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Diagnosis and Treatment of Patients with Primary and Metastatic Breast Cancer © AGO e. V. in der DGGG e.V. sowie in der DKG e.V. Guidelines Breast Version 2016.1 Endocrine and “Targeted” Therapy in Metastatic Breast Cancer Endocrine Therapy of Metastatic Breast Cancer © AGO e. V. in der DGGG e.V. sowie in der DKG e.V. Version 2002: Gerber / Friedrichs Versions 2003–2015: Albert / Bischoff / Dall / Fersis / Friedrich / Gerber / Huober / Janni / Jonat / Kaufmann / Liedtke / Loibl / Lück / von Minckwitz / Möbus / Müller / Mundhenke / Nitz / Schneeweiß / Schütz / Stickeler Version 2016: Hanf / Mundhenke Guidelines Breast Version 2016.1 www.ago-online.de Endocrine Therapy in Metastatic Breast Cancer © AGO Indication e. V. in der DGGG e.V. sowie in der DKG e.V. Oxford LoE: 1a Guidelines Breast Version 2016.1 GR: A AGO: ++ Endocrine therapy represents the first choice for metastatic breast cancer with positive (or unknown) hormone receptor (HR) status. www.ago-online.de Exception: acute life-threatening disease Caveat: HR might change during the course of disease. Histology of recurrent site should be obtained whenever possible Comparison ER/PR and HER2 Metastasis vs. Primary Tumor © AGO e. V. in der DGGG e.V. sowie in der DKG e.V. Guidelines Breast Version 2016.1 Meta-analysis based on 48 (mostly retrospective) analyses: Pooled discordance proportions were 20% (95%CI 16-35%) for ER 33% (95%CI 29-38%) for PR 8% (95% CI 6-10%) for HER2 www.ago-online.de Pooled proportions of tumors shifting from positive to negative and negative to positive were 4% and 14% for ER 46% and 15% for PR 13% and 5% for HER2 Endocrine Therapy General considerations © AGO e. V. in der DGGG e.V. sowie in der DKG e.V. Guidelines Breast Version 2016.1 Within all lines of treatment, treatment options should take previous endocrine therapies, age and comorbidities into consideration as well as respective approval status www.ago-online.de Endocrine Therapy in Premenopausal Patients with HER2-Negative Metastatic Breast Cancer © AGO e. V. in der DGGG e.V. sowie in der DKG e.V. Oxford / AGO LoE / GR Guidelines Breast Version 2016.1 www.ago-online.de GnRHa + tamoxifen (vs. OFS or Tam) 1a A ++ Ovarian function suppression (OFS) 2b B + Tamoxifen 2b B + GnRHa + AI (first or second line) 2b B + GnRHa + Fulvestrant 1b B + GnRHa + Fulvestrant +Palbociclib 1b B + Aromatase inhibitors without OFS 3 -- D Endocrine Therapy in Postmenopausal Patients with HER2-Negative Metastatic Breast Cancer © AGO e. V. in der DGGG e.V. sowie in der DKG e.V. Guidelines Breast Version 2016.1 *There is no evidence for superiority of a single aromatase inhibitor. As everolimus plus exemestane is indicated after AI treatment, a non-steroidal AI should be preferred in first line. MA§: Megestroleacetate, ** steroidal or non-steroidal resp. depending on previous AI Oxford / AGO LoE / GR 1b B ++ 1a A ++ 1a A ++ 1b B + Fulvestrant 500 mg Aromatase inhibitors (3rd gen) ** Tamoxifen Letrozole + Palbociclib Fulvestrant 500 mg plus Palbociclib 1b B + Exemestane + Everolimus 1b A + Tamoxifen + Everolimus MPA/MA§ Fulvestrant 250 mg + Anastrozol Estradiol valerate 2-6 mg daily 2b 1a 1b 2b B A B C + +/+/+/- Repeat prior treatments 5 D +/- www.ago-online.de Therapy Algorithm After Adjuvant Tamoxifen © AGO e. V. in der DGGG e.V. sowie in der DKG e.V. Guidelines Breast Version 2016.1 Fulvestrant 500 mg or Non-steroidal AI 3rd generation or Tamoxifen* Exemestane + everolimus www.ago-online.de Fulvestrant 500 mg +/Palbociclib Fulvestrant 500 mg +/- Palbociclib Exemestane + everolimus Tamoxifen Tamoxifen *(after long recurrence-free intervall) Therapy Algorithm After Adjuvant AI © AGO e. V. in der DGGG e.V. sowie in der DKG e.V. Short treatment free interval ≤12 months Long treatment free interval >12 months Guidelines Breast Version 2016.1 Exemestane + everolimus Fulvestrant 500 mg +/Palbociclib Fulvestrant 500 mg Exemestane + everolimus Tamoxifen www.ago-online.de Tamoxifen Tamoxifen Fulvestrant 500 mg + Palbociclib Endocrine Therapy in Postmenopausal HER2-Negative Metastatic Breast Cancer Patients in Combination with Bevacizumab © AGO e. V. Oxford / AGO LoE / GR in der DGGG e.V. sowie in der DKG e.V. Guidelines Breast Version 2016.1 www.ago-online.de Maintenance bevacizumab plus endocrine therapy after remission with chemotherapy and bevacizumab Bevacizumab plus endocrine treatment as first line therapy for advanced disease 2b B + 1b B - Diagnosis and Treatment of Patients with Primary and Metastatic Breast Cancer © AGO e. V. in der DGGG e.V. sowie in der DKG e.V. Guidelines Breast Version 2016.1 HER2 Positive and HR-Positive Metastatic Breast Cancer Endocrine Therapy in Postmenopausal HER2Positive Metastatic Breast Cancer Patients © AGO e. V. in der DGGG e.V. sowie in der DKG e.V. Oxford / AGO LoE / GR Guidelines Breast Version 2016.1 www.ago-online.de Anastrozole plus trastuzumab 1b Letrozole plus trastuzumab 2b Letrozole plus lapatinib 1b Fulvestrant plus lapatinib 1b Poor efficacy of endocrine therapy alone. B B B B Consider induction chemotherapy + anti-HER2-therapy! +/+/+/+/- Combination of Endocrine Treatment with Anti-HER2-Treatment © AGO e. V. in der DGGG e.V. sowie in der DKG e.V. Treatment (no. of pats) PFS (months) Response rate OS (months) (CBR) Trastuzumab + anastrozole vs. anastrozole (n=207) 4.8 vs. 2.4 (5.6 vs. 3.8 with centrally confirmed receptor status) 42.7% vs. 27.9% 28.5 vs. 23.9 mo; n.s. Trastuzumab + letrozole vs. letrozole (n=57) 14,1 vs. 3.3 27% vs. 13% not reported Lapatinib + letrozole vs. letrozole (n=219/1286) 8.2 vs. 3.0 48% v 29% 33.3 vs. 32.3 mo Lapatinib + fulvestrant vs. fulvestrant (n=146/145) 4.1 vs. 3.8 (HER2-) p: 0,25 5.9 vs. 3.3 (HER2+) p: 0,53 (CR +PR) 20 vs. 9% p: 0,048 30 vs. 26.4 mo (all), n.s. Guidelines Breast Version 2016.1 www.ago-online.de Concomitant or Sequential Endocrine-Cytostatic Treatment © AGO e. V. in der DGGG e.V. sowie in der DKG e.V. Oxford / AGO LoE / GR Guidelines Breast Version 2016.1 Concomitant endocrine-cytotoxic treatment - 2b B ++ May increase response rate and progression free interval but not overall survival www.ago-online.de 1b A May increase toxicity Maintenance endocrine therapy after chemotherapy induced response Increases progression free interval Endocrine and “Targeted” Therapy in Metastatic Breast Cancer (2/14) No further information No references Endocrine and “Targeted” Therapy in Metastatic Breast Cancer (3/14) No further information References: 1. 2. 3. 4. 5. 6. 7. Wilcken N, Hornbuckle J, Ghersi D Chemotherapy alone versus endocrine therapy alone for metastatic breast cancer. Cochrane Database Syst Rev. 2003;(2):CD002747. De Laurentiis M, et al.: A meta-analysis on the interaction between HER-2 expression and response to endocrine treatment in advanced breast cancer. Clin Cancer Res. 2005 Jul 1;11(13):4741-8 Thompson AM For the Breast Recurrence In Tissues Study (BRITS) A Prospective Comparison of Switches in Biomarker Status between Primary and Recurrent Breast Cancer: The Breast Recurrence in Tissues Study (BRITS). Cancer Res. Vol 69, No. 3 (suppl. 