Semi-automatic Segmentation Method for Determining 177Lu-DOTATATE Tumor Dosimetry
NCT ID: NCT06460467
Last Updated: 2025-03-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
25 participants
OBSERVATIONAL
2024-11-01
2025-02-28
Brief Summary
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Detailed Description
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Nevertheless, these recommendations are precise as regards dosimetry to organs at risk, but remain unclear as regards tumor dosimetry. Tumor dosimetry is therefore difficult to implement on a routine clinical basis.
The efficacy of 177Lu-DOTATATE treatment has been demonstrated for neuroendocrine tumors in the NETTER-1 phase 3 study, and interesting results have been reported for the treatment of refractory meningiomas.
Furthermore, a recent study showed that in patients with gastrointestinal neuroendocrine tumors treated with 177Lu-DOTATATE, tumor dosimetry could predict patient survival.
In order to optimize a dosimetric approach in clinical routine, several steps are necessary: i) define a standardized manual or semi-automated segmentation method for determining the volumes of interest (tumor volume and/or organs at risk), ii) precisely quantify tumor or organs at risk volume activities over time, and iii) determine the doses absorbed by the tumor and/or organs at risk.
An initial study was conducted in the department of nuclear medicine,to define a semi-automatic segmentation method for meningiomas treated with 177Lu-DOTATATE on pre-therapeutic 68Ga-DOTATOC positons emission tomography (PET), with the aim of predicting tumor dosimetry from pretherapeutic imaging. For this study, tumor segmentation will be performed directly on SPECT imaging carried out post-treatment on a 360° wide-field CZT camera to determine tumor dosimetry.
The aim of this study is to compare a semi-automatic segmentation method with manual reference segmentation to determine overall tumor volume on post-therapy scintigraphy at D1 in patients treated with 177Lu-DOTATATE for meningioma or neuroendocrine tumor, with a view to dosimetric calculation.
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Patients treated with 177Lu-DOTATATE
Patients treated with 177Lu-DOTATATE for a meningioma at the Nancy University Hospital and for a neuroencrine tumor in the EVADOVE study NCT04467567 (who underwent scintigraphy on D1, D4 and D7 (± 1 day)
scintigraphy of 177Lu-DOTATATE
The medical device under study is a hybrid wide-field CZT solid-state camera, the VERITON-CT ™ camera.
Interventions
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scintigraphy of 177Lu-DOTATATE
The medical device under study is a hybrid wide-field CZT solid-state camera, the VERITON-CT ™ camera.
Eligibility Criteria
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Inclusion Criteria
* Patients with neuroendocrine tumors in the EVADOV study who underwent scintigraphy on D1, D4 and D7 (± 1 day)
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Central Hospital, Nancy, France
OTHER
Responsible Party
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BOURSIER Caroline
Principal Investigator
Locations
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Nuclear medicine Department CHRU de NANCY
Vandœuvre-lès-Nancy, , France
Countries
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Other Identifiers
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2024PI103
Identifier Type: -
Identifier Source: org_study_id
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