Optimising Radioligand Therapy for Patients with Gastro-Entero-Pancreatic Neuroendocrine Tumours: Expert Opinion from an Italian Multidisciplinary Group
- PMID: 37987917
- PMCID: PMC10796590
- DOI: 10.1007/s12325-023-02714-8
Optimising Radioligand Therapy for Patients with Gastro-Entero-Pancreatic Neuroendocrine Tumours: Expert Opinion from an Italian Multidisciplinary Group
Abstract
Radioligand therapy (RLT) with lutetium (177Lu) oxodotreotide is an approved therapy in combination with somatostatin analogues (SSAs) for patients with advanced, well-differentiated G1-G2, gastro-entero-pancreatic neuroendocrine tumours (GEP-NETs) that progress on SSAs. We conducted a series of round table meetings throughout Italy to identify issues related to RLT delivery to patients with GEP-NETs. Four key issues were identified: (1) the proper definition of tumour progression prior to RLT initiation; (2) the impact of RLT in patients with bone metastases and/or high hepatic tumour burden; (3) the optimal follow-up protocol after RLT; and (4) organisational issues related to RLT use and managerial implications. This article reviews the literature relating to the aforementioned issues and makes recommendations based on available evidence and Italian NET experts' opinions. In particular, the group recommends the development of a diagnostic-therapeutic care pathway (DTCP) for patients undergoing RLT which provides systematic guidance but can still be individualised for each patient's clinical and psychosocial needs. A DTCP may clarify the diagnostic, therapeutic and post-treatment monitoring process, and improve communication and the coordination of care between hub and spoke centres. The DTCP may also contribute to changes in the care process related to the 2013/59/EURATOM Directive and to the definition of costs when planning for future or updated reimbursement of RLT in Italy.
Keywords: Diagnostic–therapeutic care pathway; Expert opinion; Gastro-entero-pancreatic neuroendocrine tumours; Italy; Lutetium (177Lu) oxodotreotide; Organizational implications, radioligand therapy.
© 2023. The Author(s).
Conflict of interest statement
Nicola Fazio has received fees for public speaking and advisory board activities from Novartis, Advanced Accelerator Applications, Ipsen, Sanofi, Hutchmed, Merck and MSD. Mirco Bartolomei has received fees for advisory board activities from Advanced Accelerator Applications. Diego Ferone has received fees for public speaking and advisory board activities from Advanced Accelerator Applications, Ipsen, Sandoz, Recordati and Camurus. Emanuela Foglia has received educational grants and advisory boards fees from Advanced Accelerator Applications, Ethicon, Astellas Pharma and Werfen—Instrumentation Laboratories. Franco Grimaldi has received fees from Advanced Accelerator Applications, Novo Nordisk, Boehringer Ingelheim, Ipsen, Merck, Eisai and Roche. Marco Volante has received fees for advisory board activities from Advanced Accelerator Applications. Secondo Lastoria has received fees for advisory board activities from Advanced Accelerator Applications. Massimo Falconi, Alfredo Berruti, Mirko D’Onofrio, Alessandro Giordano, Massimo Milione, Francesco Panzuto, Monica Santimaria, Orazio Schillaci, Ettore Seregni, and Michele Stasi declare that they have no competing interests.
References
-
- European Medicines Agency. Summary of product characteristics - Lutathera. 2017. European Medicines Agency. https://www.ema.europa.eu/en/documents/product-information/lutathera-epa.... Accessed 29 Apr 2022.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous
