Cargando…

Quantitative Serial MRI of the Treated Fibroid Uterus

OBJECTIVE: There are no long-term medical treatments for uterine fibroids, and non-invasive biomarkers are needed to evaluate novel therapeutic interventions. The aim of this study was to determine whether serial dynamic contrast-enhanced MRI (DCE-MRI) and magnetization transfer MRI (MT-MRI) are abl...

Descripción completa

Detalles Bibliográficos
Autores principales: Munro, Kirsty I., Thrippleton, Michael J., Williams, Alistair R. W., McKillop, Graham, Walker, Jane, Horne, Andrew W., Newby, David E., Anderson, Richard A., Semple, Scott I., Marshall, Ian, Lewis, Steff C., Millar, Robert P., Bastin, Mark E., Critchley, Hilary O. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946427/
https://www.ncbi.nlm.nih.gov/pubmed/24608161
http://dx.doi.org/10.1371/journal.pone.0089809
_version_ 1782306647051337728
author Munro, Kirsty I.
Thrippleton, Michael J.
Williams, Alistair R. W.
McKillop, Graham
Walker, Jane
Horne, Andrew W.
Newby, David E.
Anderson, Richard A.
Semple, Scott I.
Marshall, Ian
Lewis, Steff C.
Millar, Robert P.
Bastin, Mark E.
Critchley, Hilary O. D.
author_facet Munro, Kirsty I.
Thrippleton, Michael J.
Williams, Alistair R. W.
McKillop, Graham
Walker, Jane
Horne, Andrew W.
Newby, David E.
Anderson, Richard A.
Semple, Scott I.
Marshall, Ian
Lewis, Steff C.
Millar, Robert P.
Bastin, Mark E.
Critchley, Hilary O. D.
author_sort Munro, Kirsty I.
collection PubMed
description OBJECTIVE: There are no long-term medical treatments for uterine fibroids, and non-invasive biomarkers are needed to evaluate novel therapeutic interventions. The aim of this study was to determine whether serial dynamic contrast-enhanced MRI (DCE-MRI) and magnetization transfer MRI (MT-MRI) are able to detect changes that accompany volume reduction in patients administered GnRH analogue drugs, a treatment which is known to reduce fibroid volume and perfusion. Our secondary aim was to determine whether rapid suppression of ovarian activity by combining GnRH agonist and antagonist therapies results in faster volume reduction. METHODS: Forty women were assessed for eligibility at gynaecology clinics in the region, of whom thirty premenopausal women scheduled for hysterectomy due to symptomatic fibroids were randomized to three groups, receiving (1) GnRH agonist (Goserelin), (2) GnRH agonist+GnRH antagonist (Goserelin and Cetrorelix) or (3) no treatment. Patients were monitored by serial structural, DCE-MRI and MT-MRI, as well as by ultrasound and serum oestradiol concentration measurements from enrolment to hysterectomy (approximately 3 months). RESULTS: A volumetric treatment effect assessed by structural MRI occurred by day 14 of treatment (9% median reduction versus 9% increase in untreated women; P = 0.022) and persisted throughout. Reduced fibroid perfusion and permeability assessed by DCE-MRI occurred later and was demonstrable by 2–3 months (43% median reduction versus 20% increase respectively; P = 0.0093). There was no apparent treatment effect by MT-MRI. Effective suppression of oestradiol was associated with early volume reduction at days 14 (P = 0.041) and 28 (P = 0.0061). CONCLUSION: DCE-MRI is sensitive to the vascular changes thought to accompany successful GnRH analogue treatment of uterine fibroids and should be considered for use in future mechanism/efficacy studies of proposed fibroid drug therapies. GnRH antagonist administration does not appear to accelerate volume reduction, though our data do support the role of oestradiol suppression in GnRH analogue treatment of fibroids. TRIAL REGISTRATION: ClinicalTrials.gov NCT00746031
format Online
Article
Text
id pubmed-3946427
