Eribulin in the treatment of advanced breast cancer: real-world scenario from 39 Italian centers – ESEMPiO study

Author:

Barni Sandro1,Livraghi Luca2,Morritti Maria3,Vici Patrizia4,Michelotti Andrea5,Cinieri Saverio6,Fontanella Caterina7,Porcu Luca8,Del Mastro Lucia9,Puglisi Fabio710,

Affiliation:

1. Oncology Unit, Medical Department, ASST Bergamo Ovest, 24047, Treviglio, Italy

2. Medical Oncology Unit, ASST Papa Giovanni XXIII, 24127, Bergamo, Italy

3. Oncology Unit, Ospedale Casa Sollievo della Sofferenza, 71013, San Giovanni Rotondo, Foggia, Italy

4. Division of Medical Oncology 2, “Regina Elena” National Cancer Institute, 00128, Rome, Italy

5. Oncology Unit 1, Azienda Ospedaliera Universitaria Pisana, 56126, Pisa, Italy

6. Medical Oncology Division and Breast Unit, “Senatore Antonio Perrino” Hospital, 72100, Brindisi, Italy

7. Unit of Medical Oncology and Cancer Prevention, IRCCS Centro di Riferimento Oncologico Aviano-National Cancer Institute, 33081, Aviano, Italy

8. Laboratory of Methodology for Clinical Research, Oncology Department, IRCCS – Istituto di Ricerche Farmacologiche Mario Negri,  20156, Milan, Italy

9. Department of Internal Medicine, University of Genova, Ospedale Policlinico San Martino, 16132, Genoa, Italy

10. Medical Oncology, Department of Medicine, University of Udine, 33100, Udine, Italy

Abstract

Aim: We performed a multicenter retrospective cohort study of eribulin mesylate (EM) use in Italy, to describe the current practice for metastatic breast cancer patients (ESEMPiO) in the real-world. Patients & methods: Baseline characteristics, treatment administration and safety were summarized using descriptive statistics. Results: No safety concerns were raised in the population enrolled in the ESEMPiO database and treated in a real-life practice. Median progression-free survival and overall survival were 3.2 and 10.1 months, respectively. EM activity was similar between breast cancer subtypes. Conclusion: In metastatic breast cancer patients treated with EM in ‘real-world’ setting, the clinician-registered outcomes were comparable to those reported in pivotal trials. Furthermore, EM maintained clinical activity and a tolerable safety profile.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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