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AI-related BMD variation in actual practice conditions: A prospective cohort study.

Authors :
Rodríguez-Sanz M
Prieto-Alhambra D
Servitja S
Garcia-Giralt N
Garrigos L
Rodriguez-Morera J
Albanell J
Martínez-García M
González I
Diez-Perez A
Tusquets I
Nogués X
Source :
Endocrine-related cancer [Endocr Relat Cancer] 2016 Apr; Vol. 23 (4), pp. 303-12. Date of Electronic Publication: 2016 Feb 24.
Publication Year :
2016

Abstract

The aim of the study was to evaluate the progression of bone mineral density (BMD) during 3 years of aromatase inhibitors (AI) therapy in actual practice conditions. This prospective, clinical cohort study of Barcelona-Aromatase induced Bone Loss in Early breast cancer (B-ABLE) assessed BMD changes during 3 years of AI treatment in women with breast cancer. Patients with osteoporosis (T score < -2.5 or T score ≤ -2.0) and a major risk factor and/or prevalent fragility fractures were treated with oral bisphosphonates (BPs). Of 685 women recruited, 179 (26.1%) received BP treatment. By the third year of AI therapy, this group exhibited increased BMD in the lumbar spine (LS; 2.59%) and femoral neck (FN; 2.50%), although the increase was significant only within the first year (LS: 1.99% and FN: 2.04%). Despite BP therapy, however, approximately 15% of these patients lost more than 3% of their baseline bone mass. At 3 years, patients without BP experienced BMD decreases in the LS (-3.10%) and FN (-2.79%). In this group, BMD changes occurred during the first (LS: -1.33% and FN: -1.25%), second (LS: -1.19% and FN: -0.82%), and third (LS: -0.57% and FN: -0.65%) years of AI treatment. Increased BMD (>3%) was observed in just 7.6% and 10.8% of these patients at the LS and FN, respectively. Our data confirm a clinically relevant bone loss associated with AI therapy amongst nonusers of preventative BPs. We further report on the importance of BMD monitoring as well as calcium and 25-hydroxy vitamin D supplementation in these patients.<br /> (© 2016 Society for Endocrinology.)

Details

Language :
English
ISSN :
1479-6821
Volume :
23
Issue :
4
Database :
MEDLINE
Journal :
Endocrine-related cancer
Publication Type :
Academic Journal
Accession number :
26911377
Full Text :
https://doi.org/10.1530/ERC-16-0025