Evidence map›Paper›PMID 41193909›Full record

ReviewEJNMMI reports2025

Molecular imaging in the diagnostic process of neuroendocrine tumors: a systematic review on unknown primary origin and suspected NETs.

Laura Alonzo, Roberto Cannella, Riccardo Laudicella, Viviana Benfante, Pierpaolo Purpura, Giuseppe Micci, Massimo Galia, Giuseppe Brancatelli, Massimo Midiri, Pierpaolo Alongi

Abstract readReview
In one paragraph

Review in EJNMMI reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Laura AlonzoDepartment of Radiology, AOUP Paolo Giaccone, Via del Vespro 129, Palermo, 90127, Italy.
Roberto CannellaDepartment of Radiology, AOUP Paolo Giaccone, Via del Vespro 129, Palermo, 90127, Italy.
Riccardo LaudicellaNuclear Medicine, Department of Biomedical and Dental Sciences and Morpho-Functional Imaging, Messina University, Messina, Italy.
Viviana BenfanteAdvanced Diagnostic Imaging-INNOVA Project, Department of Radiological Sciences, A.R.N.A.S. Civico Di Cristina e Benfratelli Hospitals, Palermo, Italy.
Pierpaolo PurpuraAdvanced Diagnostic Imaging-INNOVA Project, Department of Radiological Sciences, A.R.N.A.S. Civico Di Cristina e Benfratelli Hospitals, Palermo, Italy.
Giuseppe MicciDepartment of Radiology, AOUP Paolo Giaccone, Via del Vespro 129, Palermo, 90127, Italy.
Massimo GaliaDepartment of Radiology, AOUP Paolo Giaccone, Via del Vespro 129, Palermo, 90127, Italy.
Giuseppe BrancatelliDepartment of Radiology, AOUP Paolo Giaccone, Via del Vespro 129, Palermo, 90127, Italy.
Massimo MidiriDepartment of Biomedicine, Neuroscience and Advanced Diagnostics (BiND), University of Palermo, Palermo, 90127, Italy.
Pierpaolo AlongiDepartment of Biomedicine, Neuroscience and Advanced Diagnostics (BiND), University of Palermo, Palermo, 90127, Italy. alongi.pierpaolo@gmail.com.ORCID http://orcid.org/0000-0002-8397-1640

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeuroendocrine tumors (NETs) are a heterogeneous group of neoplasms often arising in the gastrointestinal tract, pancreas, and lungs. Diagnosing NETs can be challenging due to their small size, slow growth, and low metabolic activity, especially in cases of unknown primary origin (CUP-NETs). Timely identification of the primary lesion is critical for tailored treatment planning, including peptide receptor radionuclide therapy (PRRT), surgery, or somatostatin analogue administration.

objectiveThis systematic review evaluates the diagnostic performance and clinical impact of molecular imaging-especially PET/CT with radiolabeled somatostatin analogs-in patients with suspected NETs or CUP-NETs.

methodsFollowing PRISMA guidelines, a comprehensive literature search was conducted in PubMed and Scopus. Data on study design, tracers used, detection rates, and impact on patient management were extracted. Quality assessment was performed using CASP tools.

resultsPET/CT using [68 Ga]Ga-DOTA-peptides (DOTATATE, DOTATOC, DOTANOC) consistently outperformed conventional SPECT imaging with [111In]Pentetreotide (Octreoscan), achieving primary tumor detection rates of 38%-83% versus < 10% with SPECT. In suspected NETs, PET/CT demonstrated high sensitivity (up to 95%) and specificity ( > 85%), with changes in clinical management reported in up to 33% of cases. Dual-tracer imaging ([68 Ga]Ga-DOTATATE and [18F]FDG) and newer tracers such as [18F]DOPA and [18F]AlF-NOTA-octreotide ([18F]-OC) provided added diagnostic value, particularly in aggressive or rare subtypes (e.g. paragangliomas, insulinomas). Detection of unknown primaries commonly led to curative surgical options or more targeted therapies.

conclusionsMolecular imaging-particularly [

Indexed as

CUPDota-peptidesNeuroendocrine tumorPositron-emission-tomographySingle photon emission tomographySomatostatine receptorUPO

Identifiers

PMID41193909
PMCPMC12589696

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.