2), abstract 4053, http://www.abstracts2view.com/sabcs09/view.php?nu=SABCS09L_1530 Tomasevic ZI, Nikolic SS, Jevric M, Pupic G, Milovanovic Z, Skender M, Inic M, Tomasevic ZM, Djodic R, Zegarac M, Vasovic S, Jelic S Comparison between Steroid Receptors and Her2 Status in Primary Breast Carcinoma and Completely Resected Breast Carcinoma Metastases from Different Visceral Organ Sites. Cancer Res. Vol 69, No. 3 (suppl. 2), abstract 4048, http://www.abstracts2view.com/sabcs09/view.php?nu=SABCS09L_780 Broom RJ, Tang PA, Simmons C, Bordeleau L, Mulligan AM, O'Malley FP, Miller N, Andrulis IL, Brenner DM, Clemons MJ Changes in estrogen receptor, progesterone receptor and Her-2/neu status with time: discordance rates between primary and metastatic breast cancer. Anticancer Res. 2009 May;29(5):1557-62 Lower EE , Glass EL, Bradley DA, Blau R, Heffelfinger S Impact of metastatic estrogen receptor and progesterone receptor status on survival. Breast Cancer Res Treat. 2005 Mar;90(1):65-70. Li BD, Byskosh A, Molteni A, Duda RB Estrogen and progesterone receptor concordance between primary and recurrent breast cancer. J Surg Oncol. 1994 Oct;57(2):71-7. Comparison ER/PR and HER2 Metastasis vs. Primary Tumor (4/14) No further information References: 1. 2. 3. 4. 5. 6. 7. 8. Amir E, Miller N, et al. Prospective study evaluating the impact of tissue confirmation of metastatic disease in patients with breast cancer. J Clin Oncol. 2012; 30(6):587-92. Broom RJ, Tang PA, Simmons C, Bordeleau L, Mulligan AM, O'Malley FP, Miller N, Andrulis IL, Brenner DM, Clemons MJ Changes in estrogen receptor, progesterone receptor and Her-2/neu status with time: discordance rates between primary and metastatic breast cancer. Anticancer Res. 2009 May;29(5):1557-62 Chan A, Morey A, Brown B, Hastrich D, Willsher P, Ingram D. A retrospective study investigating the rate of HER2 discordance between primary breast carcinoma and locoregional or metastatic disease. BMC Cancer. 2012 Nov 24;12:555. Edgerton SM, Moore D 2nd, Merkel D, Thor AD. erbB-2 (HER-2) and breast cancer progression. Appl Immunohistochem Mol Morphol. 2003 Sep;11(3):214-21. Gancberg D1, Di Leo A, Cardoso F, Rouas G, Pedrocchi M, Paesmans M, Verhest A, Bernard-Marty C, Piccart MJ, Larsimont D. Comparison of HER-2 status between primary breast cancer and corresponding distant metastatic sites. Ann Oncol. 2002 Jul;13(7):1036-43. Liedtke C, Broglio K, Moulder S, Hsu L, Kau SW, Symmans WF, Albarracin C, Meric-Bernstam F, Woodward W, Theriault RL, Kiesel L, Hortobagyi GN, Pusztai L, Gonzalez-Angulo AM. Prognostic impact of discordance between triple-receptor measurements in primary and recurrent breast cancer. Ann Oncol. 2009 Dec;20(12):1953-8 Li BD, Byskosh A, Molteni A, Duda RB Estrogen and progesterone receptor concordance between primary and recurrent breast cancer. J Surg Oncol. 1994 Oct;57(2):71-7. Lindström LS, Karlsson E et al. Clinically used breast cancer markers such as estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 are unstable throughout tumor progression. J Clin Oncol. Jul 20;30(21):2601-8, 2012. 9. 10. 11. 12. 13. 14. 15. 16. Lower EE, Glass EL, Bradley DA, Blau R, Heffelfinger S. Impact of metastatic estrogen receptor and progesterone receptor status on survival. Breast Cancer Res Treat. 2005 Mar;90(1):65-70. Macfarlane R1, Seal M, Speers C, Woods R, Masoudi H, Aparicio S, Chia SK. Molecular alterations between the primary breast cancer and the subsequent locoregional/metastatic tumor. Oncologist. 2012;17(2):172-8. doi: 10.1634/theoncologist.2011-0127. Epub 2012 Jan 20. Nedergaard L1, Haerslev T, Jacobsen GK. Immunohistochemical study of estrogen receptors in primary breast carcinomas and their lymph node metastases including comparison of two monoclonal antibodies. APMIS. 