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Multiomic Characterization of High-Grade Serous Ovarian Carcinoma Enables High-Resolution Patient Stratification

PURPOSE: High-grade serous ovarian carcinoma (HGSOC) is the most common ovarian cancer type; most patients experience disease recurrence that accumulates chemoresistance, leading to treatment failure. Genomic and transcriptomic features have been associated with differential outcome and treatment re...

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Autores principales: Hollis, Robert L., Meynert, Alison M., Michie, Caroline O., Rye, Tzyvia, Churchman, Michael, Hallas-Potts, Amelia, Croy, Ian, McCluggage, W. Glenn, Williams, Alistair R.W., Bartos, Clare, Iida, Yasushi, Okamoto, Aikou, Dougherty, Brian, Barrett, J. Carl, March, Ruth, Matakidou, Athena, Roxburgh, Patricia, Semple, Colin A., Harkin, D. Paul, Kennedy, Richard, Herrington, C. Simon, Gourley, Charlie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for Cancer Research 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9662902/
https://www.ncbi.nlm.nih.gov/pubmed/35696721
http://dx.doi.org/10.1158/1078-0432.CCR-22-0368
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author Hollis, Robert L.
Meynert, Alison M.
Michie, Caroline O.
Rye, Tzyvia
Churchman, Michael
Hallas-Potts, Amelia
Croy, Ian
McCluggage, W. Glenn
Williams, Alistair R.W.
Bartos, Clare
Iida, Yasushi
Okamoto, Aikou
Dougherty, Brian
Barrett, J. Carl
March, Ruth
Matakidou, Athena
Roxburgh, Patricia
Semple, Colin A.
Harkin, D. Paul
Kennedy, Richard
Herrington, C. Simon
Gourley, Charlie
author_facet Hollis, Robert L.
Meynert, Alison M.
Michie, Caroline O.
Rye, Tzyvia
Churchman, Michael
Hallas-Potts, Amelia
Croy, Ian
McCluggage, W. Glenn
Williams, Alistair R.W.
Bartos, Clare
Iida, Yasushi
Okamoto, Aikou
Dougherty, Brian
Barrett, J. Carl
March, Ruth
Matakidou, Athena
Roxburgh, Patricia
Semple, Colin A.
Harkin, D. Paul
Kennedy, Richard
Herrington, C. Simon
Gourley, Charlie
author_sort Hollis, Robert L.
collection PubMed
description PURPOSE: High-grade serous ovarian carcinoma (HGSOC) is the most common ovarian cancer type; most patients experience disease recurrence that accumulates chemoresistance, leading to treatment failure. Genomic and transcriptomic features have been associated with differential outcome and treatment response. However, the relationship between events at the gene sequence, copy number, and gene-expression levels remains poorly defined. EXPERIMENTAL DESIGN: We perform multiomic characterization of a large HGSOC cohort (n = 362) with detailed clinical annotation to interrogate the relationship between patient subgroups defined by specific molecular events. RESULTS: BRCA2-mutant (BRCA2m) and EMSY-overexpressing cases demonstrated prolonged survival [multivariable hazard ratios (HR) 0.40 and 0.51] and significantly higher first- and second-line chemotherapy response rate. CCNE1-gained (CCNE1g) cases demonstrated underrepresentation of FIGO stage IV cases, with shorter survival but no significant difference in treatment response. We demonstrate marked overlap between the TCGA- and Tothill-derived subtypes. IMR/C2 cases displayed higher BRCA1/2m frequency (25.5%, 32.5%) and significantly greater immune cell infiltration, whereas PRO/C5 cases had the highest CCNE1g rate (23.9%, 22.2%) and were uniformly low in immune cell infiltration. The survival benefit for cases with aberrations in homologous recombination repair (HRR) genes was apparent across all transcriptomic subtypes (HR range, 0.48–0.68). There was significant co-occurrence of RB loss and HRR gene aberrations; RB loss was further associated with favorable survival within HRR-aberrant cases (multivariable HR, 0.50). CONCLUSIONS: These data paint a high-resolution picture of the molecular landscape in HGSOC, better defining patients who may benefit most from specific molecular therapeutics and highlighting those for whom novel treatment strategies are needed to improve outcomes.
