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

Sandro Barni

*Author for correspondence: Tel.: +39 0363 424223; Fax: +39 0363 424380;

E-mail Address: sandro_barni@asst-bgovest.it

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

,
Luca Livraghi

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

,
Maria Morritti

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

,
Patrizia Vici

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

,
Andrea Michelotti

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

,
Saverio Cinieri

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

,
Caterina Fontanella

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

,
Luca Porcu

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

,
Lucia Del Mastro

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

,
Fabio Puglisi

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

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

&
Published Online:https://doi.org/10.2217/fon-2018-0324

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.

Papers of special note have been highlighted as: • of interest; •• of considerable interest

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