Biganzoli, Laura http://orcid.org/0000-0001-7989-8658
Cinieri, Saverio
Berardi, Rossana
Pedersini, Rebecca
McCartney, Amelia
Minisini, Alessandro Marco
Caremoli, Elena Rota
Spazzapan, Simon
Magnolfi, Emanuela
Brunello, Antonella
Risi, Emanuela
Palumbo, Raffaella
Leo, Silvana
Colleoni, Marco
Donati, Sara
De Placido, Sabino
Orlando, Laura
Pistelli, Mirco
Parolin, Veronica
Mislang, Anna
Becheri, Dimitri
Puglisi, Fabio
Sanna, Giuseppina
Zafarana, Elena
Boni, Luca
Mottino, Giuseppe
Funding for this research was provided by:
Celgene (IIT29673)
Article History
Received: 20 February 2020
Accepted: 22 July 2020
First Online: 5 August 2020
Ethics approval and consent to participate
: The study was conducted in accordance with the principles of the Declaration of Helsinki and Good Clinical Practice Guidelines of the Internal Conference on Harmonisation. The protocol and any accompanying material provided to patients were prospectively approved by the local independent ethics committee at each of the 15 participating sites.
: Not applicable.
: DB has received honoraria from Pfizer, Daiichi Sankyo, and MDM and research funding from Daiichi Sankyo. RB has undertaken a consulting or advisory role with Otsuka and Boeringher. LBi has received honoraria from Lilly, Novartis, and Pfizer; has undertaken a consulting or advisory role with AstraZeneca, Celgene, Daiichi-Sankyo, Eisai, Genomic Health, Ipsen, Lilly, Novartis, Pfizer, Pierre Fabre, and Roche; has received research funding (institutional) from Celgene, Genomic Health, and Novartis; and has received travel, accommodation, or expenses from Celgene, Pfizer, Ipsen, and Roche.AB has undertaken a consulting or advisory role with Eisai, Roche, and Eli Lilly and has received research funding from Roche and travel, accommodations, or expenses from Eli Lilly and Pharmamar. SC has undertaken a consulting or advisory role with Lilly. MC has received honoraria from Novartis and has undertaken a consulting or advisory role with Pierre Fabre, Pfizer, OBI Pharma, Puma Biotechnology, Celldex, and AstraZeneca. SDP has received honoraria from Roche, Celgene, GSK, Novartis, Ipsen, and AstraZeneca; has undertaken a consulting or advisory role with Roche, Celgene, GSK, Novartis, Ipsen, Lilly, Pfizer, and AstraZeneca; has served on speaker’s bureau with Roche, Novartis, Lilly, Pfizer, AstraZeneca, Celgene, Eisai, and Istituto Gentili; has received research funding from Eisai, Novartis, Roche; and AstraZeneca, and travel, accommodation; and expenses from Roche, GSK, Novartis, Liilly, Pfizer, Eisai, and AstraZeneca. SD has received travel, accommodation, or expenses from Roche, Novartis, and Takeda. AMM has undertaken a consulting or advisory role with Novartis, Merck Sharp & Dohme, and Pierre Fabre. MP has received honoraria from Celgene, Novartis, Pfizer, and Istituto Gentili; has undertaken a consulting or advisory role with Novartis and Sandoz; and received travel, accommodation, or expenses from Celgene and Istituto Gentili. FP has received honoraria from Amgen, Eli Lilly, Ipsen, Merck Sharp & Dohme, Roche, and Takeda; has undertaken a consulting or advisory role with Eisai, Eli Lilly, Novartis, Pfizer, Pierre Fabre, and Roche; has received research funding from AstraZeneca, Eisai, and Roche; and received travel, accommodation, or expenses from Celgene and Roche. ER has received travel, accommodation, or expenses from Pfizer. GS has received honoraria from Novartis, has undertaken a consulting or advisory role with Roche, and has received travel, accommodation, or expenses from Eisai, Novartis, Pfizer, Pierre Fabre, and Roche. SS has received honoraria from Pfizer and Novartis; has undertaken a consulting or advisory role with Novartis and has received research funding (institution) from Roche, Novartis, and Abbott, and travel, accommodations or expenses from Pfizer, Istituto Gentili, and Tesaro. All remaining authors declare that they have no competing interests.