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  3. Peptide receptor radionuclide therapy for patients with somatostatin receptor expressing tumours. German Guideline (S1).
 

Peptide receptor radionuclide therapy for patients with somatostatin receptor expressing tumours. German Guideline (S1).

Peptidrezeptor-Radionuklidtherapie Somatostatinrezeptor- exprimierender Tumore. DGN-Leitlinie (S1)

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BORIS DOI
10.7892/boris.67180
Date of Publication
February 16, 2015
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
Poeppel, T D
Boy, Christian
Universitätsklinik für Nuklearmedizin
Bockisch, A
Kotzerke, J
Buchmann, I
Ezziddin, S
Scheidhauer, K
Krause, B J
Schmidt, D
Amthauer, H
Rösch, F
Nagarajah, J
Führer, D
Lahner, H
Pöpperl, G
Hörsch, D
Walter, Martin Alexanderorcid-logo
Universitätsklinik für Nuklearmedizin
Baum, R P
Subject(s)

600 - Technology::610...

Series
Nuklearmedizin / Nuclear medicine
ISSN or ISBN (if monograph)
0029-5566
Publisher
Schattauer
Language
German
PubMed ID
25683107
Uncontrolled Keywords

DOTATATE

DOTATOC

NEN

NET

Neuroendocrine tumour...

PRRT

guideline

peptide receptor radi...

Description
This document describes the guideline for peptide receptor radionuclide therapy (PRRT) published by the German Society of Nuclear Medicine (DGN) and accepted by the Association of the Scientific Medical Societies in Germany (AWMF) to be included in the official AWMF Guideline Registry. These recommendations are a prerequisite for the quality management in the treatment of patients with somatostatin receptor expressing tumours using PRRT. They are aimed at guiding nuclear medicine specialists in selecting likely candidates to receive PRRT and to deliver the treatment in a safe and effective manner. The recommendations are based on an interdisciplinary consensus. The document contains background information and definitions and covers the rationale, indications and contraindications for PRRT. Essential topics are the requirements for institutions performing the therapy, e. g. presence of an expert for medical physics, intense cooperation with all colleagues involved in the treatment of a patient, and a certificate of instruction in radiochemical labelling and quality control are required. Furthermore, it is specified which patient data have to be available prior to performance of therapy and how treatment has to be carried out technically. Here, quality control and documentation of labelling are of great importance. After treatment, clinical quality control is mandatory (work-up of therapy data and follow-up of patients). Essential elements of follow-up are specified in detail. The complete treatment inclusive after-care has to be realised in close cooperation with the involved medical disciplines. Generally, the decision for PRRT should be undertaken within the framework of a multi-disciplinary tumour board.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/132182
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Peptid-Rezeptor-Radionuklid-Therapie (PRRT) Somatostatin Rezeptor exprimierender Tumore_WAL.pdftextAdobe PDF202.12 KBpublished
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