ID: mdl-37010652
BACKGROUND: The 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. METHODS: Visual 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. RESULTS: A 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. CONCLUSION: The 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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms Type of study: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limits: Female / Humans Country/Region as subject: Africa Language: En Journal: Breast Cancer Res Treat Year: 2023 Type: Article Affiliation country: Kenya

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms Type of study: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Limits: Female / Humans Country/Region as subject: Africa Language: En Journal: Breast Cancer Res Treat Year: 2023 Type: Article Affiliation country: Kenya