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Validation analysis of the novel imaging-based prognostic radiomic signature in patients undergoing primary surgery for advanced high-grade serous ovarian cancer (HGSOC)

BACKGROUND: Predictive models based on radiomics features are novel, highly promising approaches for gynaecological oncology. Here, we wish to assess the prognostic value of the newly discovered Radiomic Prognostic Vector (RPV) in an independent cohort of high-grade serous ovarian cancer (HGSOC) pat...

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Autores principales: Fotopoulou, Christina, Rockall, Andrea, Lu, Haonan, Lee, Philippa, Avesani, Giacomo, Russo, Luca, Petta, Federica, Ataseven, Beyhan, Waltering, Kai-Uwe, Koch, Jens Albrecht, Crum, William R., Cunnea, Paula, Heitz, Florian, Harter, Philipp, Aboagye, Eric O., du Bois, Andreas, Prader, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8979975/
https://www.ncbi.nlm.nih.gov/pubmed/34923575
http://dx.doi.org/10.1038/s41416-021-01662-w
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author Fotopoulou, Christina
Rockall, Andrea
Lu, Haonan
Lee, Philippa
Avesani, Giacomo
Russo, Luca
Petta, Federica
Ataseven, Beyhan
Waltering, Kai-Uwe
Koch, Jens Albrecht
Crum, William R.
Cunnea, Paula
Heitz, Florian
Harter, Philipp
Aboagye, Eric O.
du Bois, Andreas
Prader, Sonia
author_facet Fotopoulou, Christina
Rockall, Andrea
Lu, Haonan
Lee, Philippa
Avesani, Giacomo
Russo, Luca
Petta, Federica
Ataseven, Beyhan
Waltering, Kai-Uwe
Koch, Jens Albrecht
Crum, William R.
Cunnea, Paula
Heitz, Florian
Harter, Philipp
Aboagye, Eric O.
du Bois, Andreas
Prader, Sonia
author_sort Fotopoulou, Christina
collection PubMed
description BACKGROUND: Predictive models based on radiomics features are novel, highly promising approaches for gynaecological oncology. Here, we wish to assess the prognostic value of the newly discovered Radiomic Prognostic Vector (RPV) in an independent cohort of high-grade serous ovarian cancer (HGSOC) patients, treated within a Centre of Excellence, thus avoiding any bias in treatment quality. METHODS: RPV was calculated using standardised algorithms following segmentation of routine preoperative imaging of patients (n = 323) who underwent upfront debulking surgery (01/2011-07/2018). RPV was correlated with operability, survival and adjusted for well-established prognostic factors (age, postoperative residual disease, stage), and compared to previous validation models. RESULTS: The distribution of low, medium and high RPV scores was 54.2% (n = 175), 33.4% (n = 108) and 12.4% (n = 40) across the cohort, respectively. High RPV scores independently associated with significantly worse progression-free survival (PFS) (HR = 1.69; 95% CI:1.06–2.71; P = 0.038), even after adjusting for stage, age, performance status and residual disease. Moreover, lower RPV was significantly associated with total macroscopic tumour clearance (OR = 2.02; 95% CI:1.56–2.62; P = 0.00647). CONCLUSIONS: RPV was validated to independently identify those HGSOC patients who will not be operated tumour-free in an optimal setting, and those who will relapse early despite complete tumour clearance upfront. Further prospective, multicentre trials with a translational aspect are warranted for the incorporation of this radiomics approach into clinical routine.
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spelling pubmed-89799752022-04-20 Validation analysis of the novel imaging-based prognostic radiomic signature in patients undergoing primary surgery for advanced high-grade serous ovarian cancer (HGSOC) Fotopoulou, Christina Rockall, Andrea Lu, Haonan Lee, Philippa Avesani, Giacomo Russo, Luca Petta, Federica Ataseven, Beyhan Waltering, Kai-Uwe Koch, Jens Albrecht Crum, William R. Cunnea, Paula Heitz, Florian Harter, Philipp Aboagye, Eric O. du Bois, Andreas Prader, Sonia Br J Cancer Article BACKGROUND: Predictive models based on radiomics features are novel, highly promising approaches for gynaecological oncology. Here, we wish to assess the prognostic value of the newly discovered Radiomic Prognostic Vector (RPV) in an independent cohort of high-grade serous ovarian cancer (HGSOC) patients, treated within a Centre of Excellence, thus avoiding any bias in treatment quality. METHODS: RPV was calculated using standardised algorithms following segmentation of routine preoperative imaging of patients (n = 323) who underwent upfront debulking surgery (01/2011-07/2018). RPV was correlated with operability, survival and adjusted for well-established prognostic factors (age, postoperative residual disease, stage), and compared to previous validation models. RESULTS: The distribution of low, medium and high RPV scores was 54.2% (n = 175), 33.4% (n = 108) and 12.4% (n = 40) across the cohort, respectively. High RPV scores independently associated with significantly worse progression-free survival (PFS) (HR = 1.69; 95% CI:1.06–2.71; P = 0.038), even after adjusting for stage, age, performance status and residual disease. Moreover, lower RPV was significantly associated with total macroscopic tumour clearance (OR = 2.02; 95% CI:1.56–2.62; P = 0.00647). CONCLUSIONS: RPV was validated to independently identify those HGSOC patients who will not be operated tumour-free in an optimal setting, and those who will relapse early despite complete tumour clearance upfront. Further prospective, multicentre trials with a translational aspect are warranted for the incorporation of this radiomics approach into clinical routine. Nature Publishing Group UK 2021-12-18 2022-04-01 /pmc/articles/PMC8979975/ /pubmed/34923575 http://dx.doi.org/10.1038/s41416-021-01662-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Fotopoulou, Christina
Rockall, Andrea
Lu, Haonan
Lee, Philippa
Avesani, Giacomo
Russo, Luca
Petta, Federica
Ataseven, Beyhan
Waltering, Kai-Uwe
Koch, Jens Albrecht
Crum, William R.
Cunnea, Paula
Heitz, Florian
Harter, Philipp
Aboagye, Eric O.
du Bois, Andreas
Prader, Sonia
Validation analysis of the novel imaging-based prognostic radiomic signature in patients undergoing primary surgery for advanced high-grade serous ovarian cancer (HGSOC)
title Validation analysis of the novel imaging-based prognostic radiomic signature in patients undergoing primary surgery for advanced high-grade serous ovarian cancer (HGSOC)
title_full Validation analysis of the novel imaging-based prognostic radiomic signature in patients undergoing primary surgery for advanced high-grade serous ovarian cancer (HGSOC)
title_fullStr Validation analysis of the novel imaging-based prognostic radiomic signature in patients undergoing primary surgery for advanced high-grade serous ovarian cancer (HGSOC)
title_full_unstemmed Validation analysis of the novel imaging-based prognostic radiomic signature in patients undergoing primary surgery for advanced high-grade serous ovarian cancer (HGSOC)
title_short Validation analysis of the novel imaging-based prognostic radiomic signature in patients undergoing primary surgery for advanced high-grade serous ovarian cancer (HGSOC)
title_sort validation analysis of the novel imaging-based prognostic radiomic signature in patients undergoing primary surgery for advanced high-grade serous ovarian cancer (hgsoc)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8979975/
https://www.ncbi.nlm.nih.gov/pubmed/34923575
http://dx.doi.org/10.1038/s41416-021-01662-w
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