1995 Jan;103(1):20-4. Niikura N, Liu J, et al. Loss of human epidermal growth factor receptor 2 (HER2) expression in metastatic sites of HER2-overexpressing primary breast tumors. J Clin OncolFeb 20;30(6):593-9, 2012. Tapia C, Savic S, Wagner U, Schönegg R, Novotny H, Grilli B, Herzog M, Barascud AD, Zlobec I, Cathomas G, Terracciano L, Feichter G, Bubendorf L. HER2 gene status in primary breast cancers and matched distant metastases. Breast Cancer Res. 2007;9(3):R31. Wilking U, Karlsson E, Skoog L, Hatschek T, Lidbrink E, Elmberger G, Johansson H, Lindström L, Bergh J. HER2 status in a population-derived breast cancer cohort: discordances during tumor progression. Breast Cancer Res Treat. 2011 Jan;125(2):553-61. Thompson AM, Jordan LB, Quinlan P, Anderson E, Skene A, Dewar JA, Purdie CA; Breast Recurrence in Tissues Study Group.Prospective comparison of switches in biomarker status between primary and recurrent breast cancer: the Breast Recurrence In Tissues Study (BRITS). Breast Cancer Res. 2010;12(6):R92 Tomasevic ZI, Nikolic SS, Jevric M, Pupic G, Milovanovic Z, Skender M, Inic M, Tomasevic ZM, Djodic R, Zegarac M, Vasovic S, Jelic S Comparison between Steroid Receptors and Her2 Status in Primary Breast Carcinoma and Completely Resected Breast Carcinoma Metastases from Different Visceral Organ Sites. Cancer Res. Vol 69, No. 3 (suppl. 2), abstract 4048, http://www.abstracts2view.com/sabcs09/view.php?nu=SABCS09L_780 Endocrine Therapy General Considerations (5/14) No further information References: „Aromatase inhibitors (3rd gen) (> non-AI*)“ 1. 2. 3. 4. 5. 6. Gibson L, Lawrence D, Dawson C, Bliss J. Aromatase inhibitors for treatment of advanced breast cancer in postmenopausal women. Cochrane Database Syst Rev. 2009 Oct 7;(4):CD003370. Ferretti G, Bria E, Giannarelli D, Felici A, Papaldo P, Fabi A, Di Cosimo S, Ruggeri EM, Milella M, Ciccarese M, Cecere FL, Gelibter A, Nuzzo C, Cognetti F, Terzoli E, Carlini P. Second- and third-generation aromatase inhibitors as first-line endocrine therapy in postmenopausal metastatic breast cancer patients: a pooled analysis of the randomised trials. Br J Cancer. 2006 Jun 19;94(12):1789-96 Nabholtz, JM, Buzdar, A, Pollak, M, Harwin, W, Burton, G, Mangalik, A, Anastrozole is superior to tamoxifen as firstline therapy for advanced breast cancer in postmenopausal women: results of a North American multicenter randomized trial. Journal of Clinical Oncology 2000 18 Thuerlimann, B, Robertson, JFR, Nabholtz, JM, Buzdar, A, Bonneterre, J, Efficacy of tamoxifen following anastrozole ('Arimidex') compared with anastrozole following tamoxifen as first-line treatment for advanced breast cancer in postmenopausal women European Journal of Cancer 2003 39 Bonneterre, J, Buzdar, A, Nabholtz, JA, Robertson, JFR, Thuerlimann, B, von Euler, M, Anastrozole is superior to tamoxifen as first-line therapy in hormone receptor positive advanced breast carcinoma Cancer 2001 92 Buzdar, A, Douma, J, Davidson, N, Elledge, R, Morgan, M, Smith, R, Phase III, multicenter, double-blind, randomized study of letrozole, an aromatase inhibitor, for advanced breast cancer versus megestrol acetate Journal of Clinical Oncology 2001 19 7. 8. 9. 