Cargando…

Mutational Profile of Metastatic Breast Cancer Tissue in Patients Treated with Exemestane Plus Everolimus

BACKGROUND: Everolimus has been shown to overcome endocrine resistance in hormone receptor positive advanced breast cancer patients. Predictive biomarkers of everolimus efficacy have been investigated in primary breast cancer tissue without finding univocal results. The goal of this study was to inv...

Descripción completa

Detalles Bibliográficos
Autores principales: Omarini, Claudia, Filieri, Maria Elisabetta, Bettelli, Stefania, Manfredini, Samantha, Kaleci, Shaniko, Caprera, Cecilia, Nasso, Cecilia, Barbolini, Monica, Guaitoli, Giorgia, Moscetti, Luca, Maiorana, Antonino, Conte, Pier Franco, Cascinu, Stefano, Piacentini, Federico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081542/
https://www.ncbi.nlm.nih.gov/pubmed/30140695
http://dx.doi.org/10.1155/2018/3756981
_version_ 1783345669077991424
author Omarini, Claudia
Filieri, Maria Elisabetta
Bettelli, Stefania
Manfredini, Samantha
Kaleci, Shaniko
Caprera, Cecilia
Nasso, Cecilia
Barbolini, Monica
Guaitoli, Giorgia
Moscetti, Luca
Maiorana, Antonino
Conte, Pier Franco
Cascinu, Stefano
Piacentini, Federico
author_facet Omarini, Claudia
Filieri, Maria Elisabetta
Bettelli, Stefania
Manfredini, Samantha
Kaleci, Shaniko
Caprera, Cecilia
Nasso, Cecilia
Barbolini, Monica
Guaitoli, Giorgia
Moscetti, Luca
Maiorana, Antonino
Conte, Pier Franco
Cascinu, Stefano
Piacentini, Federico
author_sort Omarini, Claudia
collection PubMed
description BACKGROUND: Everolimus has been shown to overcome endocrine resistance in hormone receptor positive advanced breast cancer patients. Predictive biomarkers of everolimus efficacy have been investigated in primary breast cancer tissue without finding univocal results. The goal of this study was to investigate the mutational burden in the metastatic site of endocrine-resistant tumors treated with everolimus plus exemestane. PATIENTS AND METHODS: Mass Array Sequenom platform was used to analyse genetic status of 18 cancer-related genes in 25 archival tumor specimens from metastatic lesions and available primary matched breast cancer tissue of patients treated with everolimus and exemestane for advanced disease. An exploratory analysis of everolimus efficacy in terms of progression free survival benefit and single gene mutation was carried out. RESULTS: The overall detection rate of mutation was 30% and 38% from metastatic and primary breast cancer samples, respectively. AKT1(E17K) was the most frequent mutated gene. No primary breast cancer and matched relapse maintained the same mutation profile. Considering molecular pathways, the most of the genes belong to PI3K pathway (AKT1(E17K), PI3KCA(E545K), and KIT(G565R,S709F)). In patients with detected mutations in breast and/or recurrence tissue the median PFS was 5,6 months while in the subgroup of patients with no mutations the median PFS was 7,5 months. CONCLUSIONS: The mutational status of breast cancer recurrence allows the identification of some genes potentially correlating tumor response/resistance to everolimus. The most frequently mutated genes were involved in the PI3K/AKT/mTOR pathway highlighting that the deregulation of this pathway in the relapse plays a crucial role in the mechanisms of everolimus resistance/sensitivity. Owing to the small sample size and the retrospective nature of the study, these correlations need to be validated in a large prospective study.
format Online
Article
Text
id pubmed-6081542
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-60815422018-08-23 Mutational Profile of Metastatic Breast Cancer Tissue in Patients Treated with Exemestane Plus Everolimus Omarini, Claudia Filieri, Maria Elisabetta Bettelli, Stefania Manfredini, Samantha Kaleci, Shaniko Caprera, Cecilia Nasso, Cecilia Barbolini, Monica Guaitoli, Giorgia Moscetti, Luca Maiorana, Antonino Conte, Pier Franco Cascinu, Stefano Piacentini, Federico Biomed Res Int Research Article BACKGROUND: Everolimus has been shown to overcome endocrine resistance in hormone receptor positive advanced breast cancer patients. Predictive biomarkers of everolimus efficacy have been investigated in primary breast cancer tissue without finding univocal results. The goal of this study was to investigate the mutational burden in the metastatic site of endocrine-resistant tumors treated with everolimus plus exemestane. PATIENTS AND METHODS: Mass Array Sequenom platform was used to analyse genetic status of 18 cancer-related genes in 25 archival tumor specimens from metastatic lesions and available primary matched breast cancer tissue of patients treated with everolimus and exemestane for advanced disease. An exploratory analysis of everolimus efficacy in terms of progression free survival benefit and single gene mutation was carried out. RESULTS: The overall detection rate of mutation was 30% and 38% from metastatic and primary breast cancer samples, respectively. AKT1(E17K) was the most frequent mutated gene. No primary breast cancer and matched relapse maintained the same mutation profile. Considering molecular pathways, the most of the genes belong to PI3K pathway (AKT1(E17K), PI3KCA(E545K), and KIT(G565R,S709F)). In patients with detected mutations in breast and/or recurrence tissue the median PFS was 5,6 months while in the subgroup of patients with no mutations the median PFS was 7,5 months. CONCLUSIONS: The mutational status of breast cancer recurrence allows the identification of some genes potentially correlating tumor response/resistance to everolimus. The most frequently mutated genes were involved in the PI3K/AKT/mTOR pathway highlighting that the deregulation of this pathway in the relapse plays a crucial role in the mechanisms of everolimus resistance/sensitivity. Owing to the small sample size and the retrospective nature of the study, these correlations need to be validated in a large prospective study. Hindawi 2018-07-24 /pmc/articles/PMC6081542/ /pubmed/30140695 http://dx.doi.org/10.1155/2018/3756981 Text en Copyright © 2018 Claudia Omarini et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Omarini, Claudia
Filieri, Maria Elisabetta
Bettelli, Stefania
Manfredini, Samantha
Kaleci, Shaniko
Caprera, Cecilia
Nasso, Cecilia
Barbolini, Monica
Guaitoli, Giorgia
Moscetti, Luca
Maiorana, Antonino
Conte, Pier Franco
Cascinu, Stefano
Piacentini, Federico
Mutational Profile of Metastatic Breast Cancer Tissue in Patients Treated with Exemestane Plus Everolimus
title Mutational Profile of Metastatic Breast Cancer Tissue in Patients Treated with Exemestane Plus Everolimus
title_full Mutational Profile of Metastatic Breast Cancer Tissue in Patients Treated with Exemestane Plus Everolimus
title_fullStr Mutational Profile of Metastatic Breast Cancer Tissue in Patients Treated with Exemestane Plus Everolimus
title_full_unstemmed Mutational Profile of Metastatic Breast Cancer Tissue in Patients Treated with Exemestane Plus Everolimus
title_short Mutational Profile of Metastatic Breast Cancer Tissue in Patients Treated with Exemestane Plus Everolimus
title_sort mutational profile of metastatic breast cancer tissue in patients treated with exemestane plus everolimus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081542/
https://www.ncbi.nlm.nih.gov/pubmed/30140695
http://dx.doi.org/10.1155/2018/3756981
work_keys_str_mv AT omariniclaudia mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus
AT filierimariaelisabetta mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus
AT bettellistefania mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus
AT manfredinisamantha mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus
AT kalecishaniko mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus
AT capreracecilia mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus
AT nassocecilia mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus
AT barbolinimonica mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus
AT guaitoligiorgia mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus
AT moscettiluca mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus
AT maioranaantonino mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus
AT contepierfranco mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus
AT cascinustefano mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus
AT piacentinifederico mutationalprofileofmetastaticbreastcancertissueinpatientstreatedwithexemestanepluseverolimus