医学
来曲唑
乳腺癌
内科学
临床终点
三苯氧胺
随机对照试验
肿瘤科
人口
芳香化酶抑制剂
背景(考古学)
意向治疗分析
辅助治疗
癌症
外科
古生物学
环境卫生
生物
作者
Lucia Del Mastro,Mauro Mansutti,Giancarlo Bisagni,Riccardo Ponzone,Antonio Durando,Laura Amaducci,Enrico Campadelli,F. Cognetti,Antonio Frassoldati,Andrea Michelotti,Silvia Mura,Ylenia Urracci,Giovanni Sanna,Stefania Gori,Sabino De Placido,Ornella Garrone,Alessandra Fabi,C. Barone,Stefano Tamberi,Claudia Bighin,Fabio Puglisi,Gabriella Moretti,Grazia Arpino,Alberto Ballestrero,Francesca Poggio,Matteo Lambertini,Filippo Montemurro,Paolo Bruzzi
出处
期刊:Lancet Oncology
[Elsevier]
日期:2021-09-17
卷期号:22 (10): 1458-1467
被引量:52
标识
DOI:10.1016/s1470-2045(21)00352-1
摘要
Summary
Background
The benefit of extending aromatase inhibitor therapy beyond 5 years in the context of previous aromatase inhibitors remains controversial. We aimed to compare extended therapy with letrozole for 5 years versus the standard duration of 2–3 years of letrozole in postmenopausal patients with breast cancer who have already received 2–3 years of tamoxifen. Methods
This multicentre, open-label, randomised, phase 3 trial was done at 69 hospitals in Italy. Women were eligible if they were postmenopausal at the time of study entry, had stage I–III histologically proven and operable invasive hormone receptor-positive breast cancer, had received adjuvant tamoxifen therapy for at least 2 years but no longer than 3 years and 3 months, had no signs of disease recurrence, and had an Eastern Cooperative Oncology Group performance status of 2 or lower. Patients were randomly assigned (1:1) to receive 2–3 years (control group) or 5 years (extended group) of letrozole (2·5 mg orally once a day). Randomisation, with stratification by centre, with permuted blocks of size 12, was done with a centralised, interactive, internet-based system that randomly generated the treatment allocation. Participants and investigators were not masked to treatment assignment. The primary endpoint was invasive disease-free survival in the intention-to-treat population. Safety analysis was done for patients who received at least 1 month of study treatment. This trial was registered with EudraCT, 2005-001212-44, and ClinicalTrials.gov, NCT01064635. Findings
Between Aug 1, 2005, and Oct 24, 2010, 2056 patients were enrolled and randomly assigned to receive letrozole for 2–3 years (n=1030; control group) or for 5 years (n=1026; extended group). After a median follow-up of 11·7 years (IQR 9·5–13·1), disease-free survival events occurred in 262 (25·4%) of 1030 patients in the control group and 212 (20·7%) of 1026 in the extended group. 12-year disease-free survival was 62% (95% CI 57–66) in the control group and 67% (62–71) in the extended group (hazard ratio 0·78, 95% CI 0·65–0·93; p=0·0064). The most common grade 3 and 4 adverse events were arthralgia (22 [2·2%] of 983 patients in the control group vs 29 [3·0%] of 977 in the extended group) and myalgia (seven [0·7%] vs nine [0·9%]). There were three (0·3%) serious treatment-related adverse events in the control group and eight (0·8%) in the extended group. No deaths related to toxic effects were observed. Interpretation
In postmenopausal patients with breast cancer who received 2–3 years of tamoxifen, extended treatment with 5 years of letrozole resulted in a significant improvement in disease-free survival compared with the standard 2–3 years of letrozole. Sequential endocrine therapy with tamoxifen for 2–3 years followed by letrozole for 5 years should be considered as one of the optimal standard endocrine treatments for postmenopausal patients with hormone receptor-positive breast cancer. Funding
Novartis and the Italian Ministry of Health. Translation
For the Italian translation of the abstract see Supplementary Materials section.