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Multi-candidate immunohistochemical markers to assess radiation response and prognosis in prostate cancer: results from the CHHiP trial of radiotherapy fractionation

BACKGROUND: Protein markers of cellular proliferation, hypoxia, apoptosis, cell cycle checkpoints, growth factor signalling and inflammation in localised prostate tumours have previously shown prognostic ability. A translational substudy within the CHHiP trial of radiotherapy fractionation evaluated...

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Autores principales: Wilkins, Anna, Gusterson, Barry, Tovey, Holly, Griffin, Clare, Stuttle, Christine, Daley, Frances, Corbishley, Catherine M., Dearnaley, David, Hall, Emma, Somaiah, Navita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9900483/
https://www.ncbi.nlm.nih.gov/pubmed/36708693
http://dx.doi.org/10.1016/j.ebiom.2023.104436
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author Wilkins, Anna
Gusterson, Barry
Tovey, Holly
Griffin, Clare
Stuttle, Christine
Daley, Frances
Corbishley, Catherine M.
Dearnaley, David
Hall, Emma
Somaiah, Navita
author_facet Wilkins, Anna
Gusterson, Barry
Tovey, Holly
Griffin, Clare
Stuttle, Christine
Daley, Frances
Corbishley, Catherine M.
Dearnaley, David
Hall, Emma
Somaiah, Navita
author_sort Wilkins, Anna
collection PubMed
description BACKGROUND: Protein markers of cellular proliferation, hypoxia, apoptosis, cell cycle checkpoints, growth factor signalling and inflammation in localised prostate tumours have previously shown prognostic ability. A translational substudy within the CHHiP trial of radiotherapy fractionation evaluated whether these could improve prediction of prognosis and assist treatment stratification following either conventional or hypofractionated radiotherapy. METHODS: Using case:control methodology, patients with biochemical or clinical failure after radiotherapy (BCR) were matched to patients without recurrence according to established prognostic factors (Gleason score, presenting PSA, tumour-stage) and fractionation schedule. Immunohistochemical (IHC) staining of diagnostic biopsy sections was performed and scored for HIF1α, Bcl-2, Ki67, Geminin, p16, p53, p-chk1 and PTEN. Univariable and multivariable conditional logistic regression models, adjusted for matching strata and age, estimated the prognostic value of each IHC biomarker, including interaction terms to determine BCR prediction according to fractionation. FINDINGS: IHC results were available for up to 336 tumours. PTEN, Geminin, mean Ki67 and max Ki67 were prognostic after adjusting for multiple comparisons and were fitted in a multivariable model (n = 212, 106 matched pairs). Here, PTEN and Geminin showed significant prediction of prognosis. No marker predicted BCR according to fractionation. INTERPRETATION: Geminin or Ki67, and PTEN, predicted response to radiotherapy independently of established prognostic factors. These results provide essential independent external validation of previous findings and confirm a role for these markers in treatment stratification. FUNDING: 10.13039/501100000289Cancer Research UK (BIDD) grant (A12518), 10.13039/501100000289Cancer Research UK (C8262/A7253), Department of Health, 10.13039/501100000771Prostate Cancer UK, 10.13039/100008719Movember Foundation, NIHR Biomedical Research Centre at 10.13039/100012139Royal Marsden/ICR.
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spelling pubmed-99004832023-02-07 Multi-candidate immunohistochemical markers to assess radiation response and prognosis in prostate cancer: results from the CHHiP trial of radiotherapy fractionation Wilkins, Anna Gusterson, Barry Tovey, Holly Griffin, Clare Stuttle, Christine Daley, Frances Corbishley, Catherine M. Dearnaley, David Hall, Emma Somaiah, Navita eBioMedicine Articles BACKGROUND: Protein markers of cellular proliferation, hypoxia, apoptosis, cell cycle checkpoints, growth factor signalling and inflammation in localised prostate tumours have previously shown prognostic ability. A translational substudy within the CHHiP trial of radiotherapy fractionation evaluated whether these could improve prediction of prognosis and assist treatment stratification following either conventional or hypofractionated radiotherapy. METHODS: Using case:control methodology, patients with biochemical or clinical failure after radiotherapy (BCR) were matched to patients without recurrence according to established prognostic factors (Gleason score, presenting PSA, tumour-stage) and fractionation schedule. Immunohistochemical (IHC) staining of diagnostic biopsy sections was performed and scored for HIF1α, Bcl-2, Ki67, Geminin, p16, p53, p-chk1 and PTEN. Univariable and multivariable conditional logistic regression models, adjusted for matching strata and age, estimated the prognostic value of each IHC biomarker, including interaction terms to determine BCR prediction according to fractionation. FINDINGS: IHC results were available for up to 336 tumours. PTEN, Geminin, mean Ki67 and max Ki67 were prognostic after adjusting for multiple comparisons and were fitted in a multivariable model (n = 212, 106 matched pairs). Here, PTEN and Geminin showed significant prediction of prognosis. No marker predicted BCR according to fractionation. INTERPRETATION: Geminin or Ki67, and PTEN, predicted response to radiotherapy independently of established prognostic factors. These results provide essential independent external validation of previous findings and confirm a role for these markers in treatment stratification. FUNDING: 10.13039/501100000289Cancer Research UK (BIDD) grant (A12518), 10.13039/501100000289Cancer Research UK (C8262/A7253), Department of Health, 10.13039/501100000771Prostate Cancer UK, 10.13039/100008719Movember Foundation, NIHR Biomedical Research Centre at 10.13039/100012139Royal Marsden/ICR. Elsevier 2023-01-26 /pmc/articles/PMC9900483/ /pubmed/36708693 http://dx.doi.org/10.1016/j.ebiom.2023.104436 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Articles
Wilkins, Anna
Gusterson, Barry
Tovey, Holly
Griffin, Clare
Stuttle, Christine
Daley, Frances
Corbishley, Catherine M.
Dearnaley, David
Hall, Emma
Somaiah, Navita
Multi-candidate immunohistochemical markers to assess radiation response and prognosis in prostate cancer: results from the CHHiP trial of radiotherapy fractionation
title Multi-candidate immunohistochemical markers to assess radiation response and prognosis in prostate cancer: results from the CHHiP trial of radiotherapy fractionation
title_full Multi-candidate immunohistochemical markers to assess radiation response and prognosis in prostate cancer: results from the CHHiP trial of radiotherapy fractionation
title_fullStr Multi-candidate immunohistochemical markers to assess radiation response and prognosis in prostate cancer: results from the CHHiP trial of radiotherapy fractionation
title_full_unstemmed Multi-candidate immunohistochemical markers to assess radiation response and prognosis in prostate cancer: results from the CHHiP trial of radiotherapy fractionation
title_short Multi-candidate immunohistochemical markers to assess radiation response and prognosis in prostate cancer: results from the CHHiP trial of radiotherapy fractionation
title_sort multi-candidate immunohistochemical markers to assess radiation response and prognosis in prostate cancer: results from the chhip trial of radiotherapy fractionation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9900483/
https://www.ncbi.nlm.nih.gov/pubmed/36708693
http://dx.doi.org/10.1016/j.ebiom.2023.104436
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