Nomogram for the personalisation of radiotherapy treatments in breast cancer patients

Introduction: Numerous prospective studies have shown that the incorporation of genomic assays into clinical practice significantly impacts the choice of adjuvant treatments for patients with early-stage breast cancer. However, the same evidence does not exist for the treatment of locoregional recur...

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Autores principales: Inmaculada Beato Tortajada, Carlos Ferrer Albiach, Virginia Morillo Macias
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Lenguaje:EN
Publicado: Elsevier 2021
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spelling oai:doaj.org-article:34a937695973461ca48aa7a034ba64b62021-11-22T04:18:02ZNomogram for the personalisation of radiotherapy treatments in breast cancer patients1532-308010.1016/j.breast.2021.11.004https://doaj.org/article/34a937695973461ca48aa7a034ba64b62021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S0960977621009863https://doaj.org/toc/1532-3080Introduction: Numerous prospective studies have shown that the incorporation of genomic assays into clinical practice significantly impacts the choice of adjuvant treatments for patients with early-stage breast cancer. However, the same evidence does not exist for the treatment of locoregional recurrences. Hypothesis and objectives: The main objective of this work was to identify the clinicopathological, molecular, and genetic parameters that allow patients to be more precisely categorised into risk groups, in order to create a locoregional recurrence riskclassification tool, the PersonalRT27. Material and methods: To create PersonalRT27, we retrospective assessed the variables of patients with early breast cancer (stages I or II) who had undergone the OncotypeDx ® and MammaPrint ® genetic tests. These variables and factors included in the tests were categorised and weighted to obtain scores between 1 and 5 pointsto represent a lower or higher risk of relapse, respectively, based on these factors and as determined by the researchers. Results: The mean follow-up time was 60.5 months (range 25–96 months); locoregional progression-free survival at the time of the analysis was 98.4%, and overall survival was 97.5%, of which 0.6% of the deaths had been cancer specific. The area under the curve for the PersonalRT27 was 0.76 (95% CI [0.70, 0.81]), sensitivity was 78%, and the specificity was 58.9%. We used these factors to create an inhospital web-based nomogram. Conclusions: The PersonalRT27 is a novel tool that integrates clinical-pathological, molecular, and genetic parameters. External and independent validation will be required to implement its clinical use.Inmaculada Beato TortajadaCarlos Ferrer AlbiachVirginia Morillo MaciasElsevierarticleCáncer de mamaBreast cancerPlataformas genómicasGenetic assaysRecaída localLocal relapseNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENBreast, Vol 60, Iss , Pp 255-262 (2021)
institution DOAJ
collection DOAJ
language EN
topic Cáncer de mama
Breast cancer
Plataformas genómicas
Genetic assays
Recaída local
Local relapse
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle Cáncer de mama
Breast cancer
Plataformas genómicas
Genetic assays
Recaída local
Local relapse
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Inmaculada Beato Tortajada
Carlos Ferrer Albiach
Virginia Morillo Macias
Nomogram for the personalisation of radiotherapy treatments in breast cancer patients
description Introduction: Numerous prospective studies have shown that the incorporation of genomic assays into clinical practice significantly impacts the choice of adjuvant treatments for patients with early-stage breast cancer. However, the same evidence does not exist for the treatment of locoregional recurrences. Hypothesis and objectives: The main objective of this work was to identify the clinicopathological, molecular, and genetic parameters that allow patients to be more precisely categorised into risk groups, in order to create a locoregional recurrence riskclassification tool, the PersonalRT27. Material and methods: To create PersonalRT27, we retrospective assessed the variables of patients with early breast cancer (stages I or II) who had undergone the OncotypeDx ® and MammaPrint ® genetic tests. These variables and factors included in the tests were categorised and weighted to obtain scores between 1 and 5 pointsto represent a lower or higher risk of relapse, respectively, based on these factors and as determined by the researchers. Results: The mean follow-up time was 60.5 months (range 25–96 months); locoregional progression-free survival at the time of the analysis was 98.4%, and overall survival was 97.5%, of which 0.6% of the deaths had been cancer specific. The area under the curve for the PersonalRT27 was 0.76 (95% CI [0.70, 0.81]), sensitivity was 78%, and the specificity was 58.9%. We used these factors to create an inhospital web-based nomogram. Conclusions: The PersonalRT27 is a novel tool that integrates clinical-pathological, molecular, and genetic parameters. External and independent validation will be required to implement its clinical use.
format article
author Inmaculada Beato Tortajada
Carlos Ferrer Albiach
Virginia Morillo Macias
author_facet Inmaculada Beato Tortajada
Carlos Ferrer Albiach
Virginia Morillo Macias
author_sort Inmaculada Beato Tortajada
title Nomogram for the personalisation of radiotherapy treatments in breast cancer patients
title_short Nomogram for the personalisation of radiotherapy treatments in breast cancer patients
title_full Nomogram for the personalisation of radiotherapy treatments in breast cancer patients
title_fullStr Nomogram for the personalisation of radiotherapy treatments in breast cancer patients
title_full_unstemmed Nomogram for the personalisation of radiotherapy treatments in breast cancer patients
title_sort nomogram for the personalisation of radiotherapy treatments in breast cancer patients
publisher Elsevier
publishDate 2021
url https://doaj.org/article/34a937695973461ca48aa7a034ba64b6
work_keys_str_mv AT inmaculadabeatotortajada nomogramforthepersonalisationofradiotherapytreatmentsinbreastcancerpatients
AT carlosferreralbiach nomogramforthepersonalisationofradiotherapytreatmentsinbreastcancerpatients
AT virginiamorillomacias nomogramforthepersonalisationofradiotherapytreatmentsinbreastcancerpatients
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