Show simple item record

dc.contributor.authorMachiels, M
dc.contributor.authorOulkadi, R
dc.contributor.authorTramm, T
dc.contributor.authorStecklein, SR
dc.contributor.authorSomaiah, N
dc.contributor.authorDe Caluwé, A
dc.contributor.authorKlein, J
dc.contributor.authorTran, WT
dc.contributor.authorSalgado, R
dc.date.accessioned2023-07-19T08:47:34Z
dc.date.available2023-07-19T08:47:34Z
dc.date.issued2023-10-01
dc.identifier.citationThe Breast, 2023, 71 pp. 13 - 21
dc.identifier.issn0960-9776
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5894
dc.identifier.doi10.1016/j.breast.2023.06.010
dc.description.abstractRadiation therapy (RT) has long been fundamental for the curative treatment of breast cancer. While substantial progress has been made in the anatomical and technological precision of RT delivery, and some approaches to de-escalate or omit RT based on clinicopathologic features have been successful, there remain substantial opportunities to refine individualised RT based on tumour biology. A major area of clinical and research interest is to ascertain the individualised risk of loco-regional recurrence to direct treatment decisions regarding escalation and de-escalation of RT. Patient-tailored treatment with RT is considerably lagging behind compared with the massive progress made in the field of personalised medicine that currently mainly applies to decisions on the use of systemic therapy or targeted agents. Herein we review select literature surrounding the use of tumour genomic biomarkers and biomarkers of the immune system, including tumour infiltrating lymphocytes (TILs), within the management of breast cancer, specifically as they relate to progress in moving toward analytically validated and clinically tested biomarkers utilized in RT.
dc.format.extent13 - 21
dc.languageen
dc.language.isoeng
dc.publisherCHURCHILL LIVINGSTONE
dc.relation.ispartofThe Breast
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleIndividualising radiation therapy decisions in breast cancer patients based on tumour infiltrating lymphocytes and genomic biomarkers.
dc.typeJournal Article
dcterms.dateAccepted2023-06-27
dc.date.updated2023-07-19T08:46:03Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1016/j.breast.2023.06.010
rioxxterms.licenseref.startdate2023-10-01
rioxxterms.typeJournal Article/Review
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Translational Breast Radiobiology
pubs.publication-statusAccepted
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.breast.2023.06.010
pubs.volume71
icr.researchteamTrans Breast Radiobiol
dc.contributor.icrauthorSomaiah, Navita
icr.provenanceDeposited by Mr Arek Surman (impersonating Dr Navita Somaiah) on 2023-07-19. Deposit type is initial. No. of files: 1. Files: PIIS0960977623005143.pdf


Files in this item

Thumbnail

This item appears in the following collection(s)

Show simple item record

https://creativecommons.org/licenses/by-nc-nd/4.0/
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc-nd/4.0/