Optimal management of luminal breast cancer: how much endocrine therapy is long enough?

被引:18
作者
Munzone, Elisabetta [1 ]
Colleoni, Marco [1 ]
机构
[1] European Inst Oncol, Div Med Senol, Via Ripamonti 435, I-20141 Milan, Italy
关键词
aromatase inhibitor; breast cancer; gene-expression profiling; hormone receptor-positive breast cancer; hormone therapy; luminal breast cancer; molecular testing; tamoxifen; EXTENDED ADJUVANT LETROZOLE; LATE DISTANT RECURRENCE; ANNUAL HAZARD RATES; POSTMENOPAUSAL WOMEN; RANDOMIZED-TRIAL; TAMOXIFEN THERAPY; OVARIAN SUPPRESSION; COST-EFFECTIVENESS; UPDATED FINDINGS; RISK;
D O I
10.1177/1758835918777437
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patients with early estrogen receptor-positive breast cancer are at continuous risk of relapse even after more than 10 years of follow up. Currently, no biomarker that identifies patients for early versus late recurrence, or one that selects patients or tumors for longer versus shorter durations of endocrine therapy (ET) is available and a crucial question is how to properly select patients who could be spared extended ET or those who require it. In the last 20 years more than 40,000 women were enrolled in randomized trials to answer the question of optimal duration of ET. According to the results of these studies extended adjuvant ET is more effective than standard 5 years of adjuvant ET. Extended ET in patients who remain premenopausal after 5 years of adjuvant tamoxifen is still tamoxifen for another 5 years. Extended ET with aromatase inhibitors (AIs) should be offered to postmenopausal women with substantial residual risk of relapse after completing 5 years of tamoxifen therapy. Extension of AI treatment to 10 years resulted in significantly better 5-year disease-free survival including disease recurrence local/distant or the occurrence of contralateral breast cancer events. Currently, new therapeutic targets are under investigation, but the beneficial effect of prolonged treatment for high-risk patients, identified by using multigenomic tests, remains unclear. Thus, further studies need to be performed to confirm the advantage of extended adjuvant ET in selected patients.
引用
收藏
页数:11
相关论文
共 48 条
[1]   Extended Adjuvant Tamoxifen for Early Breast Cancer: A Meta-Analysis [J].
Al-Mubarak, Mustafa ;
Tibau, Ariadna ;
Templeton, Arnoud J. ;
Cescon, David W. ;
Ocana, Alberto ;
Seruga, Bostjan ;
Amir, Eitan .
PLOS ONE, 2014, 9 (02)
[2]   Toxicity of Adjuvant Endocrine Therapy in Postmenopausal Breast Cancer Patients: A Systematic Review and Meta-analysis [J].
Amir, Eitan ;
Seruga, Bostjan ;
Niraula, Saroj ;
Carlsson, Lindsay ;
Ocana, Alberto .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2011, 103 (17) :1299-1309
[3]  
[Anonymous], 2016 SAN ANT BREAST
[4]  
[Anonymous], 2017, 2017 SAN ANT BREAST
[5]  
[Anonymous], 2013, J CLIN ONCOL, V31, P5, DOI [10.1200/jco.2013.31.18_suppl.5, DOI 10.1200/JCO.2013.31.18_SUPPL.5, DOI 10.1200/JCO.2013.31.18SUPPL.5]
[6]   Optimal Duration of Extended Adjuvant Endocrine Therapy for Early Breast Cancer; Results of the IDEAL Trial (BOOG 2006-05) [J].
Blok, Erik J. ;
Kroep, Judith R. ;
Kranenbarg, Elma Meershoek-Klein ;
Duijm-de Carpentier, Marjolijn ;
Putter, Hein ;
van den Bosch, Joan ;
Maartense, Eduard ;
van Leeuwen-Stok, A. Elise ;
Liefers, Gerrit-Jan ;
Nortier, Johan W. R. ;
Rutgers, Emiel J. Th. ;
van de Velde, Cornelis J. H. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2018, 110 (01) :40-48
[7]   Treatment Adherence and Its Impact on Disease-Free Survival in the Breast International Group 1-98 Trial of Tamoxifen and Letrozole, Alone and in Sequence [J].
