Time trends of overall survival among metastatic breast cancer patients in the real-life ESME cohort

被引:212
|
作者
Gobbini, Elisa [1 ]
Ezzalfani, Monia [2 ]
Dieras, Veronique [3 ,4 ]
Bachelot, Thomas [5 ]
Brain, Etienne [3 ,4 ]
Debled, Marc [6 ]
Jacot, William [7 ]
Mouret-Reynier, Marie Ange [8 ]
Goncalves, Anthony [9 ]
Dalenc, Florence [10 ]
Patsouris, Anne [11 ]
Ferrero, Jean Marc [12 ]
Levy, Christelle [13 ]
Lorgis, Veronique [14 ]
Vanlemmens, Laurence [15 ]
Lefeuvre-Plesse, Claudia [16 ]
Mathoulin-Pelissier, Simone [17 ]
Petit, Thierry [18 ]
Uwer, Lionel [19 ]
Jouannaud, Christelle [20 ]
Leheurteur, Marianne [21 ]
Lacroix-Triki, Magali [22 ]
Cleaud, Audrey Lardy [2 ]
Robain, Mathieu [23 ]
Courtinard, Coralie [23 ]
Cailliot, Christian [23 ]
Perol, David [2 ]
Delaloge, Suzette [1 ]
机构
[1] Gustave Roussy, Dept Canc Med, 114 Rue Edouard Vaillant, F-94800 Villejuif, France
[2] Ctr Leon Berard, Dept Biostat, 28 Promenade Lea & Napoleon Bullukian, F-69008 Lyon, France
[3] Inst Curie, Dept Med Oncol, 26 Rue DUlm, F-75005 Paris, France
[4] Inst Curie, Dept Med Oncol, St Cloud, France
[5] Ctr Leon Berard, Dept Med Oncol, 28 Prom Lea & Napoleon Bullukian, F-69008 Lyon, France
[6] Inst Bergonie, Dept Med Oncol, 229 Cours LArgonne, F-33000 Bordeaux, France
[7] Inst Canc Montpellier, Dept Med Oncol, 208 Rue Apothicaires, F-34298 Montpellier, France
[8] Ctr Jean Perrin, Dept Med Oncol, 58 Rue Montalembert, F-63011 Clermont Ferrand, France
[9] Inst Paoli Calmettes, Dept Med Oncol, 232 Blvd St Marguerite, F-13009 Marseille, France
[10] Inst Claudius Regaud IUCT Oncopole, Dept Med Oncol, 1 Ave Irene Joliot Curie, F-31059 Toulouse, France
[11] Inst Cancerol Ouest Nantes & Angers, Dept Med Oncol, 15 Rue Andre Boquel, F-49055 Angers, France
[12] Ctr Antoine Lacassagne, Dept Med Oncol, 33 Ave Valambrose, F-06189 Nice, France
[13] Ctr Francois Baclesse, Dept Med Oncol, 3 Ave Gen Harris, F-14000 Caen, France
[14] Ctr Georges Francois Leclerc, Dept Med Oncol, 1 Rue Prof Marion, F-21079 Dijon, France
[15] Ctr Oscar Lambret, Dept Med Oncol, 3 Rue Frederic Combemale, F-59000 Lille, France
[16] Ctr Eugene Marquis, Dept Med Oncol, Ave Bataille Flandres Dunkerque, F-35000 Rennes, France
[17] Inst Bergonie, INSERM CIC1401, Ctr Comprehens Canc, F-33000 Bordeaux, France
[18] Ctr Paul Strauss, Dept Med Oncol, 3 Rue Porte Hop, F-67000 Strasbourg, France
[19] Inst Cancerol Jean Godinot, Dept Med Oncol, 1 Rue Gen Koenig, F-51100 Reims, France
[20] Inst Cancerol Lorraine, Dept Med Oncol, 6 Ave Bourgogne, F-54519 Vandoeuvre Les Nancy, France
[21] Ctr Henri Becquerel, Dept Med Oncol, Rue Amiens, F-76000 Rouen, France
[22] Gustave Roussy, Dept BioPathol, 114 Rue Edouard Vaillant, F-94800 Villejuif, France
[23] R&D Unicanc, Dept Res & Dev, 101 Rue Tolbiac, F-75654 Paris, France
关键词
Metastatic breast cancer; Overall survival; Subtypes; HER2; POSTMENOPAUSAL WOMEN; ENDOCRINE THERAPY; PHYSICIANS CHOICE; 1ST-LINE THERAPY; FOLLOW-UP; TRASTUZUMAB; FULVESTRANT; COMBINATION; TRIAL; ANASTROZOLE;
D O I
10.1016/j.ejca.2018.03.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: Real-life analysis of overall survival (OS) trends among metastatic breast cancer (MBC) patients may help define medical needs and evaluate the impact of public health investments. The present study aimed to evaluate the independent impact of the year of MBC diagnosis on OS in the Epidemio-Strategy-Medical-Economical (ESME)-MBC cohort. Methods: ESME-MBC (NCT03275311) is a French, national, multicentre, observational cohort including 16,702 consecutive newly diagnosed MBC patients (01 January 2008-31 December 2014). Of 16,680 eligible patients, 15,085 had full immunohistochemistry data, allowing classification as hormone receptor-positive and HER2-negative (HR+/HER2-, N=9907), HER2-positive (HER2+, N=2861) or triple-negative (HR-/HER2-, N=2317) subcohorts. Multivariate analyses of OS were conducted among the full ESME cohort and subcohorts. Results: Median OS of the whole cohort was 37.22 months (95% confidence interval [CI], 36.3-38.04). Year of diagnosis was an independent predictor of OS (hazard ratio 0.98 [95% CI, 0.97-1.00], P=.01) together with age, subtype, disease-free interval, visceral metastases and number of organs involved. Median OS of HR+/HER2-, HER2+ and HR-/HER2- subcohorts was, respectively, 42.12 (95% CI, 40.90-43.10), 44.91 (95% CI, 42.51-47.90) and 14.52 (95% CI, 13.70-15.24) months. Year of diagnosis was a strong independent predictor of OS in HER2+ subcohort (hazard ratio 0.91 [95% CI, 0.88-0.94], P<.001), but not in HR+/HER2- nor HR-/HER2- subcohorts (hazard ratio 1.00 [95% CI, 0.98-1.01], P .80 and 1.00 [95% CI, 0.97-1.02], P .90, respectively). Conclusions: The OS of MBC patients has slightly improved over the past decade. However, this effect is confined to HER2+ cases, highlighting the need of new strategies in the other subtypes. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:17 / 24
页数:8
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