Martínez-Ciarpaglini, Carolina
Barros, Rita
Caballero, Carmelo
Boggino, Hugo
Alarcón-Molero, Lorena
Peleteiro, Bárbara
Ruiz-García, Erika
Fernandez-Figueroa, Edith
Herrera-Goepfert, Roberto
Díaz-Romero, Consuelo
Ferreira, Rui
Groen-van Schooten, Tessa S.
Gauna, Cinthia
Pereira, Rita
Cantero, Daniel
Lezcano, Horacio
Esteso, Federico
O´Connor, Juan
Riquelme, Arnoldo
Owen, Gareth I.
Garrido, Marcelo
Roa, Juan Carlos
Ruiz-Pace, Fiorella
Vivancos, Ana
Diez-García, Marc
Alsina, Maria
Matito, Judit
Martin, Agatha
Gómez, Marina
Castillo, Ester
Vila, Maria
Santos-Antunes, João
Costa, Andreia
Lordick, Florian
Farrés, Judith
Palomar-De Lucas, Brenda
Cabeza-Segura, Manuel
Villagrasa, Rosanna
Jimenez-Martí, Elena
Miralles-Marco, Ana
Dienstmann, Rodrigo
Derks, Sarah
Figueiredo, Ceu
Cervantes, Andrés
Carneiro, Fátima
Fleitas-Kanonnikoff, Tania https://orcid.org/0000-0002-2789-9082
Funding for this research was provided by:
Horizon 2020 Framework Programme (GA825832)
conahcyt (297681)
ANID-FONDAP (152220002, 15130011)
Article History
Received: 24 August 2024
Accepted: 16 December 2024
First Online: 5 January 2025
Declarations
:
: Dr. Alsina discloses consultancy, advisory roles, honoraria from Amgen, AstraZeneca, Beigene, Drangofly Therapeutics, Jazz Pharmaceuticals, BMS, Lilly, Novartis and MSD. Institutional research funding from Merck. FL Dr. Lordick reports institutional grants from: Astra Zeneca, Beigene, BMS, Daiichi Sankyo and Gilead, and personal fees from: Amgen, ArtTempi. Astellas, Astra Zeneca, Bayer, Biontech, BMS, Boehringer Ingelheim, Daiichi Sankyo, Eli Lilly, Gilead, Elsevier, Incyte, Medscape, MedUpdate, Merck Serono, MSD, PAGE, Roche, Servier, StreamedUp!, VJ Oncology, all outside the submitted work. Dr. Fleitas discloses advisory roles honoraria from Amgen, AstraZeneca, Beigene, BMS and MSD. Institutional research funding from Gilead. Speaker honoraria from Amgen, Servier, BMS, MSD, Lilly, Roche, Bayer. The other authors has no conflict of interests to declare.
: The study has been conducted according to the principles of the Declaration of Helsinki (Fortaleza, Brazil, October 2013), following the Medical Research Involving Human Subjects Act and Good Clinical Practice standards. The study can be found under ClinicalTrials.gov Identifier: NCT04015466, July 11, 2019. The study protocol has been approved by the ethics committee of all patient-recruiting centers: the ethics committee of University Clinical Hospital of Valencia, Spain (reference number 2018/205), the institutional review board of VU University Medical Center Amsterdam (reference number 2019.355. NL 69480.02919), the ethics committee of Instituto de Previsión Social, Asuncion-Paraguay (reference number CA N°11–020/19), the ethical research committee of Instituto Alexander Fleming, Buenos Aires Argentina (Resolution July 25th, 2019, for LEGACy study 1 and 2 and October 3rd, 2019 for LEGACy study 3); the ethical committee of Instituto Nacional de Cancerología (INCAN, México (reference number INCAN/CEI/0486/19). The ethics committee of the University Center of Sao Joao and Medicine Faculty of Porto University, Portugal (reference 100/019), the scientific ethical Committee Pontificia University of Chili, reference 180806007, and the Drug research ethics committee of Valld’Hebron University Hospital, Barcelona, Spain with references PR (AG)387/2019 approved on October 29th, 2019 for LEGACy study 1, PR (AG)388/2019 approved in December 13th 2019 for LEGACy study 2 and PR (AG)419/2019 approved in January 30th, 2020 for Legacy study 3 respectively. All participants provided written informed consent before study enrolment. Each data-contributing partner has undergone online ethical and data training before the beginning of data collection and has managed access to the data of their center through this security system. Inside this system, a patient ID generator has generated a unique code for each participating patient to maintain data privacy.