Contemporary outcomes of metastatic breast cancer among 22,000 women from the multicentre ESME cohort 2008-2016.
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Deluche Elise, Antoine Alison, Bachelot Thomas, Lardy-Cleaud Audrey, Dieras Veronique, Brain Etienne, Debled Marc, Jacot William, Mouret-Reynier Marie Ange, Goncalves Anthony, Dalenc Florence, Patsouris Anne, Ferrero Jean Marc, Levy Christelle, Lorgis Veronique, Vanlemmens Laurence, Lefeuvre-Plesse Claudia, Mathoulin-Pelissier Simone, Petit Thierry, Uwer Lionel, Jouannaud Christelle, Leheurteur Marianne, Lacroix-Triki Magali, Courtinard Coralie, Perol David, Robain Mathieu, Delaloge Suzette
Аннотация
METHODS: Women aged ≥18 years with newly diagnosed MBC and who initiated MBC treatment between January 2008 and December 2016 in one of the 18 French Comprehensive Cancer Centers (N = 22,109) were included. We assessed the full patients' characteristics, first-line treatments, overall survival (OS) and first-line progression-free survival, as well as updated prognostic factors in the whole cohort and among the 3 major subtypes: hormone receptor positive and HER2-negative (HR+/HER2-, n = 13,656), HER2-positive (HER2+, n = 4017) and triple-negative (n = 2963) tumours.
RESULTS: The median OS of the whole cohort was 39.5 months (95% confidence interval [CI], 38.7-40.3). Five-year OS was 33.8%. OS differed significantly between the 3 subtypes (p < 0.0001) with a median OS of 43.3 (95% CI, 42.5-44.5) in HR+/HER2-; 50.1 (95% CI, 47.6-53.1) in HER2+; and 14.8 months (95% CI, 14.1-15.5) in triple-negative subgroups, respectively. Beyond performance status, the following variables had a constant significant negative prognostic impact on OS in the whole cohort and among subtypes: older age at diagnosis of metastases (except for the triple-negative subtype), metastasis-free interval between 6 and 24 months, presence of visceral metastases and number of metastatic sites ≥ 3.
CONCLUSIONS: The ESME program represents a unique large-scale real-life cohort on MBC. This study highlights important situations of high medical need within MBC patients. DATABASE REGISTRATION: clinicaltrials.gov Identifier NCT032753.