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Cumulative incidence of cardiovascular events under tamoxifen and letrozole alone and in sequence: a report from the BIG 1-98 trial.
Rabaglio, Manuela; Sun, Zhuoxin; Maibach, Rudolf; Giobbie-Hurder, Anita; Ejlertsen, Bent; Harvey, Vernon J; Neven, Patrick; Láng, István; Bonnefoi, Hervé; Wardley, Andrew; Ruepp, Barbara; Castiglione, Monica; Coates, Alan S; Gelber, Richard D; Goldhirsch, Aron; Colleoni, Marco; Thürlimann, Beat; Regan, Meredith M.
Afiliação
  • Rabaglio M; International Breast Cancer Study Group (IBCSG) Coordinating Center, Bern, Switzerland. manuela.rabaglio@insel.ch.
  • Sun Z; Department of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland. manuela.rabaglio@insel.ch.
  • Maibach R; Swiss Group for Clinical Cancer Research (SAKK), Bern, Switzerland. manuela.rabaglio@insel.ch.
  • Giobbie-Hurder A; Division of Biostatistics, IBCSG Statistical Center, Dana-Farber Cancer Institute, 450 Brookline Ave, Boston, MA, 02215, USA.
  • Ejlertsen B; International Breast Cancer Study Group (IBCSG) Coordinating Center, Bern, Switzerland.
  • Harvey VJ; Division of Biostatistics, IBCSG Statistical Center, Dana-Farber Cancer Institute, 450 Brookline Ave, Boston, MA, 02215, USA.
  • Neven P; Danish Breast Cancer Cooperative Group, Copenhagen, Denmark.
  • Láng I; Department of Oncology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • Bonnefoi H; Breast Cancer Trials (Formerly Known As the Breast Cancer Institute of Australia & Australia and New Zealand Breast Cancer Trials Group, Auckland City Hospital, Auckland, New Zealand.
  • Wardley A; Gynecologic Oncology and Multidisciplinary Breast Center, University Hospitals UZ-Leuven, KU Leuven, Leuven, Belgium.
  • Ruepp B; Istenhegyi Géndiagnosztika Private Health Center, Oncology Clinic, Budapest, Hungary.
  • Castiglione M; Institut Bergonié Unicancer, Université de Bordeaux, Bordeaux, France.
  • Coates AS; NIHR Manchester Clinical Research Facility At The Christie and Division of Cancer Sciences, Manchester Academic Health Science Center, University of Manchester, Manchester, UK.
  • Gelber RD; International Breast Cancer Study Group (IBCSG) Coordinating Center, Bern, Switzerland.
  • Goldhirsch A; International Breast Cancer Study Group (IBCSG) Coordinating Center, Bern, Switzerland.
  • Colleoni M; Swiss Group for Clinical Cancer Research (SAKK), Bern, Switzerland.
  • Thürlimann B; International Breast Cancer Study Group (IBCSG) Coordinating Center, Bern, Switzerland.
  • Regan MM; University of Sydney, Sydney, Australia.
Breast Cancer Res Treat ; 185(3): 697-707, 2021 Feb.
Article em En | MEDLINE | ID: mdl-33159633
ABSTRACT

BACKGROUND:

Compared to tamoxifen, adjuvant treatment with aromatase inhibitors improves disease outcomes of postmenopausal women with hormone receptor-positive early breast cancer. In the international, randomized, double-blind BIG 1-98 trial, 8010 women were randomized to receive tamoxifen, letrozole, or sequential use of the agents for 5 years. With a focus on switching between agents, we investigated cardiovascular events over the entire 5-year treatment period.

METHODS:

Of the 6182 patients enrolled, 6144 started trial treatment and were included in this analysis. Adverse events occurring during study treatment until 30 days after cessation were considered. Eight cardiovascular event types were defined. Cumulative incidence of events were estimated using the Kaplan-Meier method, without consideration for competing events. Multivariable Cox models estimated hazard ratios (HR) with 95% confidence intervals (CI) for pairwise comparisons of treatment arms.

RESULTS:

While on study treatment, 6.5% of patients (n = 397) had any cardiac events reported; for 2.4%, the event was grades 3-5, of which 11 (0.2%) were grade 5. Letrozole monotherapy was associated with higher risk of grade 1-5 ischemic heart disease (HR = 1.81; 95% CI, 1.06-3.08) compared with tamoxifen monotherapy. Patients assigned sequential tamoxifen →letrozole (HR = 1.59; 95% CI, 0.92-2.74) or sequential letrozole → tamoxifen (HR = 1.20; 95% CI, 0.68-2.14) showed a lesser degree of risk elevation. Patients assigned to tamoxifen-containing regimens had significantly higher risk of grade 1-5 thromboembolic events (tamoxifen monotherapy HR = 2.10; 95% CI, 1.42-3.12; tamoxifen → letrozole HR = 1.96; 95% CI, 1.32-2.92; letrozole → tamoxifen HR = 1.56; 95% CI 1.03-2.35) as compared with patients assigned letrozole alone.

CONCLUSION:

When initiating or switching between adjuvant endocrine treatments in postmenopausal patients, age and medical history, with special attention to prior cardiovascular events, should be balanced with expected benefit of the treatment.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Doenças Cardiovasculares Tipo de estudo: Clinical_trials / Incidence_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Doenças Cardiovasculares Tipo de estudo: Clinical_trials / Incidence_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article