10. Mourisden, H, Gershanovich, M, Sun, Y, Perez-Carrion, R, Boni, C, Monnier, A, Phase III study of letrozole versus tamoxifen as first-line therapy of advanced breast cancer in postmenopausal women: analysis of survival and update of efficacy from the International Letrozole Breast Cancer Group Journal of Clinical Oncology 2003 Kaufmann, M, Bajetta, E, Dirix, LY, Fein, LE, Jones, SE, Cervek, J, Exemestane improves survival compared with megestrol acetate in postmenopausal patients with advanced breast cancer who have failed on tamoxifen: results of a double-blind randomised phase III trial European Journal of Cancer 2000 36 Paridaens, R, Dirix, L, Lohrisch, C, Beex, L, Nooji, M, Cameron, D, Mature results of a randomized phase II multicenter study of exemextane versus tamoxifen as first-line hormone therapy for postmenopausal women with metastatic breast cancer Annals of Oncology 2003 14 Mauri, D, Pavlidis, N, Polyzos, NP, Ioannidis, JP, Survival with aromatase inhibitors and inactivators versus standard hormonal therapy in advanced breast cancer: meta-analysis Journal of the National Cancer Institute 2006 98 Fulvestran 250 mg (=AI) 1. 2. 3. 4. 5. Howell, A, Robertson, JFR, Quaresma Albano, J, Ascgermannova, A, Mauriac, L, Kleeberg, UR, Fulvestrant, formerly ICI 182, 780, is as effective as anastrozole in postmenopausal women with advanced breast cancer progressing after prior endocrine treatment Journal of Clinical Oncology 2002 20 Mauriac, L, Pippen, JE, Quaresma Albano, J, Gertler, SZ, Osborne, CK, Fulvestrant (Faslodex) versus anastrozole for the second-line treatment of advanced breast cancer in subgroups of postmenopausal women with visceral and nonvisceral metasteses: combined results from two multicentre trials European Journal of Cancer 2003 39 Osborne, CK, Pippen, J, Jones, SE, Parker, LM, Ellis, M, Come, S, Double-blind, randomized trial comparing the efficacy and tolerability of the fulvestrant versus anastrozole in postmenopausal women with advanced breast cancer progressing on prior endocrine therapy: results of a North American Trial Journal of Clinical Oncology 2002 20 Perey L, Paridaens R, Hawle H, Zaman K, Nolé F, Wildiers H, Fiche M, Dietrich D, Clément P, Köberle D, Goldhirsch A, Thürlimann B. Clinical benefit of fulvestrant in postmenopausal women with advanced breast cancer and primary or acquired resistance to aromatase inhibitors: final results of phase II Swiss Group for Clinical Cancer Research Trial (SAKK 21/00). Ann Oncol. 2007 Jan;18(1):64-9. Epub 2006 Oct 9. Chia S, Gradishar W, Mauriac L, Bines J, Amant F, Federico M, Fein L, Romieu G, Buzdar A, Robertson JF, Brufsky A, Possinger K, Rennie P, Sapunar F, Lowe E, Piccart M. Double-blind, randomized placebo controlled trial of 6. 7. 8. fulvestrant compared with exemestane after prior nonsteroidal aromatase inhibitor therapy in postmenopausal women with hormone receptor-positive, advanced breast cancer: results from EFECT. J Clin Oncol. 2008 Apr 1;26(10):166470. Mauriac L, Romieu G, Bines J. Activity of fulvestrant versus exemestane in advanced breast cancer patients with or without visceral metastases: data from the EFECT trial.Breast Cancer Res Treat. 2009 Sep;117(1):69-75. Bergh J, Jönsson PE, Lidbrink E, Trudeau M, Eiermann W, Brattström D, Lindemann J, Wiklund F, Henriksson R. First Results from FACT – An Open-Label, Randomized Phase III Study Investigating Loading Dose of Fulvestrant Combined with Anastrozole Versus Anastrozole at First Relapse in Hormone Receptor Positive Breast Cancer. Cancer Res. Vol 69, No. 3 (suppl. 2), abstract 23 Xu B, Jiang Z, Shao Z, Wang J, Feng J, Song S, Chen Z, Gu K, Yu S, Zhang Y, Wang C, Zhang F, Yang J. Fulvestrant 250 mg versus anastrozole for Chinese patients with advanced breast cancer: results of a multicentre, double-blind, randomised phase III trial. Cancer Chemother Pharmacol. 