Position Statement on the Diagnosis, Treatment, and Response Evaluation to Systemic Therapies of Advanced Neuroendocrine Tumors, With a Special Focus on Radioligand Therapy.

advanced neoadjuvant therapy neuroendocrine tumors peptide receptor radionuclide therapy progression retreatment sequencing

Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
05 04 2022
Historique:
received: 15 06 2021
accepted: 08 10 2021
entrez: 5 4 2022
pubmed: 6 4 2022
medline: 8 4 2022
Statut: ppublish

Résumé

The aim of this study was to provide a guidance for the management of neuroendocrine tumors (NETs) in clinical practice. Nominal group and Delphi techniques were used. A steering committee of 8 experts reviewed the current management of NETs, identified controversies and gaps, critically analyzed the available evidence, and formulated several guiding statements for clinicians. Subsequently, a panel of 26 experts, was selected to test agreement with the statements through 2 Delphi rounds. Items were scored on a 4-point Likert scale from 1 = totally agree to 4 = totally disagree. The agreement was considered if ≥75% of answers pertained to Categories 1 and 2 (consensus with the agreement) or Categories 3 and 4 (consensus with the disagreement). Overall, 132 statements were proposed, which incorporated the following areas: (1) overarching principles; (2) progression and treatment response criteria; (3) advanced gastro-enteric NETs; (4) advanced pancreatic NETs; (5) advanced NETs in other locations; (6) re-treatment with radioligand therapy (RLT); (7) neoadjuvant therapy. After 2 Delphi rounds, only 4 statements lacked a clear consensus. RLT was not only recommended in the sequencing of different NETs but also as neoadjuvant treatment, while several indications for retreatment with RLT were also established. This document sought to pull together the experts' attitudes when dealing with different clinical scenarios of patients suffering from NETs, with RLT having a specific role where evidence-based data are limited.

Sections du résumé

BACKGROUND
The aim of this study was to provide a guidance for the management of neuroendocrine tumors (NETs) in clinical practice.
MATERIAL AND METHODS
Nominal group and Delphi techniques were used. A steering committee of 8 experts reviewed the current management of NETs, identified controversies and gaps, critically analyzed the available evidence, and formulated several guiding statements for clinicians. Subsequently, a panel of 26 experts, was selected to test agreement with the statements through 2 Delphi rounds. Items were scored on a 4-point Likert scale from 1 = totally agree to 4 = totally disagree. The agreement was considered if ≥75% of answers pertained to Categories 1 and 2 (consensus with the agreement) or Categories 3 and 4 (consensus with the disagreement).
RESULTS
Overall, 132 statements were proposed, which incorporated the following areas: (1) overarching principles; (2) progression and treatment response criteria; (3) advanced gastro-enteric NETs; (4) advanced pancreatic NETs; (5) advanced NETs in other locations; (6) re-treatment with radioligand therapy (RLT); (7) neoadjuvant therapy. After 2 Delphi rounds, only 4 statements lacked a clear consensus. RLT was not only recommended in the sequencing of different NETs but also as neoadjuvant treatment, while several indications for retreatment with RLT were also established.
CONCLUSION
This document sought to pull together the experts' attitudes when dealing with different clinical scenarios of patients suffering from NETs, with RLT having a specific role where evidence-based data are limited.

Identifiants

pubmed: 35380724
pii: 6543669
doi: 10.1093/oncolo/oyab041
pmc: PMC8982404
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e328-e339

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press.

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Auteurs

Jaume Capdevila (J)

Department of Medical Oncology, Vall Hebron University Hospital, Vall Hebron Institute of Oncology (VHIO), IOB-Quiron-Teknon Barcelona, Barcelona, Spain.

Enrique Grande (E)

Department of Medical Oncology, MD Anderson Cancer Center, Madrid, Spain.

Rocío García-Carbonero (R)

Department of Medical Oncology, Hospital Universitario Doce de Octubre, Madrid, Spain.

Marc Simó (M)

Department of Nuclear Medicine and Molecular Imaging, Hospital Universitari Vall d'Hebron, Barcelona, Spain.

Mª Isabel Del Olmo-García (MI)

Department of Endocrinology, Hospital Universitario y Politécnico la Fe de Valencia, Valencia, Spain.

Paula Jiménez-Fonseca (P)

Department of Medical Oncology, Hospital Universitario Central de Asturias, ISPA, Madrid, Spain.

Alberto Carmona-Bayonas (A)

Department of Hematology and Medical Oncology, Hospital General Universitario Morales Meseguer, University of Murcia, IMIB, CP13/00126, PI17/0050 (ISCIII & FEDER) and Fundación Séneca (04515/GERM/06), Murcia, Spain.

Virginia Pubul (V)

Department of Nuclear Medicine Department and Molecular Imaging Research Group, University Hospital and Health Research Institute of Santiago de Compostela (IDIS), Santiago de Compostela, Spain.

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