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The C Allele of ATM rs11212617 Associates With Higher Pathological Complete Remission Rate in Breast Cancer Patients Treated With Neoadjuvant Metformin.

Authors :
Cuyàs E
Buxó M
Ferri Iglesias MJ
Verdura S
Pernas S
Dorca J
Álvarez I
Martínez S
Pérez-Garcia JM
Batista-López N
Rodríguez-Sánchez CA
Amillano K
Domínguez S
Luque M
Morilla I
Stradella A
Viñas G
Cortés J
Joven J
Brunet J
López-Bonet E
Garcia M
Saidani S
Queralt Moles X
Martin-Castillo B
Menendez JA
Source :
Frontiers in oncology [Front Oncol] 2019 Mar 28; Vol. 9, pp. 193. Date of Electronic Publication: 2019 Mar 28 (Print Publication: 2019).
Publication Year :
2019

Abstract

Background: The minor allele ( C ) of the single-nucleotide polymorphism (SNP) rs11212617 , located near the ataxia telangiectasia mutated ( ATM ) gene, has been associated with an increased likelihood of treatment success with metformin in type 2 diabetes. We herein investigated whether the same SNP would predict clinical response to neoadjuvant metformin in women with early breast cancer (BC). Methods: DNA was collected from 79 patients included in the intention-to-treat population of the METTEN study, a phase 2 clinical trial of HER2-positive BC patients randomized to receive either metformin combined with anthracycline/taxane-based chemotherapy and trastuzumab or equivalent regimen without metformin, before surgery. SNP rs11212617 genotyping was assessed using allelic discrimination by quantitative polymerase chain reaction. Results: Logistic regression analyses revealed a significant relationship between the rs11212617 genotype and the ability of treatment arms to achieve a pathological complete response (pCR) in patients (odds ratio [OR] <subscript>genotype×arm</subscript> = 10.33, 95% confidence interval [CI]: 1.29-82.89, p = 0.028). In the metformin-containing arm, patients bearing the rs11212617 C allele had a significantly higher probability of pCR (OR <subscript> A / C,C / C </subscript> = 7.94, 95%CI: 1.60-39.42, p = 0.011). Conversely, no association was found between rs11212617 and clinical response in the reference arm (OR <subscript> A / C,C / C </subscript> = 0.77, 95%CI: 0.20-2.92, p = 0.700). After controlling for tumor size and hormone receptor status, the rs11212617 C allele remained a significant predictor of pCR solely in the metformin-containing arm. Conclusions: If reproducible, the rs11212617 C allele might warrant consideration as a predictive clinical biomarker to inform the personalized use of metformin in BC patients. Trial Registration: EU Clinical Trials Register, EudraCT number 2011-000490-30. Registered 28 February 2011, https://www.clinicaltrialsregister.eu/ctr-search/trial/2011-000490-30/ES.

Details

Language :
English
ISSN :
2234-943X
Volume :
9
Database :
MEDLINE
Journal :
Frontiers in oncology
Publication Type :
Academic Journal
Accession number :
30984619
Full Text :
https://doi.org/10.3389/fonc.2019.00193