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Unravelling Tumour Biology In Ovarian Cancer With Precision Imaging

Unravelling Tumour Biology In Ovarian Cancer With Precision Imaging

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06084195
Acronym
MR-O-MICS
Enrollment
120
Registered
2023-10-16
Start date
2023-12-19
Completion date
2029-10-31
Last updated
2025-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High Grade Serous Ovarian Cancer

Keywords

Radiomics, Ovarian cancer, Genomics, Proteomics, Immune Tumor Microenvironment

Brief summary

The objective of this study is to explore the integration of in vivo and ex vivo of MRI with histology and molecular assessments to advance non-invasive characterization of tumor heterogeneity in high-grade serous ovarian cance

Detailed description

After being informed about the study and potential risks, all patient giving wirtting informed consent. During surgery, tissue and blood samples will be conserved for the study. In this study will be compared images obtained in vivo before surgical management, ex vivo images obtained on excised tissues during surgery, histological data obtained during surgery.

Interventions

During the surgery : * Tissus sample : primary tumor and metastasis * blood sample : 3 EDTA tubes * ex vivo MRI data

Sponsors

Institut du Cancer de Montpellier - Val d'Aurelle
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient aged \>18 * Pathologically proven HGSOC at an advanced stage (FIGO IIIB or IIIC) which can benefit from surgery with or without prior neoadjuvant treatment * Willingness and ability to comply with planned visits, treatment plan, laboratory tests and other study procedures, * Patient who has given informed, written and express consent, * Patient affiliated with a French health insurance scheme.

Exclusion criteria

* Early-stage disease (FIGO \<IIIB) or presence of extraperitoneal metastases, * Patient who will not have surgery * Patient whose regular follow-up is impossible for psychological, family, social or geographical reasons, * Patient under guardianship, curatorship or safeguarding of justice, * Pregnant and/or nursing patient, * Patient with a history of other cancers within 5 years/10 years prior to inclusion

Design outcomes

Primary

MeasureTime frameDescription
the integration of in vivo and ex vivo of MRI with histology and molecular assessments to advance non-invasive characterization of tumor heterogeneity in high-grade serous ovarian cancer.one shoot at the surgeryThe diagnostic performance of the radiomic and multiomic algorithm for the characterization of heterogeneity in the CSOHG.

Secondary

MeasureTime frameDescription
the imaging phenotype of tumor heterogeneity with a multi-scale radiomic approach by obtaining the image mirror tumor at the in vivo scaleone shoot at the surgeryCorrelation between radiomic maps and pathogenic maps of heterogeneity,
tumor heterogeneity based on phenotypic imaging supported by AI reflects and can predict sub-histologyunderlying by tumor stroma proportion and tumor density infiltrating lymphocytes and genomics through HRDone shoot at the surgeryCorrelation between radiomic algorithms and i/underlying histology and ii/ genomics
the heterogeneity of the tumor biology of CSOHG through non-invasive habitat imaging combined with an integrated Multi-O-Mics approach.one shoot at the surgeryCorrelation between radiomic maps and tumor biology (CYTOF, proteomics and transcriptomics),
To Correlate MRI results with hematological molecular biology results.one shoot at the surgeryCorrelation between radiomic algorithms for tumor detection and cDNA determination.

Countries

France

Contacts

Primary ContactMOUSSION Aurore
aurore.moussion@icm.unicancer.fr0467613102
Backup ContactTexier Emmanuelle
emmanuelle.texier@icm.unicancer.fr0467613102

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026