| Literature DB >> 35884396 |
Alexander Heinzel1,2,3, Daniela Dedic1, Norbert Galldiks2,3,4, Philipp Lohmann2,5, Gabriele Stoffels2, Christian P Filss1,2,3, Martin Kocher2,3,5, Filippo Migliorini6, Kim N H Dillen7, Stefanie Geisler2, Carina Stegmayr2, Antje Willuweit2, Michael Sabel3,8, Marion Rapp3,8, Michael J Eble3,9, Marc Piroth10, Hans Clusmann3,11, Daniel Delev3,11, Elena K Bauer3,4, Garry Ceccon3,4, Veronika Dunkl3,4, Jurij Rosen3,4, Caroline Tscherpel3,4, Jan-Michael Werner3,4, Maximilian I Ruge3,5, Roland Goldbrunner3,12, Jürgen Hampl3,12, Carolin Weiss Lucas3,12, Ulrich Herrlinger3,13, Gabriele D Maurer14, Joachim P Steinbach14, Jörg Mauler2, Wieland A Worthoff2, Bernd N Neumaier2,15, Christoph Lerche2, Gereon R Fink2,3,4, Nadim Jon Shah2,16,17, Felix M Mottaghy1,3,18, Karl-Josef Langen1,2,3,16.
Abstract
O-(2-[18F]fluoroethyl)-L-tyrosine (FET) is a widely used amino acid tracer for positron emission tomography (PET) imaging of brain tumours. This retrospective study and survey aimed to analyse our extensive database regarding the development of FET PET investigations, indications, and the referring physicians' rating concerning the role of FET PET in the clinical decision-making process. Between 2006 and 2019, we performed 6534 FET PET scans on 3928 different patients against a backdrop of growing demand for FET PET. In 2019, indications for the use of FET PET were as follows: suspected recurrent glioma (46%), unclear brain lesions (20%), treatment monitoring (19%), and suspected recurrent brain metastasis (13%). The referring physicians were neurosurgeons (60%), neurologists (19%), radiation oncologists (11%), general oncologists (3%), and other physicians (7%). Most patients travelled 50 to 75 km, but 9% travelled more than 200 km. The role of FET PET in decision-making in clinical practice was evaluated by a questionnaire consisting of 30 questions, which was filled out by 23 referring physicians with long experience in FET PET. Fifty to seventy per cent rated FET PET as being important for different aspects of the assessment of newly diagnosed gliomas, including differential diagnosis, delineation of tumour extent for biopsy guidance, and treatment planning such as surgery or radiotherapy, 95% for the diagnosis of recurrent glioma, and 68% for the diagnosis of recurrent brain metastases. Approximately 50% of the referring physicians rated FET PET as necessary for treatment monitoring in patients with glioma or brain metastases. All referring physicians stated that the availability of FET PET is essential and that it should be approved for routine use. Although the present analysis is limited by the fact that only physicians who frequently referred patients for FET PET participated in the survey, the results confirm the high relevance of FET PET in the clinical diagnosis of brain tumours and support the need for its approval for routine use.Entities:
Keywords: O-(2-[18F]fluoroethyl)-L-tyrosine (FET); amino acid PET; brain metastasis; brain tumour diagnosis; glioma; positron emission tomography
Year: 2022 PMID: 35884396 PMCID: PMC9319157 DOI: 10.3390/cancers14143336
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.575
Figure 1Number of FET PET investigations at the FZJ since 2001.
Figure 2Fraction of indications in 2019.
Referrers’ rating of the significance of FET PET for different indications.
| Indication. | Very Important or Important |
|---|---|
|
| |
| Confirmation of suspected glioma | 50% |
| Extent of glioma | 59% |
| Biopsy guidance | 64% |
| OP/RTX planning | 73% |
|
| |
| Tumour residuals (yes/no) | 41% |
| Estimation of tumour extent | 45% |
|
| |
| Suspected recurrence (yes/no) | 95% |
| Detection of pseudoprogression/radionecrosis | 95% |
| Extent of the recurrent tumour | 95% |
| Planning of surgery/radiotherapy | 91% |
|
| |
| Temozolomide | 55% |
| PCV scheme | 55% |
| Antiangiogenic therapy | 55% |
| Immunotherapy | 50% |
| Other therapies | 53% |
|
| |
| Suspected recurrence (yes/no) | 68% |
| Therapy monitoring | 50% |
“Very important or important” = Rating <3 according to a rating scale ranging from 1, very important, to 5, unimportant. Right column: percentage of referrers rating <3.
Referrers’ rating of the percentage of patients in which FET PET is necessary for different indications.
| Indication | Mean ± SD (%) | FET PET Necessary in |
|---|---|---|
| Differential diagnosis of brain lesion | 47 ± 31% | 55% |
| Prognosis of gliomas | 43 ± 28% | 55% |
| Biopsy guidance in gliomas | 50 ± 30% | 64% |
| Tumour extent for OP/RT planning | 54 ± 24% | 75% |
| Diagnosis of recurrent gliomas | 68 ± 22% | 91% |
| Therapy monitoring in gliomas | 53 ± 27% | 73% |
| Diagnosis of recurrent brain metastasis | 45 ± 31% | 45% |
| Therapy monitoring of brain metastasis | 36 ± 29% | 36% |
Rating of the referrers regarding the necessity of FET PET in different indications in five steps: <10%; 25%, 50%, 75% and >90% of patients. Right column: percentage of referrers rating FET PET as necessary in ≥ 50% of the patients.
Rating of the significance of advanced MR procedures (PWI, MRS, and DWI) for different indications compared to FET PET.
| Indication | Adv. MRI Very Important or Important |
|---|---|
| Differential diagnosis of brain lesion | 52% |
| Diagnosis of recurrent gliomas | 57% |
| Therapy monitoring in gliomas | 52% |
| Diagnosis of recurrent brain metastasis | 52% |
| Therapy monitoring of brain metastasis | 38% |
“Very important or important” = Rating <3 according to a rating scale ranging from 1, very important, to 5, unimportant. Right column: percentage of referrers’ rating <3.
Referrers’ rating on the general availability of FET PET.
| Statement | Correct |
|---|---|
| The availability of FET PET is very important for me | 100% |
| The availability of FET PET is sufficient for my needs | 86% |
| FET PET should be approved as a standard procedure | 100% |
| FET PET should be available in specialised neuro-oncological centres only | 86% |
“Correct” = Rating <3 according to a rating scale ranging from 1, correct, to 5, not correct. Right column: percentage of referrers rating <3.