Sustained effect of the aromatase inhibitors anastrozole and letrozole on endometrial thickness in patients with endometrial hyperplasia and endometrial carcinoma

ABSTRACT Objective: To investigate whether there may be a role for aromatase inhibitors (AIs) in the treatment of endometrial hyperplasia (EH) and endometrial adenocarcinoma (EA) in postmenopausal women, a retrospective study on the effect of aromatase inhibitors (anastrozole or letrozole) was conducted for 16 patients who were not amenable to surgical treatment. Main outcome measure: Resolution of endometrial thickening measured by transvaginal ultrasound at 3-month intervals; the response of metastases was assessed by standard oncological criteria. Results: In all, 16 patients were studied. The BMI of 13 of the 16 patients was known and ranged from 20.7 to 47.7 (mean 34.5) kg/m2 During treatment with AIs, mean endometrial thickness in the eight patients with EH decreased progressively by 81.7% from 14.7 mm at the start of treatment to 2.7 mm following 36 months of treatment. A greater original mean endometrial thickness of 17 mm was seen in the four patients with localised EA, this fell progressively by 67.1% to 5.6 mm following 36 months of treatment. No responses were seen in four patients with metastatic disease. Conclusion: Our results indicate that treatment of EH with anastrozole or letrozole can reduce endometrial thickness as seen ultrasonically, and that in some cases AI treatment can reduce endometrial thickness in patients with localised EA. We found no evidence to indicate that AI treatment prevents disease progression in patients with metastatic EA. Further investigations will be necessary to validate our findings from this small retrospective study and to compare AI inhibitor treatment with topical progestogen therapy.

[1]  A. Ørbo,et al.  Treatment results of endometrial hyperplasia after prospective D-score classification: a follow-up study comparing effect of LNG-IUD and oral progestins versus observation only. , 2008, Gynecologic oncology.

[2]  T. J. Clark,et al.  The effectiveness of a levonorgestrel-releasing intrauterine system (LNG-IUS) in the treatment of endometrial hyperplasia--a long-term follow-up study. , 2008, European journal of obstetrics, gynecology, and reproductive biology.

[3]  G. Garuti,et al.  Prospective endometrial assessment of breast cancer patients treated with third generation aromatase inhibitors. , 2006, Gynecologic oncology.

[4]  T. Agorastos,et al.  Aromatase inhibitor anastrozole for treating endometrial hyperplasia in obese postmenopausal women. , 2005, European journal of obstetrics, gynecology, and reproductive biology.

[5]  M. Dowsett,et al.  Double-blind, randomised, multicentre endocrine trial comparing two letrozole doses, in postmenopausal breast cancer patients. , 1999, European journal of cancer.

[6]  G. Grimbizis,et al.  Regression of endometrial hyperplasia after treatment with the gonadotrophin-releasing hormone analogue triptorelin: a prospective study. , 1999, Human reproduction.

[7]  P. Lønning,et al.  Influence of anastrozole (Arimidex), a selective, non-steroidal aromatase inhibitor, on in vivo aromatisation and plasma oestrogen levels in postmenopausal women with breast cancer. , 1996, British Journal of Cancer.

[8]  M. Blankenstein,et al.  A comparative study of risk factors for hyperplasia and cancer of the endometrium , 1996, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

[9]  T. Chard,et al.  The role of vaginal scan in measurement of endometrial thickness in postmenopausal women , 1991, British journal of obstetrics and gynaecology.