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Real-life prognosis of 5041 bone-only metastatic breast cancer patients in the multicenter national observational ESME program.
Bertho, Marion; Fraisse, Julien; Patsouris, Anne; Cottu, Paul; Arnedos, Monica; Pérol, David; Jaffré, Anne; Goncalves, Anthony; Lebitasy, Marie-Paule; D'Hondt, Véronique; Dalenc, Florence; Ferrero, Jean-Marc; Levy, Christelle; Dabakuyo, Sandrine; Rouzier, Roman; Penault-Llorca, Frédérique; Uwer, Lionel; Eymard, Jean-Christophe; Breton, Mathias; Chevrot, Michaël; Thureau, Sébastien; Petit, Thierry; Simon, Gaëtane; Frénel, Jean-Sébastien.
Afiliação
  • Bertho M; Department of Medical Oncology, Institut de Cancérologie de l'Ouest - Paul Papin, Angers, France.
  • Fraisse J; Biometrics Unit, Regional Cancer Institute of Montpellier (ICM), Montpellier, France.
  • Patsouris A; Department of Medical Oncology, Institut de Cancérologie de l'Ouest - Paul Papin, Angers, France.
  • Cottu P; Department of Medical Oncology, Institut Curie, Paris, France.
  • Arnedos M; Department of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France.
  • Pérol D; Biostatistic Unit, Clinical Research and Innovation Department, Centre Léon Bérard, Lyon, France.
  • Jaffré A; Department of Medical Information, Institut Bergonié, Bordeaux, France.
  • Goncalves A; Department of Medical Oncology, Institut Paoli-Calmettes, Marseille, France.
  • Lebitasy MP; Clinical Research and Innovation Department, Centre Oscar Lambret, Lille, France.
  • D'Hondt V; Department of Medical Oncology, Institut du Cancer de Montpellier, Montpellier, France.
  • Dalenc F; Department of Medical Oncology, Institut Claudius Regaud, IUCT-Oncopole, Toulouse, France.
  • Ferrero JM; Department of Medical Oncology, Institut Centre Antoine Lacassagne, Nice, France.
  • Levy C; Department of Medical Oncology, Centre François Baclesse, Caen, France.
  • Dabakuyo S; National Quality of Life and Cancer Clinical Research Platform, Centre Georges François Leclerc, Dijon, France.
  • Rouzier R; Department of Surgical Oncology, Institut Curie, Saint-Cloud, France.
  • Penault-Llorca F; Department of Pathology and Molecular Pathology, Centre Jean Perrin, Clermont Ferrand, France.
  • Uwer L; Department of Medical Oncology, Institut de Cancérologie de Lorraine, Vandoeuvre-lès- Nancy, France.
  • Eymard JC; Department of Medical Oncology, Institut de Cancérologie Jean-Godinot, Reims, France.
  • Breton M; Department of Medical Information, Centre Eugène Marquis, Rennes, France.
  • Chevrot M; UNICANCER R&D, Paris, France.
  • Thureau S; Department of Radiation Oncology, Centre Henri Becquerel, Rouen, France.
  • Petit T; Department of Medical Oncology, Centre Paul Strauss, Strasbourg, France.
  • Simon G; UNICANCER R&D, Paris, France.
  • Frénel JS; Department of Medical Oncology, ICO René Gauducheau, Boulevard Jacques Monod, Saint Herblain, Pays de la Loire 44805, France.
Ther Adv Med Oncol ; 13: 1758835920987657, 2021.
Article em En | MEDLINE | ID: mdl-33613700
BACKGROUND: Bone-only (BO) metastatic breast cancer (MBC) is considered a more favorable entity than other MBC presentations. However, only few retrospective series and data from selected randomized controlled trials have been reported so far. METHODS: Using the French national multicenter ESME (Epidemiological Strategy and Medico Economics) Data Platform, the primary objective of our study was to compare the overall survival (OS) of patients with BO versus non-BO MBC at diagnosis, with adjustment on main prognostic factors using a propensity score. Secondary objectives were to compare first-line progression-free survival (PFS1), describe treatment patterns, and estimate factors associated with OS. RESULTS: Out of 20,095 eligible women, 5041 (22.4%) patients had BO disease [hormone-receptor positive (HR+)/human epidermal growth-factor-receptor-2 negative (HER2-), n = 4 102/13,229 (31%); HER2+, n = 644/3909 (16.5%); HR-/HER2-, n = 295/2 957 (10%)]. BO MBC patients had a better adjusted OS compared with non-BO MBC [52.1 months (95% confidence interval (CI) 50.3-54.1) versus 34.7 months (95% CI 34.0-35.6) respectively]. The 5-year OS rate of BO MBC patients was 43.4% (95% CI 41.7-45.2). They also had a better PFS1 [13.1 months (95% CI 12.6-13.8) versus 8.5 months (95% CI 8.3-8.7), respectively]. This observation could be repeated in all subtypes. BO disease was an independent prognostic factor of OS [hazard ratio 0.68 (95% CI 0.65-0.72), p < 0.0001]. Results were concordant in all analyses. CONCLUSION: BO MBC patients have better outcomes compared with non-BO MBC, consistently, through all MBC subtypes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article