Switching to anastrozole versus continued tamoxifen treatment of early breast cancer: Preliminary results of the Italian Tamoxifen Anastrozole trial

被引:336
作者
Boccardo, F
Rubagotti, A
Puntoni, M
Guglielmini, P
Amoroso, D
Fini, A
Paladini, G
Mesiti, M
Romeo, D
Rinaldini, M
Scali, S
Porpiglia, M
Benedetto, C
Restuccia, N
Buzzi, F
Franchi, R
Massidda, B
Distante, V
Amadori, D
Sismondi, P
机构
[1] Ist Nazl Ric Canc, I-16132 Genoa, Italy
[2] Univ Genoa, I-16132 Genoa, Italy
[3] S Orsola M Malpighi Hosp, Bologna, Italy
[4] Univ Messina, Inst Oncol, Messina, Italy
[5] San Donato Hosp, Arezzo, Italy
[6] St Anna Hosp, Turin, Italy
[7] Univ Turin, Turin, Italy
[8] Molinette Mauriziano Hosp, Turin, Italy
[9] Inst Oncol S Luigi S Curro, Catania, Italy
[10] S Maria Hosp, Terni, Italy
[11] Civ Hosp, Casalpusterlengo, Italy
[12] Univ Cagliari, Cagliari, Italy
[13] Univ Florence, Florence, Italy
[14] Pierantoni Hosp, Forli, Italy
关键词
D O I
10.1200/JCO.2005.04.120
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Tamoxifen, which is actually the gold standard adjuvant treatment in estrogen receptor-positive early breast cancer, is associated with an increased risk of endometrial cancer and other life-threatening events. Moreover, many women relapse during or after tamoxifen therapy because of the development of resistance. Therefore new approaches are required. Patients and Methods We conducted a prospective randomized trial to test the efficacy of switching postmenopausal patients who were already receiving tamoxifen to the aromatase inhibitor anastrozole. After 2 to 3 years of tamoxifen treatment, patients were randomly assigned either to receive anastrozole 1 mg/d or to continue receiving tamoxifen 20 mg/d, for a total duration of treatment of 5 years. Disease-free survival was the primary end point. Event-free survival, overall survival, and safety were secondary end points. Results Four hundred forty-eight patients were enrolled. All women had node-positive, estrogen receptor-positive tumors. At a median follow-up time of 36 months, 45 events had been reported in the tamoxifen group compared with 17 events in the anastrozole group (P = .0002). Disease-free and local recurrence-free survival were also significantly longer in the anastrozole group (hazard ratio [HR] = 0.35; 95% CI, 0.18 to 0.68; P = .001 and HR = 0.15; 95% CI, 0.03 to 0.65; P = .003, respectively). Overall, more adverse events were recorded in the anastrozole group compared with the tamoxifen group (203 v 150, respectively; P = .04). However, more events were life threatening or required hospitalization in the tamoxifen group than in the anastrozole group (33 of 150 events v 28 of 203 events, P = .04). Conclusion Switching to anastrozole after the first 2 to 3 years of treatment is well tolerated and significantly improves event-free and recurrence-free survival in postmenopausal patients with early breast cancer.
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收藏
页码:5138 / 5147
页数:10
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