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The Influence of Adjuvant Radiotherapy and Single Nucleotide Polymorphisms on Circulating Immune Response Cell Numbers and Phenotypes of Patients With Breast Cancer
Linköping University, Department of Clinical and Experimental Medicine, Division of Surgery, Orthopedics and Oncology. Linköping University, Faculty of Medicine and Health Sciences. Ryhov Hosp, Sweden.
Ryhov Hosp, Sweden; Naresuan Univ, Thailand.
Ryhov Hosp, Sweden.
Linköping University, Department of Clinical and Experimental Medicine, Division of Surgery, Orthopedics and Oncology. Linköping University, Faculty of Medicine and Health Sciences. Ryhov Hosp, Sweden.
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2019 (English)In: Anticancer Research, ISSN 0250-7005, E-ISSN 1791-7530, Vol. 39, no 9, p. 4957-4963Article in journal (Refereed) Published
Abstract [en]

Background/Aim: Adjuvant radiotherapy (RT) damages multiple layers of skin, muscle, blood vessels and blood cells that are included within the RT area. Indirect, bystander systemic effects could also develop in cells not directly hit by radiation. Materials and Methods: Ninety-three female patients recovering from breast cancer surgery and 82 female healthy blood donors were analyzed. For identification of systemic adaptive and innate immune response, rapid and low-cost blood-based biomarkers were assayed. Results: Post-operated breast cancer patients had a decreased number of circulating adaptive immune response cells but increased number of circulating immunosuppressive myeloid subpopulations. RT decreased the number of T-cells and platelets without influencing the number of immunosuppressive myeloid subpopulations. Alterations in the number and phenotypes of T-cell subpopulations were associated with SNPs. Conclusion: The combination of RT and immunotherapy might provide optimal treatment for cancer patients.

Place, publisher, year, edition, pages
INT INST ANTICANCER RESEARCH , 2019. Vol. 39, no 9, p. 4957-4963
Keywords [en]
Breast cancer; radiotherapy; blood-based biomarkers
National Category
Cancer and Oncology
Identifiers
URN: urn:nbn:se:liu:diva-161187DOI: 10.21873/anticanres.13684ISI: 000486457600047PubMedID: 31519601OAI: oai:DiVA.org:liu-161187DiVA, id: diva2:1365696
Note

Funding Agencies|Jonkoping Clinical Cancer Research Foundation [110426-1]; Futurum [144631]; FORSS [567001]; Thai Office of Science and Technology in Brussels, Ministry of Science and Technology

Available from: 2019-10-25 Created: 2019-10-25 Last updated: 2019-10-25

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Lewin, NongnitOliva, DelmyAndersson, Bengt-Åke
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