PMID- 20832294 OWN - NLM STAT- MEDLINE DCOM- 20110328 LR - 20181201 IS - 1879-0852 (Electronic) IS - 0959-8049 (Linking) VI - 46 IP - 16 DP - 2010 Nov TI - Suppression of ovarian function in combination with an aromatase inhibitor as treatment for advanced breast cancer in pre-menopausal women. PG - 2936-42 LID - 10.1016/j.ejca.2010.08.005 [doi] AB - Trials have shown superiority of aromatase inhibitors (AIs) over tamoxifen for post-menopausal oestrogen receptor-positive advanced breast cancer (ER+ABC). We previously reported the use of goserelin plus anastrozole (G+A) as second-line endocrine therapy for pre-menopausal ER+ABC. We report clinical and endocrine data from G+A as first-line systemic therapy. Thirty-six patients (median age=44 years) with metastatic (N=28) and locally advanced disease were administered G+A for >/=6 months (unless progressed prior). Some (N=13) received further therapy with goserelin plus another AI (steroidal), exemestane (G+E). Serial serum hormone assays (oestradiol, dehydroepiandrosterone sulphate, testosterone, follicle stimulating hormone and luteinising hormone) were performed. Twenty-four patients (67%) derived clinical benefit (CB) (5% complete response, 31% partial response, 31% stable disease for >/=6 months) with median time to progression and duration of CB of 12 (2-47) and 24+(7-78+) months respectively. Ten patients were still receiving first-line G+A at analysis. Amongst 13 patients who went onto receive G+E, 38% achieved CB with a mean duration of 13+(7-32) months. Therapy was well tolerated with no withdrawals. The combination of G+A resulted in 98% reduction (from pre-treatment to 6-month) in median levels of oestradiol (from 574.5 pmol/L; inter-quartile range (IQR)=209-1426; (N=6) to 13.45 pmol/L; IOQ=5.5-31.5 (N=4) whilst the levels of other hormones had minimal fluctuations during therapy. The combinations of ovarian function suppression (using G) and AIs produce sustained CB and minimal side effects in pre-menopausal ER+ABC with significant reduction in oestradiol levels. Within the limitations of being a non-randomised study, they should be considered in appropriate patients with hormone-sensitive ABC. CI - Copyright (c) 2010 Elsevier Ltd. All rights reserved. FAU - Cheung, K L AU - Cheung KL AD - Division of Breast Surgery, University of Nottingham, UK. kl.cheung@nottingham.ac.uk FAU - Agrawal, A AU - Agrawal A FAU - Folkerd, E AU - Folkerd E FAU - Dowsett, M AU - Dowsett M FAU - Robertson, J F R AU - Robertson JF FAU - Winterbottom, L AU - Winterbottom L LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20100909 PL - England TA - Eur J Cancer JT - European journal of cancer (Oxford, England : 1990) JID - 9005373 RN - 0 (Androstadienes) RN - 0 (Aromatase Inhibitors) RN - 0 (Hormones) RN - 0 (Nitriles) RN - 0 (Triazoles) RN - 094ZI81Y45 (Tamoxifen) RN - 0F65R8P09N (Goserelin) RN - 2Z07MYW1AZ (Anastrozole) RN - 33515-09-2 (Gonadotropin-Releasing Hormone) RN - NY22HMQ4BX (exemestane) SB - IM CIN - Eur J Cancer. 2010 Nov;46(16):2867-9. PMID: 20880696 MH - Adult MH - Anastrozole MH - Androstadienes/administration & dosage MH - Antineoplastic Combined Chemotherapy Protocols/*therapeutic use MH - Aromatase Inhibitors/administration & dosage MH - Breast Neoplasms/*drug therapy MH - Female MH - Gonadotropin-Releasing Hormone MH - Goserelin/administration & dosage MH - Hormones/metabolism MH - Humans MH - Middle Aged MH - Nitriles/administration & dosage MH - Ovary/*drug effects MH - Premenopause MH - Tamoxifen/administration & dosage MH - Triazoles/administration & dosage EDAT- 2010/09/14 06:00 MHDA- 2011/03/29 06:00 CRDT- 2010/09/14 06:00 PHST- 2010/05/26 00:00 [received] PHST- 2010/07/28 00:00 [revised] PHST- 2010/08/09 00:00 [accepted] PHST- 2010/09/14 06:00 [entrez] PHST- 2010/09/14 06:00 [pubmed] PHST- 2011/03/29 06:00 [medline] AID - S0959-8049(10)00786-0 [pii] AID - 10.1016/j.ejca.2010.08.005 [doi] PST - ppublish SO - Eur J Cancer. 2010 Nov;46(16):2936-42. doi: 10.1016/j.ejca.2010.08.005. Epub 2010 Sep 9.