Chirgwin, Jacquie H. ;
Giobbie-Hurder, Anita ;
Coates, Alan S. ;
Price, Karen N. ;
Ejlertsen, Bent ;
Debled, Marc ;
Gelber, Richard D. ;
Goldhirsch, Aron ;
Smith, Ian ;
Rabaglio, Manuela ;
Forbes, John F. ;
Neven, Patrick ;
Lang, Istvan ;
Colleoni, Marco ;
Thurlimann, Beat .
JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (21) :2452-+
[8]   Extended adjuvant intermittent letrozole versus continuous letrozole in postmenopausal women with breast cancer (SOLE): a multicentre, open-label, randomised, phase 3 trial [J].
Colleoni, Marco ;
Luo, Weixiu ;
Karlsson, Per ;
Chirgwin, Jacquie ;
Aebi, Stefan ;
Jerusalem, Guy ;
Neven, Patrick ;
Hitre, Erika ;
Graas, Marie-Pascale ;
Simoncini, Edda ;
Kamby, Claus ;
Thompson, Alastair ;
Loibl, Sibylle ;
Gavila, Joaquin ;
Kuroi, Katsumasa ;
Marth, Christian ;
Mueller, Bettina ;
O'Reilly, Seamus ;
Di Lauro, Vincenzo ;
Gombos, Andrea ;
Ruhstaller, Thomas ;
Burstein, Harold ;
Ribi, Karin ;
Bernhard, Jurg ;
Viale, Giuseppe ;
Maibach, Rudolf ;
Rabaglio-Poretti, Manuela ;
Gelber, Richard D. ;
Coates, Alan S. ;
Di Leo, Angelo ;
Regan, Meredith M. ;
Goldhirsch, Aron .
LANCET ONCOLOGY, 2018, 19 (01) :127-138
[9]   Annual Hazard Rates of Recurrence for Breast Cancer During 24 Years of Follow-Up: Results From the International Breast Cancer Study Group Trials I to V [J].
Colleoni, Marco ;
Sun, Zhuoxin ;
Price, Karen N. ;
Karlsson, Per ;
Forbes, John F. ;
Thurlimann, Beat ;
Gianni, Lorenzo ;
Castiglione, Monica ;
Gelber, Richard D. ;
Coates, Alan S. ;
Goldhirsch, Aron .
JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (09) :927-+
[10]   De-escalating and escalating treatments for early-stage breast cancer: the St. Gallen International Expert Consensus Conference on the Primary Therapy of Early Breast Cancer 2017 [J].
Curigliano, G. ;
Burstein, H. J. ;
Winer, E. P. ;
Gnant, M. ;
Dubsky, P. ;
Loibl, S. ;
Colleoni, M. ;
Regan, M. M. ;
Piccart-Gebhart, M. ;
Senn, H. -J. ;
Thurlimann, B. ;
Andre, F. ;
Baselga, J. ;
Bergh, J. ;
Bonnefoi, H. ;
Brucker, S. Y. ;
Cardoso, F. ;
Carey, L. ;
Ciruelos, E. ;
Cuzick, J. ;
Denkert, C. ;
Di Leo, A. ;
Ejlertsen, B. ;
Francis, P. ;
Galimberti, V. ;
Garber, J. ;
Gulluoglu, B. ;
Goodwin, P. ;
Harbeck, N. ;
Hayes, D. F. ;
Huang, C. -S. ;
Huober, J. ;
Khaled, H. ;
Jassem, J. ;
Jiang, Z. ;
Karlsson, P. ;
Morrow, M. ;
Orecchia, R. ;
Osborne, K. C. ;
Pagani, O. ;
Partridge, A. H. ;
Pritchard, K. ;
Ro, J. ;
Rutgers, E. J. T. ;
Sedlmayer, F. ;
Semiglazov, V. ;
Shao, Z. ;
Smith, I. ;
Toi, M. ;
Tutt, A. .
ANNALS OF ONCOLOGY, 2017, 28 (08) :1700-1712