5-year follow-up of a randomized controlled trial of immediate versus delayed zoledronic acid for the prevention of bone loss in postmenopausal women with breast cancer starting letrozole after tamoxifen: N03CC (Alliance) trial

被引:25
作者
Wagner-Johnston, Nina D. [1 ]
Sloan, Jeff A. [2 ]
Liu, Heshan [2 ]
Kearns, Ann E. [3 ]
Hines, Stephanie L. [4 ]
Puttabasavaiah, Suneetha [2 ]
Dakhil, Shaker R. [5 ]
Lafky, Jacqueline M. [3 ]
Perez, Edith A. [4 ]
Loprinzi, Charles L. [3 ]
机构
[1] Washington Univ, Sch Med, Div Med Oncol, St Louis, MO 63110 USA
[2] Mayo Clin, Alliance Stat & Data Ctr, Rochester, MN USA
[3] Mayo Clin, Div Med Oncol, Rochester, MN USA
[4] Mayo Clin Florida, Dept Hematol Oncol, Jacksonville, FL USA
[5] Wichita Community Clin Oncol Program, Wichita, KS USA
关键词
zoledronic acid; bone loss; postmenopausal; breast cancer; letrozole; tamoxifen; ADJUVANT THERAPY; MINERAL DENSITY; ZO-FAST; METAANALYSIS; COMBINATION;
D O I
10.1002/cncr.29327
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUNDPostmenopausal women with breast cancer receiving aromatase inhibitors are at an increased risk of bone loss. The current study was undertaken to determine whether upfront versus delayed treatment with zoledronic acid (ZA) impacted bone loss. This report described the 5-year follow-up results. METHODSA total of 551 postmenopausal women with breast cancer who completed tamoxifen treatment and were undergoing daily letrozole treatment were randomized to either upfront (274 patients) or delayed (277 patients) ZA at a dose of 4 mg intravenously every 6 months. In the patients on the delayed treatment arm, ZA was initiated for a postbaseline bone mineral density T-score of <-2.0 or fracture. RESULTSThe incidence of a 5% decrease in the total lumbar spine bone mineral density at 5 years was 10.2% in the upfront treatment arm versus 41.2% in the delayed treatment arm (P<.0001). A total of 41 patients in the delayed treatment arm were eventually started on ZA. With the exception of increased NCI Common Toxicity Criteria (CTC) grade 1/2 elevated creatinine and fever in the patients treated on the upfront arm and cerebrovascular ischemia among those in the delayed treatment arm, there were no significant differences observed between arms with respect to the most common adverse events of arthralgia and back pain. Osteoporosis occurred less frequently in the upfront treatment arm (2 vs 8 cumulative cases), although this difference was not found to be statistically significant. Bone fractures occurred in 24 patients in the upfront treatment arm versus 25 patients in the delayed treatment arm. CONCLUSIONSImmediate treatment with ZA prevented bone loss compared with delayed treatment in postmenopausal women receiving letrozole and these differences were maintained at 5 years. The incidence of osteoporosis or fractures was not found to be significantly different between treatment arms. Cancer 2015;121:2537-2543. (c) 2015 American Cancer Society. At 5 years of follow-up of this randomized controlled trial, immediate treatment with ZA prevented bone loss compared with delayed treatment in postmenopausal women receiving letrozole for breast cancer. Differences between the treatment arms with regard to the development of osteoporosis or fractures were not statistically significant.
引用
收藏
页码:2537 / 2543
页数:7
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