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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.
Afiliación
  • Tjan-Heijnen VCG; Division of Medical Oncology, GROW - School of Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, Netherlands. Electronic address: vcg.tjan.heijnen@mumc.nl.
  • van Hellemond IEG; Division of Medical Oncology, GROW - School of Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, Netherlands.
  • Peer PGM; Department for Health Evidence, Radboud Institute Health Sciences, Radboud University Medical Centre, Nijmegen, Netherlands.
  • Swinkels ACP; Clinical Research Department, Netherlands Comprehensive Cancer Organisation (IKNL), Nijmegen, Netherlands.
  • Smorenburg CH; Department of Medical Oncology, Antoni van Leeuwenhoek Hospital-Netherlands Cancer Institute, Amsterdam, Netherlands.
  • van der Sangen MJC; Department of Radiation Oncology, Catharina Hospital, Eindhoven, Netherlands.
  • Kroep JR; Department of Clinical Oncology, Leiden University Medical Center, Leiden, Netherlands.
  • De Graaf H; Department of Medical Oncology, Medical Centre Leeuwarden, Leeuwarden, Netherlands.
  • Honkoop AH; Department of Medical Oncology, Isala Clinics, Zwolle, Netherlands.
  • Erdkamp FLG; Department of Medical Oncology, Zuyderland Medical Center Heerlen-Sittard-Geleen, Sittard-Geleen, Geleen, Netherlands.
  • van den Berkmortel FWPJ; Department of Medical Oncology, Zuyderland Medical Center Heerlen-Sittard-Geleen, Heerlen, Netherlands.
  • de Boer M; Division of Medical Oncology, GROW - School of Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, Netherlands.
  • de Roos WK; Department of Surgery, Gelderse Vallei Hospital, Ede, Netherlands.
  • Linn SC; Department of Medical Oncology, Netherlands Cancer Institute, Amsterdam, Netherlands; Department of Pathology, University Medical Centre Utrecht, Netherlands.
  • Imholz ALT; Department of Medical Oncology, Deventer Hospital, Deventer, Netherlands.
  • Seynaeve CM; Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, Netherlands.
Lancet Oncol ; 18(11): 1502-1511, 2017 11.
Article en En | MEDLINE | ID: mdl-29031778
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. 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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tamoxifeno / Triazoles / Neoplasias de la Mama / Antineoplásicos Hormonales / Inhibidores de la Aromatasa / Nitrilos Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Adult / Aged / Female / Humans / Middle aged País/Región como asunto: Europa Idioma: En Revista: Lancet Oncol Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tamoxifeno / Triazoles / Neoplasias de la Mama / Antineoplásicos Hormonales / Inhibidores de la Aromatasa / Nitrilos Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Adult / Aged / Female / Humans / Middle aged País/Región como asunto: Europa Idioma: En Revista: Lancet Oncol Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article