Evidence map›Paper›PMID 42387196›Full record

ArticleEJNMMI research2026

Automatic lesion segmentation in ⁶⁸Ga-PSMA PET/CT and ¹⁷⁷Lu-PSMA SPECT/CT: added value of PET-guided SPECT in a bicentric study.

Solène Perret, Léa Albe, Agathe Edet-Sanson, David Tonnelet, Thomas Carlier, Camilla Kohi, Matthieu Barbaud, Romain Modzelewski, Pierre Vera, Laetitia Augusto and 5 more

Abstract read
In one paragraph

Article in EJNMMI research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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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

1 citing paper in PubMed.

  1. 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

15 authors.

Solène PerretQuantIF AIMS, University of Rouen, Rouen, France. solene.perret-neveux@chb.unicancer.fr.ORCID http://orcid.org/0009-0002-1908-2571
Léa AlbeNuclear Medicine Department, Henri Becquerel Cancer Centre, Rouen, France.
Agathe Edet-SansonQuantIF AIMS, University of Rouen, Rouen, France.
David TonneletNuclear Medicine Department, Henri Becquerel Cancer Centre, Rouen, France.
Thomas CarlierNuclear Medicine Department, Nantes University Hospital, Nantes, France.
Camilla KohiNuclear Medicine Department, Nantes University Hospital, Nantes, France.
Matthieu BarbaudNuclear Medicine Department, Nantes University Hospital, Nantes, France.
Romain ModzelewskiQuantIF AIMS, University of Rouen, Rouen, France.
Pierre VeraQuantIF AIMS, University of Rouen, Rouen, France.
Laetitia AugustoHepatogastroenterology Department, Rouen University Hospital, Rouen, France.
Frédéric Di FioreHepatogastroenterology Department, Rouen University Hospital, Rouen, France.
Sébastien HapdeyQuantIF AIMS, University of Rouen, Rouen, France.
Clément BaillyNuclear Medicine Department, Nantes University Hospital, Nantes, France.
Arnaud DieudonnéQuantIF AIMS, University of Rouen, Rouen, France.
Pierre DecazesQuantIF AIMS, University of Rouen, Rouen, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundManual segmentation of prostate cancer metastases on PSMA PET/CT and SPECT/CT is time-consuming and poorly scalable, particularly in highly metastatic patients. This study evaluated nnU-Net-based automatic segmentation models trained on PET and SPECT either separately or jointly and assessed whether PET-derived information can improve SPECT lesion segmentation. Seventy-three patients with metastatic castration-resistant prostate cancer treated with ¹⁷⁷Lu-PSMA were retrospectively included: 48 from the Henri Becquerel Cancer Center (HBCC) and 25 from Nantes University Hospital (NUH). For each patient, ⁶⁸Ga-PSMA PET/CT and ¹⁷⁷Lu-PSMA SPECT/CT were acquired before and during the first treatment cycle respectively. All images were manually segmented by four nuclear medicine physicians in consensus. Four nnU-Net models were trained: M1 (PET/CT only), M2 (SPECT/CT only), M3 (joint PET/CT+SPECT/CT, unimodal input at inference), and M4 (SPECT/CT with PET/CT segmentation as a priori input). Models were first trained and internally validated on HBCC data, then retrained on the full HBCC cohort and externally validated on NUH data.

resultsFor PET/CT segmentation, M1 and M3 achieved comparable performance. M1 reached DSCs of 0.83 ± 0.19 (internal) and 0.76 ± 0.22 (external), while M3 achieved 0.83 ± 0.16 (internal) and 0.77 ± 0.21 (external). For SPECT/CT, the PET-guided model M4 (DSC: 0.63 ± 0.24 internal; 0.78 ± 0.14 external; PPV: 0.65 ± 0.26 internal; 0.75 ± 0.23 external) provided the best results. Compared with the SPECT-only model M2 (DSC: 0.61 ± 0.26 internal; 0.70 ± 0.25 external; PPV: 0.63 ± 0.25 internal; 0.71 ± 0.24 external), M4 showed no statistically significant difference in internal validation (DSC p = 0.35), while being statistically significant in external validation (DSC p = 0.014).

conclusionThe nnU-Net framework enables accurate lesion segmentation on both ⁶⁸Ga-PSMA PET/CT and ¹⁷⁷Lu-PSMA SPECT/CT. While PET-only and joint PET+SPECT models perform similarly on PET images, incorporating PET-derived segmentations as prior information tends to improve SPECT/CT lesion segmentation. This PET-guided SPECT segmentation strategy leverages the higher spatial resolution of PET and represents a key step towards fully automated extraction of volumetric and dosimetric biomarkers for personalized prostate cancer treatment.

Indexed as

Automatic lesion segmentationDeep learningPositron emission tomography (PET)Prostate-specific membrane antigen (PSMA)Prostatic adenocarcinomaSingle-photon emission tomography (SPECT)

Identifiers

PMID42387196
PMCPMC13593981

What Socratic holds

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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 Socratic graph.