Extended adjuvant aromatase inhibition after sequential endocrine therapy (DATA): a randomised, phase 3 trial
Tjan-Heijnen, Vivianne C G; van Hellemond, Irene E G; Peer, Petronella G M; Swinkels, Astrid C P; Smorenburg, Carolien H; van der Sangen, Maurice J C; Kroep, Judith R; De Graaf, Hiltje; Honkoop, Aafke H; Erdkamp, Frans L G; van den Berkmortel, Franchette W P J; de Boer, Maaike; de Roos, Wilfred K; Linn, Sabine C; Imholz, Alexander L T; Seynaeve, Caroline M; Dutch Breast Cancer Research Group (BOOG) for the DATA Investigators
(2017) LANCET ONCOLOGY, volume 18, issue 11, pp. 1502 - 1511
(Article)
Abstract
Background The effect of extended adjuvant aromatase inhibition in hormone receptor-positive breast cancer after sequential endocrine therapy of tamoxifen followed by an aromatase inhibitor for a 5-year treatment period still needs clarification. To address this issue, we began the DATA study to assess different durations of anastrozole therapy after tamoxifen.
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Methods DATA was a prospective, randomised, open-label, multicentre, phase 3 study done in 79 hospitals in the Netherlands. We randomly assigned postmenopausal women with hormone receptor-positive early breast cancer with no signs of disease recurrence after 2–3 years of adjuvant tamoxifen to either 3 or 6 years of anastrozole treatment (1 mg orally once a day) in a 1:1 ratio. We used TENALEA (Trans European Network for Clinical Trials Services) for the randomisation procedure. Stratification factors were nodal status, hormone receptor status, HER2 status, and tamoxifen treatment duration. The primary study endpoint of this analysis was disease-free survival starting beyond 3 years after randomisation (adapted disease-free survival). Here we report the final analysis from the DATA trial, which is registered with ClinicalTrials.gov, number NCT00301457. Findings Between June 28, 2006, and Aug 10, 2009, we screened 1912 patients of whom 955 were assigned to the 3-year group and 957 to the 6-year anastrozole treatment group. 1860 patients were eligible (931 in the 6-year group and 929 in the 3-year group) and 1660 were disease free 3 years after randomisation. The 5-year adapted disease-free survival was 83·1% (95% CI 80·0–86·3) in the 6-year group and 79·4% (76·1–82·8) in the 3-year group (hazard ratio [HR] 0·79 [95% CI 0·62–1·02]; p=0·066). Patients in the 6-year treatment group had more adverse events than those in the 3-year treatment group, including all-grade arthralgia or myalgia (478 [58%] of 827 in the 6-year treatment group vs 438 [53%] of 833 in the 3-year treatment group) and osteopenia or osteoporosis (173 [21%] vs 137 [16%]). Interpretation We cannot recommend the use of extended adjuvant aromatase inhibition after 5 years of sequential endocrine therapy in all postmenopausal women with hormone receptor-positive breast cancer. Funding AstraZeneca.
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Keywords: Administration, Oral, Adult, Aged, Antineoplastic Agents, Hormonal, Aromatase Inhibitors, Breast Neoplasms, Chemotherapy, Adjuvant, Disease-Free Survival, Dose-Response Relationship, Drug, Drug Administration Schedule, Female, Humans, Kaplan-Meier Estimate, Mastectomy, Maximum Tolerated Dose, Middle Aged, Netherlands, Nitriles, Postmenopause, Prognosis, Prospective Studies, Receptor, ErbB-2, Survival Analysis, Tamoxifen, Treatment Outcome, Triazoles, Clinical Trial, Phase III, Comparative Study, Multicenter Study, Randomized Controlled Trial, Oncology
ISSN: 1470-2045
Publisher: Lancet Publishing Group
Note: Funding Information: Development of the study design was supported by the Dutch Breast Cancer Research Group (BOOG), led by VCGT-H, IEGvH, PGMP, and ACPS. The study was supported and completed through the Netherlands Comprehensive Cancer Organisation (IKNL), Nijmegen, Netherlands. PGMP was responsible for the detailed statistical analysis. VCGT-H, IEGvH, PGMP, and ACPS interpreted the data and prepared the initial draft of the report; they also collated changes proposed by all of the authors into the final draft paper before final approval by all of the named coauthors. All authors gave final approval of the version to be published. Publisher Copyright: © 2017 Elsevier Ltd
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