Real-life activity of eribulin mesylate among metastatic breast cancer patients in the multicenter national observational ESME program

被引:32
作者
Jacot, William [1 ,2 ]
Heudel, Pierre-Etienne [3 ]
Fraisse, Julien [1 ]
Gourgou, Sophie [1 ]
Guiu, Severine [1 ,2 ]
Dalenc, Florence [4 ]
Pistilli, Barbara [5 ]
Campone, Mario [6 ]
Levy, Christelle [7 ]
Debled, Marc [8 ]
Leheurteur, Marianne [9 ]
Chaix, Marie [10 ]
Lefeuvre, Claudia [11 ]
Goncalves, Anthony [12 ]
Uwer, Lionel [13 ]
Ferrero, Jean-Marc [14 ]
Eymard, Jean-Christophe [15 ]
Petit, Thierry [16 ]
Mouret-Reynier, Marie-Ange [17 ]
Courtinard, Coralie [18 ]
Cottu, Paul [19 ]
Robain, Mathieu [18 ]
Mailliez, Audrey [20 ]
机构
[1] Montpellier Univ, Inst Canc Montpellier ICM Val dAurelle, Montpellier, France
[2] IRCM INSERM U1194, Montpellier, France
[3] Ctr Leon Berard, Lyon, France
[4] Inst Claudius Regaud, IUCT Oncopole, Toulouse, France
[5] Gustave Roussy, Villejuif, France
[6] Inst Cancerol Ouest, St Herblain, France
[7] Ctr Francois Baclesse, Caen, France
[8] Inst Bergonie, Bordeaux, France
[9] Ctr Henri Becquerel, Rouen, France
[10] Ctr Georges Francois Leclerc, Dijon, France
[11] Ctr Eugene Marquis, Rennes, France
[12] Inst Paoli Calmettes, Marseille, France
[13] Inst Cancerol Lorraine, Vandoeuvre Les Nancy, France
[14] Ctr Antoine Lacassagne, Nice, France
[15] Inst Cancerol Jean Godinot, Reims, France
[16] Ctr Paul Strauss, Strasbourg, France
[17] Ctr Jean Perrin, Clermont Ferrand, France
[18] UNICANCER, Paris, France
[19] Etab Hosp Inst Curie, Paris, France
[20] Ctr Oscar Lambret, Lille, France
关键词
metastatic breast cancer; eribulin; real-life cohort; PROGRESSION-FREE SURVIVAL; OPEN-LABEL; 1ST-LINE TREATMENT; LOCALLY RECURRENT; PLUS TRASTUZUMAB; SINGLE-ARM; PHASE-II; CHEMOTHERAPY; COMBINATION; THERAPY;
D O I
10.1002/ijc.32402
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Eribulin mesylate (EM) was recently approved for metastatic breast cancer (MBC) chemotherapy (CT) in late lines by the FDA, with debated results in second line. We evaluated outcomes in breast cancer patients receiving EM as second, third and fourth line in a national real-life cohort of 16,703 consecutive MBC patients initiating their first metastatic therapeutic line between 2008 and 2014. Primary and secondary objectives were overall survival (OS) and progression-free survival (PFS). An imbalance was seen for HER2+ tumors and concomitant anti-HER2 targeted therapies use, we thus performed a subanalysis in HER2- patients. PFS and OS were significantly better in EM patients in third and fourth lines, compared to "Other chemotherapies" patients (PFS: 4.14 vs. 3.02 months, p = 0.0010; 3.61 vs. 2.53 months, p = 0.0102, third and fourth-line; OS: 11.27 vs. 7.65 months, p = 0.0001; 10.91 vs. 5.95 months, p < 0.0001, third and fourth-line). No significant difference was reported in second-line (PFS: 5.06 vs. 4.14 months, p = 0.1171; OS: 13.99 vs. 11.66 months, p = 0.151). Among HER2- patients, a significant difference was seen for all lines, including 2nd-line (PFS: 4.57 vs. 3.91 months, p = 0.0379; OS: 14.98 vs. 10.51 months, p = 0.0113). In this large real-world database, HER2-negative MBC patients receiving EM in second or later CT line presented significantly better PFS and OS. This difference disappeared in second line in the overall population, probably because of the imbalance in HER2-targeted treatments use. Our results mirror those of the published randomized trials. The effect of anti-HER2 therapies addition in this setting still needs to be defined.
引用
收藏
页码:3359 / 3369
页数:11
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