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Aromatase inhibitor-induced modulation of breast density: clinical and genetic effects

BACKGROUND: Change in breast density may predict outcome of women receiving adjuvant hormone therapy for breast cancer. We performed a prospective clinical trial to evaluate the impact of inherited variants in genes involved in oestrogen metabolism and signalling on change in mammographic percent de...

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Autores principales: Henry, N L, Chan, H-P, Dantzer, J, Goswami, C P, Li, L, Skaar, T C, Rae, J M, Desta, Z, Khouri, N, Pinsky, R, Oesterreich, S, Zhou, C, Hadjiiski, L, Philips, S, Robarge, J, Nguyen, A T, Storniolo, A M, Flockhart, D A, Hayes, D F, Helvie, M A, Stearns, V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817329/
https://www.ncbi.nlm.nih.gov/pubmed/24084768
http://dx.doi.org/10.1038/bjc.2013.587
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author Henry, N L
Chan, H-P
Dantzer, J
Goswami, C P
Li, L
Skaar, T C
Rae, J M
Desta, Z
Khouri, N
Pinsky, R
Oesterreich, S
Zhou, C
Hadjiiski, L
Philips, S
Robarge, J
Nguyen, A T
Storniolo, A M
Flockhart, D A
Hayes, D F
Helvie, M A
Stearns, V
author_facet Henry, N L
Chan, H-P
Dantzer, J
Goswami, C P
Li, L
Skaar, T C
Rae, J M
Desta, Z
Khouri, N
Pinsky, R
Oesterreich, S
Zhou, C
Hadjiiski, L
Philips, S
Robarge, J
Nguyen, A T
Storniolo, A M
Flockhart, D A
Hayes, D F
Helvie, M A
Stearns, V
author_sort Henry, N L
collection PubMed
description BACKGROUND: Change in breast density may predict outcome of women receiving adjuvant hormone therapy for breast cancer. We performed a prospective clinical trial to evaluate the impact of inherited variants in genes involved in oestrogen metabolism and signalling on change in mammographic percent density (MPD) with aromatase inhibitor (AI) therapy. METHODS: Postmenopausal women with breast cancer who were initiating adjuvant AI therapy were enrolled onto a multicentre, randomised clinical trial of exemestane vs letrozole, designed to identify associations between AI-induced change in MPD and single-nucleotide polymorphisms in candidate genes. Subjects underwent unilateral craniocaudal mammography before and following 24 months of treatment. RESULTS: Of the 503 enrolled subjects, 259 had both paired mammograms at baseline and following 24 months of treatment and evaluable DNA. We observed a statistically significant decrease in mean MPD from 17.1 to 15.1% (P<0.001), more pronounced in women with baseline MPD ⩾20%. No AI-specific difference in change in MPD was identified. No significant associations between change in MPD and inherited genetic variants were observed. CONCLUSION: Subjects with higher baseline MPD had a greater average decrease in MPD with AI therapy. There does not appear to be a substantial effect of inherited variants in biologically selected candidate genes.
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spelling pubmed-38173292014-10-29 Aromatase inhibitor-induced modulation of breast density: clinical and genetic effects Henry, N L Chan, H-P Dantzer, J Goswami, C P Li, L Skaar, T C Rae, J M Desta, Z Khouri, N Pinsky, R Oesterreich, S Zhou, C Hadjiiski, L Philips, S Robarge, J Nguyen, A T Storniolo, A M Flockhart, D A Hayes, D F Helvie, M A Stearns, V Br J Cancer Clinical Study BACKGROUND: Change in breast density may predict outcome of women receiving adjuvant hormone therapy for breast cancer. We performed a prospective clinical trial to evaluate the impact of inherited variants in genes involved in oestrogen metabolism and signalling on change in mammographic percent density (MPD) with aromatase inhibitor (AI) therapy. METHODS: Postmenopausal women with breast cancer who were initiating adjuvant AI therapy were enrolled onto a multicentre, randomised clinical trial of exemestane vs letrozole, designed to identify associations between AI-induced change in MPD and single-nucleotide polymorphisms in candidate genes. Subjects underwent unilateral craniocaudal mammography before and following 24 months of treatment. RESULTS: Of the 503 enrolled subjects, 259 had both paired mammograms at baseline and following 24 months of treatment and evaluable DNA. We observed a statistically significant decrease in mean MPD from 17.1 to 15.1% (P<0.001), more pronounced in women with baseline MPD ⩾20%. No AI-specific difference in change in MPD was identified. No significant associations between change in MPD and inherited genetic variants were observed. CONCLUSION: Subjects with higher baseline MPD had a greater average decrease in MPD with AI therapy. There does not appear to be a substantial effect of inherited variants in biologically selected candidate genes. Nature Publishing Group 2013-10-29 2013-10-01 /pmc/articles/PMC3817329/ /pubmed/24084768 http://dx.doi.org/10.1038/bjc.2013.587 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Clinical Study
Henry, N L
Chan, H-P
Dantzer, J
Goswami, C P
Li, L
Skaar, T C
Rae, J M
Desta, Z
Khouri, N
Pinsky, R
Oesterreich, S
Zhou, C
Hadjiiski, L
Philips, S
Robarge, J
Nguyen, A T
Storniolo, A M
Flockhart, D A
Hayes, D F
Helvie, M A
Stearns, V
Aromatase inhibitor-induced modulation of breast density: clinical and genetic effects
title Aromatase inhibitor-induced modulation of breast density: clinical and genetic effects
title_full Aromatase inhibitor-induced modulation of breast density: clinical and genetic effects
title_fullStr Aromatase inhibitor-induced modulation of breast density: clinical and genetic effects
title_full_unstemmed Aromatase inhibitor-induced modulation of breast density: clinical and genetic effects
title_short Aromatase inhibitor-induced modulation of breast density: clinical and genetic effects
title_sort aromatase inhibitor-induced modulation of breast density: clinical and genetic effects
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817329/
https://www.ncbi.nlm.nih.gov/pubmed/24084768
http://dx.doi.org/10.1038/bjc.2013.587
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