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Aromatase inhibitor therapy for endometrial stromal sarcoma — two-centre experience
- Department of Oncology and Radiotherapy, Medical University of Gdansk, Poland
- Department of Gynecology, Oncology and Gynecologic Endocrinology, Medical University of Gdańsk, Poland
- Regional Center of Oncology COPERNICUS, Gdańsk, Poland
- Department of Pathology, Medical University of Gdańsk, Poland
open access
Abstract
Objectives: Endocrine therapy is the recommended systemic treatment for steroid receptor positive endometrial stromal
sarcoma (ESS). There is no current consensus on the optimal hormonal therapy for ESS. The literature offers several reports on advanced/recurrent/metastatic ESS patients treated with progestins, whereas data on the efficacy of aromatase inhibitors are scarce.
Material and methods: We retrospectively identified cases treated for ESS with aromatase inhibitors at our institutions. There were five patients with advanced or unresectable recurrent estrogen, progesterone and androgen receptor-positive ESS, treated with aromatase inhibitors: letrozole or anastrozole (at a daily dose of 2.5 mg and 1 mg, respectively), as first-line endocrine therapy in all but one case treated following progression with megestrol acetate.
Results: Disease stabilization was achieved in four cases (80%), including two with long-term progression-free survival
for up to 10 years attained under letrozole treatment, and one case after prior progestin treatment. During therapy, no
substantial toxicity was observed.
Conclusions: Aromatase inhibitors as first- or second-line endocrine treatment achieve disease control in most steroid
receptor positive ESS. Our series of cases is evidence of aromatase inhibitors efficacy as long-term endocrine treatment
option for ESS patients.
Abstract
Objectives: Endocrine therapy is the recommended systemic treatment for steroid receptor positive endometrial stromal
sarcoma (ESS). There is no current consensus on the optimal hormonal therapy for ESS. The literature offers several reports on advanced/recurrent/metastatic ESS patients treated with progestins, whereas data on the efficacy of aromatase inhibitors are scarce.
Material and methods: We retrospectively identified cases treated for ESS with aromatase inhibitors at our institutions. There were five patients with advanced or unresectable recurrent estrogen, progesterone and androgen receptor-positive ESS, treated with aromatase inhibitors: letrozole or anastrozole (at a daily dose of 2.5 mg and 1 mg, respectively), as first-line endocrine therapy in all but one case treated following progression with megestrol acetate.
Results: Disease stabilization was achieved in four cases (80%), including two with long-term progression-free survival
for up to 10 years attained under letrozole treatment, and one case after prior progestin treatment. During therapy, no
substantial toxicity was observed.
Conclusions: Aromatase inhibitors as first- or second-line endocrine treatment achieve disease control in most steroid
receptor positive ESS. Our series of cases is evidence of aromatase inhibitors efficacy as long-term endocrine treatment
option for ESS patients.
Keywords
endometrial stromal sarcoma; endocrine therapy; aromatase inhibitors
Title
Aromatase inhibitor therapy for endometrial stromal sarcoma — two-centre experience
Journal
Issue
Article type
Research paper
Pages
607-610
Published online
2018-11-30
Page views
1667
Article views/downloads
1594
DOI
Pubmed
Bibliographic record
Ginekol Pol 2018;89(11):607-610.
Keywords
endometrial stromal sarcoma
endocrine therapy
aromatase inhibitors
Authors
Krystyna Serkies
Anna Abacjew-Chmyłko
Magdalena Wieczorek-Rutkowska
Rafał Pęksa
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