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Differences in Tumour Aggressiveness Based on Molecular Subtype and Race Measured by [(18)F]FDG PET Metabolic Metrics in Patients with Invasive Carcinoma of the Breast

Breast cancer in women of African descent tends to be more aggressive with poorer prognosis. This is irrespective of the molecular subtype. [(18)F]FDG PET/CT metrics correlate with breast cancer aggressiveness based on molecular subtype. This study investigated the differences in [(18)F]FDG PET/CT m...

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Autores principales: Abubakar, Sofiullah, More, Stuart, Tag, Naima, Olabinjo, Afusat, Isah, Ahmed, Lawal, Ismaheel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297178/
https://www.ncbi.nlm.nih.gov/pubmed/37370954
http://dx.doi.org/10.3390/diagnostics13122059
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author Abubakar, Sofiullah
More, Stuart
Tag, Naima
Olabinjo, Afusat
Isah, Ahmed
Lawal, Ismaheel
author_facet Abubakar, Sofiullah
More, Stuart
Tag, Naima
Olabinjo, Afusat
Isah, Ahmed
Lawal, Ismaheel
author_sort Abubakar, Sofiullah
collection PubMed
description Breast cancer in women of African descent tends to be more aggressive with poorer prognosis. This is irrespective of the molecular subtype. [(18)F]FDG PET/CT metrics correlate with breast cancer aggressiveness based on molecular subtype. This study investigated the differences in [(18)F]FDG PET/CT metrics of locally advanced invasive ductal carcinoma (IDC) among different racial groups and molecular subtypes. Qualitative and semiquantitative readings of [(18)F]FDG PET/CT acquired in women with locally advanced IDC were performed. Biodata including self-identified racial grouping and histopathological data of the primary breast cancer were retrieved. Statistical analysis for differences in SUVmax, MTV and TLG of the primary tumour and the presence of regional and distant metastases was conducted based on molecular subtype and race. The primary tumour SUVmax, MTV, TLG and the prevalence of distant metastases were significantly higher in Black patients compared with other races (p < 0.05). The primary tumour SUVmax and presence of distant metastases in the luminal subtype and the primary tumour SUVmax and TLG in the basal subtype were significantly higher in Black patients compared with other races (p < 0.05). The significantly higher PET parameters in Black patients with IDC in general and in those with luminal and basal carcinoma subtypes suggest a more aggressive disease phenotype in this race.
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spelling pubmed-102971782023-06-28 Differences in Tumour Aggressiveness Based on Molecular Subtype and Race Measured by [(18)F]FDG PET Metabolic Metrics in Patients with Invasive Carcinoma of the Breast Abubakar, Sofiullah More, Stuart Tag, Naima Olabinjo, Afusat Isah, Ahmed Lawal, Ismaheel Diagnostics (Basel) Article Breast cancer in women of African descent tends to be more aggressive with poorer prognosis. This is irrespective of the molecular subtype. [(18)F]FDG PET/CT metrics correlate with breast cancer aggressiveness based on molecular subtype. This study investigated the differences in [(18)F]FDG PET/CT metrics of locally advanced invasive ductal carcinoma (IDC) among different racial groups and molecular subtypes. Qualitative and semiquantitative readings of [(18)F]FDG PET/CT acquired in women with locally advanced IDC were performed. Biodata including self-identified racial grouping and histopathological data of the primary breast cancer were retrieved. Statistical analysis for differences in SUVmax, MTV and TLG of the primary tumour and the presence of regional and distant metastases was conducted based on molecular subtype and race. The primary tumour SUVmax, MTV, TLG and the prevalence of distant metastases were significantly higher in Black patients compared with other races (p < 0.05). The primary tumour SUVmax and presence of distant metastases in the luminal subtype and the primary tumour SUVmax and TLG in the basal subtype were significantly higher in Black patients compared with other races (p < 0.05). The significantly higher PET parameters in Black patients with IDC in general and in those with luminal and basal carcinoma subtypes suggest a more aggressive disease phenotype in this race. MDPI 2023-06-14 /pmc/articles/PMC10297178/ /pubmed/37370954 http://dx.doi.org/10.3390/diagnostics13122059 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Abubakar, Sofiullah
More, Stuart
Tag, Naima
Olabinjo, Afusat
Isah, Ahmed
Lawal, Ismaheel
Differences in Tumour Aggressiveness Based on Molecular Subtype and Race Measured by [(18)F]FDG PET Metabolic Metrics in Patients with Invasive Carcinoma of the Breast
title Differences in Tumour Aggressiveness Based on Molecular Subtype and Race Measured by [(18)F]FDG PET Metabolic Metrics in Patients with Invasive Carcinoma of the Breast
title_full Differences in Tumour Aggressiveness Based on Molecular Subtype and Race Measured by [(18)F]FDG PET Metabolic Metrics in Patients with Invasive Carcinoma of the Breast
title_fullStr Differences in Tumour Aggressiveness Based on Molecular Subtype and Race Measured by [(18)F]FDG PET Metabolic Metrics in Patients with Invasive Carcinoma of the Breast
title_full_unstemmed Differences in Tumour Aggressiveness Based on Molecular Subtype and Race Measured by [(18)F]FDG PET Metabolic Metrics in Patients with Invasive Carcinoma of the Breast
title_short Differences in Tumour Aggressiveness Based on Molecular Subtype and Race Measured by [(18)F]FDG PET Metabolic Metrics in Patients with Invasive Carcinoma of the Breast
title_sort differences in tumour aggressiveness based on molecular subtype and race measured by [(18)f]fdg pet metabolic metrics in patients with invasive carcinoma of the breast
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297178/
https://www.ncbi.nlm.nih.gov/pubmed/37370954
http://dx.doi.org/10.3390/diagnostics13122059
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