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-39464272014-03-10 Quantitative Serial MRI of the Treated Fibroid Uterus Munro, Kirsty I. Thrippleton, Michael J. Williams, Alistair R. W. McKillop, Graham Walker, Jane Horne, Andrew W. Newby, David E. Anderson, Richard A. Semple, Scott I. Marshall, Ian Lewis, Steff C. Millar, Robert P. Bastin, Mark E. Critchley, Hilary O. D. PLoS One Research Article OBJECTIVE: There are no long-term medical treatments for uterine fibroids, and non-invasive biomarkers are needed to evaluate novel therapeutic interventions. The aim of this study was to determine whether serial dynamic contrast-enhanced MRI (DCE-MRI) and magnetization transfer MRI (MT-MRI) are able to detect changes that accompany volume reduction in patients administered GnRH analogue drugs, a treatment which is known to reduce fibroid volume and perfusion. Our secondary aim was to determine whether rapid suppression of ovarian activity by combining GnRH agonist and antagonist therapies results in faster volume reduction. METHODS: Forty women were assessed for eligibility at gynaecology clinics in the region, of whom thirty premenopausal women scheduled for hysterectomy due to symptomatic fibroids were randomized to three groups, receiving (1) GnRH agonist (Goserelin), (2) GnRH agonist+GnRH antagonist (Goserelin and Cetrorelix) or (3) no treatment. Patients were monitored by serial structural, DCE-MRI and MT-MRI, as well as by ultrasound and serum oestradiol concentration measurements from enrolment to hysterectomy (approximately 3 months). RESULTS: A volumetric treatment effect assessed by structural MRI occurred by day 14 of treatment (9% median reduction versus 9% increase in untreated women; P = 0.022) and persisted throughout. Reduced fibroid perfusion and permeability assessed by DCE-MRI occurred later and was demonstrable by 2–3 months (43% median reduction versus 20% increase respectively; P = 0.0093). There was no apparent treatment effect by MT-MRI. Effective suppression of oestradiol was associated with early volume reduction at days 14 (P = 0.041) and 28 (P = 0.0061). CONCLUSION: DCE-MRI is sensitive to the vascular changes thought to accompany successful GnRH analogue treatment of uterine fibroids and should be considered for use in future mechanism/efficacy studies of proposed fibroid drug therapies. GnRH antagonist administration does not appear to accelerate volume reduction, though our data do support the role of oestradiol suppression in GnRH analogue treatment of fibroids. TRIAL REGISTRATION: ClinicalTrials.gov NCT00746031 Public Library of Science 2014-03-07 /pmc/articles/PMC3946427/ /pubmed/24608161 http://dx.doi.org/10.1371/journal.pone.0089809 Text en © 2014 Munro et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Munro, Kirsty I.
Thrippleton, Michael J.
Williams, Alistair R. W.
McKillop, Graham
Walker, Jane
Horne, Andrew W.
Newby, David E.
Anderson, Richard A.
Semple, Scott I.
Marshall, Ian
Lewis, Steff C.
Millar, Robert P.
Bastin, Mark E.
Critchley, Hilary O. D.
Quantitative Serial MRI of the Treated Fibroid Uterus
title Quantitative Serial MRI of the Treated Fibroid Uterus
title_full Quantitative Serial MRI of the Treated Fibroid Uterus
title_fullStr Quantitative Serial MRI of the Treated Fibroid Uterus
title_full_unstemmed Quantitative Serial MRI of the Treated Fibroid Uterus
title_short Quantitative Serial MRI of the Treated Fibroid Uterus
title_sort quantitative serial mri of the treated fibroid uterus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946427/
https://www.ncbi.nlm.nih.gov/pubmed/24608161
http://dx.doi.org/10.1371/journal.pone.0089809
work_keys_str_mv AT munrokirstyi quantitativeserialmriofthetreatedfibroiduterus
AT thrippletonmichaelj quantitativeserialmriofthetreatedfibroiduterus
AT williamsalistairrw quantitativeserialmriofthetreatedfibroiduterus
AT mckillopgraham quantitativeserialmriofthetreatedfibroiduterus
AT walkerjane quantitativeserialmriofthetreatedfibroiduterus
AT horneandreww quantitativeserialmriofthetreatedfibroiduterus
AT newbydavide quantitativeserialmriofthetreatedfibroiduterus
AT andersonricharda quantitativeserialmriofthetreatedfibroiduterus
AT semplescotti quantitativeserialmriofthetreatedfibroiduterus
AT marshallian quantitativeserialmriofthetreatedfibroiduterus
AT lewissteffc quantitativeserialmriofthetreatedfibroiduterus
AT millarrobertp quantitativeserialmriofthetreatedfibroiduterus
AT bastinmarke quantitativeserialmriofthetreatedfibroiduterus
AT critchleyhilaryod quantitativeserialmriofthetreatedfibroiduterus