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Treatment of hormone positive uterine leiomyosarcoma with aromatase inhibitors

BACKGROUND: Aromatase inhibitors (AIs) have not been used consistently as part of the management of hormone receptor positive uterine leiomyosarcomas (ULMS). As a result, the published data regarding the efficacy of AIs in this subtype of ULMS are sparse. METHODS: We performed a retrospective electr...

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Autores principales: Thanopoulou, Eirini, Thway, Khin, Khabra, Komel, Judson, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094538/
https://www.ncbi.nlm.nih.gov/pubmed/25018868
http://dx.doi.org/10.1186/2045-3329-4-5
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author Thanopoulou, Eirini
Thway, Khin
Khabra, Komel
Judson, Ian
author_facet Thanopoulou, Eirini
Thway, Khin
Khabra, Komel
Judson, Ian
author_sort Thanopoulou, Eirini
collection PubMed
description BACKGROUND: Aromatase inhibitors (AIs) have not been used consistently as part of the management of hormone receptor positive uterine leiomyosarcomas (ULMS). As a result, the published data regarding the efficacy of AIs in this subtype of ULMS are sparse. METHODS: We performed a retrospective electronic medical record review of patients with ULMS treated with an AI, in the 1st or the 2nd line setting, at the Sarcoma Unit of the Royal Marsden Hospital between 2001 and 2012. We assessed progression-free survival (PFS), objective response and toxicities and explored the correlation of the intensity of the hormone receptor status, as well as of the grade with PFS. RESULTS: Sixteen patients with measurable advanced ULMS were treated with an AI in our unit. All of them were oestrogen receptor (ER) and progesterone receptor (PgR) positive. Letrozole was used in all patients as 1st line endocrine therapy, while exemestane was mainly prescribed as 2nd line (83%). Median PFS in 1st line was 14 months (95% CI: 0 – 30 months), and prolonged PFS was more likely to be observed in patients with low grade compared to high grade ULMS (20 months vs. 11 months), and in moderately/strongly ER positive compared to weakly ER positive ULMS (20 months vs. 12 months). Best response was partial response (PR) in 2/16 patients (12.5%) and clinical benefit (CB), defined as complete response (CR) + PR + stable disease ≥6 months, was observed in 10/16 patients (CB rate (CBR) 62.5%). Median duration of 2nd line was 3 months and median PFS was not reached. The 1-year progression-free rate for the 2nd line AI was 80%. Best response was PR in one patient and CBR was 50%. AIs were well tolerated in both lines of treatment. CONCLUSIONS: In this population of patients with hormone positive ULMS, AIs achieved a significant CBR (62.5%) in 1st line, which was retained in 2nd line (CBR: 50%). The relatively prolonged median PFS (14 months), along with the favourable toxicity profile could place AIs among the first choices of systemic treatment in hormone positive ULMS, preferably in strongly positive (>90%), and/ or low grade and low volume disease.
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spelling pubmed-40945382014-07-12 Treatment of hormone positive uterine leiomyosarcoma with aromatase inhibitors Thanopoulou, Eirini Thway, Khin Khabra, Komel Judson, Ian Clin Sarcoma Res Research BACKGROUND: Aromatase inhibitors (AIs) have not been used consistently as part of the management of hormone receptor positive uterine leiomyosarcomas (ULMS). As a result, the published data regarding the efficacy of AIs in this subtype of ULMS are sparse. METHODS: We performed a retrospective electronic medical record review of patients with ULMS treated with an AI, in the 1st or the 2nd line setting, at the Sarcoma Unit of the Royal Marsden Hospital between 2001 and 2012. We assessed progression-free survival (PFS), objective response and toxicities and explored the correlation of the intensity of the hormone receptor status, as well as of the grade with PFS. RESULTS: Sixteen patients with measurable advanced ULMS were treated with an AI in our unit. All of them were oestrogen receptor (ER) and progesterone receptor (PgR) positive. Letrozole was used in all patients as 1st line endocrine therapy, while exemestane was mainly prescribed as 2nd line (83%). Median PFS in 1st line was 14 months (95% CI: 0 – 30 months), and prolonged PFS was more likely to be observed in patients with low grade compared to high grade ULMS (20 months vs. 11 months), and in moderately/strongly ER positive compared to weakly ER positive ULMS (20 months vs. 12 months). Best response was partial response (PR) in 2/16 patients (12.5%) and clinical benefit (CB), defined as complete response (CR) + PR + stable disease ≥6 months, was observed in 10/16 patients (CB rate (CBR) 62.5%). Median duration of 2nd line was 3 months and median PFS was not reached. The 1-year progression-free rate for the 2nd line AI was 80%. Best response was PR in one patient and CBR was 50%. AIs were well tolerated in both lines of treatment. CONCLUSIONS: In this population of patients with hormone positive ULMS, AIs achieved a significant CBR (62.5%) in 1st line, which was retained in 2nd line (CBR: 50%). The relatively prolonged median PFS (14 months), along with the favourable toxicity profile could place AIs among the first choices of systemic treatment in hormone positive ULMS, preferably in strongly positive (>90%), and/ or low grade and low volume disease. BioMed Central 2014-06-26 /pmc/articles/PMC4094538/ /pubmed/25018868 http://dx.doi.org/10.1186/2045-3329-4-5 Text en Copyright © 2014 Thanopoulou et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Thanopoulou, Eirini
Thway, Khin
Khabra, Komel
Judson, Ian
Treatment of hormone positive uterine leiomyosarcoma with aromatase inhibitors
title Treatment of hormone positive uterine leiomyosarcoma with aromatase inhibitors
title_full Treatment of hormone positive uterine leiomyosarcoma with aromatase inhibitors
title_fullStr Treatment of hormone positive uterine leiomyosarcoma with aromatase inhibitors
title_full_unstemmed Treatment of hormone positive uterine leiomyosarcoma with aromatase inhibitors
title_short Treatment of hormone positive uterine leiomyosarcoma with aromatase inhibitors
title_sort treatment of hormone positive uterine leiomyosarcoma with aromatase inhibitors
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094538/
https://www.ncbi.nlm.nih.gov/pubmed/25018868
http://dx.doi.org/10.1186/2045-3329-4-5
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