2011 Jan;67(1):223-30. Fulvestrant 500 mg 1. 2. 3. DiLeo A, Jerusalem G et al. Results of the CONFIRM Phase III Trial Comparing Fulvestrant 250 mg With Fulvestrant 500 mg in Postmenopausal Women With Estrogen Receptor–Positive Advanced Breast Cancer. JCO 28: 4594-4600, 2010 Di Leo A, Jerusalem G, Petruzelka L et al: Final overall survival: Fulvestrant 500 mg vs 250 mg in the randomized CONFIRM Trial. J Natl Cancer Inst.106:1-7(2014) Robertson JFR, Llombart-Cussac A, Feltl D et al: Fulvestrant 500 mg versus anastrozole as first-line treatment for advanced breast cancer: overall survival from the phase II ‚first‘ study. San Antonio Breast cancer Symposium S6-04 (2014) MPA/MA inferior to AI) 1. Budzar, A, Jonat, W, Howell, A, Jones, SE, Blomqvist, C, Vogel, CL, Anastrozole, a potent and selective aromatase inhibitor, versus megestrol acetate in postmenopausal women with advanced breast cancer: results of overview analysis of two phase III trials Journal of Clinical Oncology 1996 14 2. 3. 4. 5. 6. 7. Buzdar, AU, Jonat, W, Howell, A, Jones, SE, Blomqvist, CP, Vogel, CL, Anastrozole versus megestrol acetate in the treatment of postmenopausal women with advanced breast carcinoma Cancer 1998 83 Jonat, W, Howell, A, Blomqvist, C, Eiermann, W, Winblad, G, Tyrrell, C, A randomized trial comparing two doses of the new selective aromatase inhibitor anastrozole (Arimidex) with megestrol acetate in postmenopausal women with advanced breast cancer European Journal of Cancer 1996 32A Buzdar, A, Douma, J, Davidson, N, Elledge, R, Morgan, M, Smith, R, Phase III, multicenter, double-blind, randomized study of letrozole, an aromatase inhibitor, for advanced breast cancer versus megestrol acetate Journal of Clinical Oncology 2001 19 Goss, PE, Winer, EP, Tannock, IF, Schwarz, LH, Randomized phase III trial comparing the new potent and selective third generation aromatase inhibitor vorozole with megestrol acetate in postmenopausal advanced breast cancer patients Journal of Clinical Oncology 1999 17 Kaufmann, M, Bajetta, E, Dirix, LY, Fein, LE, Jones, SE, Cervek, J, Exemestane improves survival compared with megestrol acetate in postmenopausal patients with advanced breast cancer who have failed on tamoxifen: results of a double-blind randomised phase III trial European Journal of Cancer 2000 36 Kaufmann, M, Bajetta, E, Dirix, LY, Fein, LE, Jones, SE, Zilembo, N, Exemestane is superior to megestrol acetate after tamoxifen failure in postmenopausal women with advanced breast cancer: results of a phase III randomised doubleblind trial Journal of Clinical Oncology 2000 18 Comparison of different AI 1. 2. Rose C., Vtoraya O., Pluzanska A., Davidson N., Gershanovich M., Thomas R., Johnson S., Caicedo J.J., Gervasio H., Manikhas G., Ben Ayed F., Burdette-Radoux S., Chaudri-Ross H.A., Lang R.: An open randomised trial of second-line endocrine therapy in advanced breast cancer. comparison of the aromatase inhibitors letrozole and anastrozole. Eur J Cancer, Vol. 39: 2318-27, 2003. Tobias, JS, Howell, A, An open randomised trial of second-line endocrine therapy in advanced breast cancer: comparison of the aromatase inhibitors letrozole and anastrozole European Journal of Cancer (letter as comment to Ref 1) 2004 40 3. 4. Tominaga, T, Adachi, I, Sasaki, Y, Tabei, T, Ikeda, T, Takatsuka, Y, Double-blind randomised trial comparing the nonsteroidal aromatase inhibitors letrozole and fadrozole in postmenopausal women with advanced breast cancer Annals of Oncology 2003 14 Campos SM, Guastalla JP, Subar M, Abreu P, Winer EP, Cameron DA. A comparative study of exemestane versus anastrozole in patients with postmenopausal breast cancer with visceral metastases. Clin Breast Cancer. 