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spelling pubmed-96629022023-01-05 Multiomic Characterization of High-Grade Serous Ovarian Carcinoma Enables High-Resolution Patient Stratification Hollis, Robert L. Meynert, Alison M. Michie, Caroline O. Rye, Tzyvia Churchman, Michael Hallas-Potts, Amelia Croy, Ian McCluggage, W. Glenn Williams, Alistair R.W. Bartos, Clare Iida, Yasushi Okamoto, Aikou Dougherty, Brian Barrett, J. Carl March, Ruth Matakidou, Athena Roxburgh, Patricia Semple, Colin A. Harkin, D. Paul Kennedy, Richard Herrington, C. Simon Gourley, Charlie Clin Cancer Res Precision Medicine and Imaging PURPOSE: High-grade serous ovarian carcinoma (HGSOC) is the most common ovarian cancer type; most patients experience disease recurrence that accumulates chemoresistance, leading to treatment failure. Genomic and transcriptomic features have been associated with differential outcome and treatment response. However, the relationship between events at the gene sequence, copy number, and gene-expression levels remains poorly defined. EXPERIMENTAL DESIGN: We perform multiomic characterization of a large HGSOC cohort (n = 362) with detailed clinical annotation to interrogate the relationship between patient subgroups defined by specific molecular events. RESULTS: BRCA2-mutant (BRCA2m) and EMSY-overexpressing cases demonstrated prolonged survival [multivariable hazard ratios (HR) 0.40 and 0.51] and significantly higher first- and second-line chemotherapy response rate. CCNE1-gained (CCNE1g) cases demonstrated underrepresentation of FIGO stage IV cases, with shorter survival but no significant difference in treatment response. We demonstrate marked overlap between the TCGA- and Tothill-derived subtypes. IMR/C2 cases displayed higher BRCA1/2m frequency (25.5%, 32.5%) and significantly greater immune cell infiltration, whereas PRO/C5 cases had the highest CCNE1g rate (23.9%, 22.2%) and were uniformly low in immune cell infiltration. The survival benefit for cases with aberrations in homologous recombination repair (HRR) genes was apparent across all transcriptomic subtypes (HR range, 0.48–0.68). There was significant co-occurrence of RB loss and HRR gene aberrations; RB loss was further associated with favorable survival within HRR-aberrant cases (multivariable HR, 0.50). CONCLUSIONS: These data paint a high-resolution picture of the molecular landscape in HGSOC, better defining patients who may benefit most from specific molecular therapeutics and highlighting those for whom novel treatment strategies are needed to improve outcomes. American Association for Cancer Research 2022-08-15 2022-06-13 /pmc/articles/PMC9662902/ /pubmed/35696721 http://dx.doi.org/10.1158/1078-0432.CCR-22-0368 Text en ©2022 The Authors; Published by the American Association for Cancer Research https://creativecommons.org/licenses/by/4.0/This open access article is distributed under the Creative Commons Attribution 4.0 International (CC BY 4.0) license.
spellingShingle Precision Medicine and Imaging
Hollis, Robert L.
Meynert, Alison M.
Michie, Caroline O.
Rye, Tzyvia
Churchman, Michael
Hallas-Potts, Amelia
Croy, Ian
McCluggage, W. Glenn
Williams, Alistair R.W.
Bartos, Clare
Iida, Yasushi
Okamoto, Aikou
Dougherty, Brian
Barrett, J. Carl
March, Ruth
Matakidou, Athena
Roxburgh, Patricia
Semple, Colin A.
Harkin, D. Paul
Kennedy, Richard
Herrington, C. Simon
Gourley, Charlie
Multiomic Characterization of High-Grade Serous Ovarian Carcinoma Enables High-Resolution Patient Stratification
title Multiomic Characterization of High-Grade Serous Ovarian Carcinoma Enables High-Resolution Patient Stratification
title_full Multiomic Characterization of High-Grade Serous Ovarian Carcinoma Enables High-Resolution Patient Stratification
title_fullStr Multiomic Characterization of High-Grade Serous Ovarian Carcinoma Enables High-Resolution Patient Stratification
title_full_unstemmed Multiomic Characterization of High-Grade Serous Ovarian Carcinoma Enables High-Resolution Patient Stratification
title_short Multiomic Characterization of High-Grade Serous Ovarian Carcinoma Enables High-Resolution Patient Stratification
title_sort multiomic characterization of high-grade serous ovarian carcinoma enables high-resolution patient stratification
topic Precision Medicine and Imaging
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9662902/
https://www.ncbi.nlm.nih.gov/pubmed/35696721
http://dx.doi.org/10.1158/1078-0432.CCR-22-0368
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