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SABCS 2017 pathology: from bench to bedside

The 40th International San Antonio Breast Cancer Symposium offered a multifaceted platform for the presentation of several innovative therapeutic approaches. The results of these preclinical and clinical studies provided insight into the development of novel therapy concepts from the laboratory benc...

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Autor principal: Bago-Horvath, Zsuzsanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132829/
https://www.ncbi.nlm.nih.gov/pubmed/30220930
http://dx.doi.org/10.1007/s12254-018-0427-8
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author Bago-Horvath, Zsuzsanna
author_facet Bago-Horvath, Zsuzsanna
author_sort Bago-Horvath, Zsuzsanna
collection PubMed
description The 40th International San Antonio Breast Cancer Symposium offered a multifaceted platform for the presentation of several innovative therapeutic approaches. The results of these preclinical and clinical studies provided insight into the development of novel therapy concepts from the laboratory bench to the bedside of breast cancer patients. One main focus of last year’s symposium was the search for synergisms and opportunities for collaboration between basic research scientists and investigators in drug development. Highlights of these topics included preclinical data on selective estrogen receptor covalent antagonists (SERCAs), the discovery of immune-modulating effects of demethylating agents as well as the exact characterization and risk assessment of BRCA2 mutations of previously unknown significance. Pathological advances aimed at the molecular understanding of intratumoral heterogeneity and the evolution of lobular breast cancer. Beyond preclinical discoveries at the molecular level, clinical studies provided evidence on the duration of adjuvant bisphosphonate treatment and the use of the EndoPredict multigenomic assay to predict response to neoadjuvant chemo- and endocrine therapy. The SUCCESS A study reported that the prolonged adjuvant administration of zoledronic acid for 5 years did not improve patient survival after chemotherapy. A translational analysis of the ABCSG 34 trial revealed that the EndoPredict multigenomic assay could identify patients who do not benefit from neoadjuvant endocrine or chemotherapy. These recent advances are likely to promote individualized breast cancer care.
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spelling pubmed-61328292018-09-13 SABCS 2017 pathology: from bench to bedside Bago-Horvath, Zsuzsanna Memo Short Review The 40th International San Antonio Breast Cancer Symposium offered a multifaceted platform for the presentation of several innovative therapeutic approaches. The results of these preclinical and clinical studies provided insight into the development of novel therapy concepts from the laboratory bench to the bedside of breast cancer patients. One main focus of last year’s symposium was the search for synergisms and opportunities for collaboration between basic research scientists and investigators in drug development. Highlights of these topics included preclinical data on selective estrogen receptor covalent antagonists (SERCAs), the discovery of immune-modulating effects of demethylating agents as well as the exact characterization and risk assessment of BRCA2 mutations of previously unknown significance. Pathological advances aimed at the molecular understanding of intratumoral heterogeneity and the evolution of lobular breast cancer. Beyond preclinical discoveries at the molecular level, clinical studies provided evidence on the duration of adjuvant bisphosphonate treatment and the use of the EndoPredict multigenomic assay to predict response to neoadjuvant chemo- and endocrine therapy. The SUCCESS A study reported that the prolonged adjuvant administration of zoledronic acid for 5 years did not improve patient survival after chemotherapy. A translational analysis of the ABCSG 34 trial revealed that the EndoPredict multigenomic assay could identify patients who do not benefit from neoadjuvant endocrine or chemotherapy. These recent advances are likely to promote individualized breast cancer care. Springer Vienna 2018-08-15 2018 /pmc/articles/PMC6132829/ /pubmed/30220930 http://dx.doi.org/10.1007/s12254-018-0427-8 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Short Review
Bago-Horvath, Zsuzsanna
SABCS 2017 pathology: from bench to bedside
title SABCS 2017 pathology: from bench to bedside
title_full SABCS 2017 pathology: from bench to bedside
title_fullStr SABCS 2017 pathology: from bench to bedside
title_full_unstemmed SABCS 2017 pathology: from bench to bedside
title_short SABCS 2017 pathology: from bench to bedside
title_sort sabcs 2017 pathology: from bench to bedside
topic Short Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6132829/
https://www.ncbi.nlm.nih.gov/pubmed/30220930
http://dx.doi.org/10.1007/s12254-018-0427-8
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