2009 Feb;9(1):39-44. Fulvestrant and anastrozol (vs. AI) 1. 2. 3. Bergh J, Jönsson PE et al. FACT: An Open-Label Randomized Phase III Study of Fulvestrant and Anastrozole in Combination Compared With Anastrozole Alone As First-Line Therapy for Patients With Receptor-Positive Postmenopausal Breast Cancer. J Clin Oncol 30:1919-1925. 2012 Mehta RS, Barlow WE et al. Combination Anastrozole and Fulvestrant in Metastatic Breast Cancer. NEJM 367:43544, 2012 Johnston SR, Kilburn LS, Ellis P, Dodwell D, Cameron D, Hayward L, Im YH, Braybrooke JP, Brunt AM, Cheung KL, Jyothirmayi R, Robinson A, Wardley AM, Wheatley D, Howell A, Coombes G, Sergenson N, Sin HJ, Folkerd E, Dowsett M, Bliss JM; SoFEA investigators. Fulvestrant plus anastrozole or placebo versus exemestane alone after progression on non-steroidal aromatase inhibitors in postmenopausal patients with hormone-receptor-positive locally advanced or metastatic breast cancer (SoFEA): a composite, multicentre, phase 3 randomised trial. Lancet Oncol. 2013 Sep;14(10):989-98. Letrozole and Palbociclib (vs. Letrozol) 1. Finn RS, Crown JP, Lang I, Boer K, Bondarenko IM, Kulyk SO, Ettl J, Patel R, Pinter T, Schmidt M, Shparyk Y, Thummala AR, Voytko NL, Fowst C, Huang X, Kim ST, Randolph S, Slamon DJ. The cyclin-dependent kinase 4/6 inhibitor palbociclib in combination with letrozole versus letrozole alone as first-line treatment of oestrogen receptorpositive, HER2-negative, advanced breast cancer (PALOMA-1/TRIO-18): a randomised phase 2 study. Lancet Oncol. 2014 Dec 15. pii: S1470-2045(14)71159-3. 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Klijn JG, Blamey RW, Boccardo F, Tominaga T, Duchateau L, Sylvester R Combined tamoxifen and luteinizing hormone-releasing hormone (LHRH) agonist versus LHRH agonist alone in premenopausal advanced breast cancer: a meta-analysis of four randomized trials. J Clin Oncol. 2001 Jan 15;19(2):343-53. Boccardo F, Rubagotti A, Perrotta A, et al: Ovarian ablation versus goserelin with or without tamoxifen in preperimenopausal patients with advanced breast cancer: Results of a multicentric Italian study. Ann Oncol 5: 337-342, 1994 Ovarian function suppression (OFS), Tamoxifen 1. 2. 3. 4. 5. 6. 7. Taylor CW, Green S, Dalton WS, et al: Multicenter randomized clinical trial of goserelin versus surgical ovariectomy in premenopausal patients with receptor-positive metastatic breast cancer: an intergroup study. J Clin Oncol 1998;16:994999. Lees AW, Giuffre C, Burns PE, Hurlburt ME, Jenkins HJ: Oophorectomy versus radiation ablation of ovarian function in patients with metastatic carcinoma of the breast. Surg Gynecol Obstet 1980;151:721-724 Osborne CK: Tamoxifen in the treatment of breast cancer. N Engl J Med 1998;339:1609-1618 Ingle JN, Krook JE, Green SJ, et al: Randomized trial of bilateral oophorectomy versus tamoxifen in premenopausal women with metastatic breast cancer. J Clin Oncol 1986;4:178-185. Buchanan RB, Blamey RW, Durrant KR, et al: A randomized comparison of tamoxifen with surgical oophorectomy in premenopausal patients with advanced breast cancer. J Clin Oncol 1986;4:1326-1330. Sawka CA, Pritchard KI, Shelley W, et al: A randomized crossover trial of tamoxifen versus ovarian ablation for metastatic breast cancer in premenopausal women: a report of the National Cancer Institute of Canada Clinical Trials Group (NCIC CTG) trial MA.1. Breast Cancer Res Treat 1997;44:211-215. 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