New onset vasomotor symptoms but not musculoskeletal symptoms associate with clinical outcomes on extended adjuvant letrozole - Analyses from NCIC CTG MA.17

被引:5
作者
Liedke, P. E. R. [1 ,2 ,3 ,8 ]
Tu, D. [4 ]
Shepherd, L. [4 ]
Chavarri-Guerra, Y. [5 ,8 ]
Pritchard, K. I. [4 ,6 ]
Stearns, V. [7 ]
Goss, P. E. [4 ,8 ]
机构
[1] Hosp Clin Porto Alegre, Dept Clin Oncol, Porto Alegre, RS, Brazil
[2] Hosp Mae de Deus, Mae de Deus Canc Inst, Porto Alegre, RS, Brazil
[3] Brazilian Breast Canc Study Grp, Porto Alegre, RS, Brazil
[4] Queens Univ, Canadian Canc Trials Grp, Kingston, ON K7L 3N6, Canada
[5] Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Hematol Oncol, Salvador Zubiran, Mexico
[6] Univ Toronto, Sunnybrook Odette Canc Ctr, Toronto, ON, Canada
[7] Kimmel Canc Ctr Johns Hopkins, Breast Canc Program, Baltimore, MD USA
[8] Massachusetts Gen Hosp, Ctr Canc, Avon Int Breast Canc Res Program, Boston, MA 02114 USA
关键词
Breast cancer; Letrozole; Vasomotor symptoms; Musculoskeletal symptoms; Aromatase inhibitors; Extended hormonal therapy; BREAST-CANCER; RANDOMIZED-TRIAL; ADVERSE EVENTS; TAMOXIFEN; THERAPY; DISCONTINUATION; SURVIVAL; WOMEN;
D O I
10.1016/j.breast.2016.02.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: New onset symptoms on adjuvant aromatase inhibitors for hormone receptor positive early breast cancer may associate with clinical outcomes. We performed this exploratory analysis of the association of new onset musculoskeletal (MSK) and vasomotor (VM) symptoms with clinical outcomes in the NCIC CTG MA. 17 trial 5 years of extended adjuvant endocrine therapy with letrozole after tamoxifen. Methods: Symptoms were collected at baseline, 1, 6, and every 12 months on study. Multivariate Cox Models adjusting for age, nodal status, duration of tamoxifen and prior chemotherapy were used to compare disease-free survival (DFS), distant disease-free survival (DDFS), and overall survival (OS) based on data collected before, and after, the unblinding between women with VM or MSK symptoms and those without. Results: Data post-unblinding showed new VM symptoms on extended letrozole significantly improved DFS and DDFS when occurring 1 month (DFS HR 0.52, 95% CI, 0.28-0.96; p = 0.04; DDFS HR 0.49, 95% CI, 0.24-0.99; p = 0.046) and 6 months (DFS HR 0.43, 95% CI, 0.24-0.78; p = 0.006; DDFS HR 0.44, 95% CI, 0.22-0.85; p = 0.02) after treatment initiation. Those with new VM symptoms at 12 months also had a significantly better DFS (HR 0.47, 95% CI 0.26, 0.84; P = 0.01) and a trend in improved DDFS. Only a trend to improved OS was found for those with VM symptoms 6 month after treatment. No significant improvement was found for those with new MSK symptoms at any time point or for any endpoint. Conclusions: New onset VM symptoms with extended letrozole may be useful in predicting treatment benefit. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:99 / 104
页数:6
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