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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06084195
Other study ID # PROICM 2023-02 MRO
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 19, 2023
Est. completion date October 2029

Study information

Verified date December 2023
Source Institut du Cancer de Montpellier - Val d'Aurelle
Contact MOUSSION Aurore
Phone 0467613102
Email aurore.moussion@icm.unicancer.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date October 2029
Est. primary completion date October 2026
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

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

Locations

Country Name City State
France NOUGARET Stephanie Montpellier

Sponsors (1)

Lead Sponsor Collaborator
Institut du Cancer de Montpellier - Val d'Aurelle

Country where clinical trial is conducted

France, 

References & Publications (35)

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McPherson A, Roth A, Laks E, Masud T, Bashashati A, Zhang AW, Ha G, Biele J, Yap D, Wan A, Prentice LM, Khattra J, Smith MA, Nielsen CB, Mullaly SC, Kalloger S, Karnezis A, Shumansky K, Siu C, Rosner J, Chan HL, Ho J, Melnyk N, Senz J, Yang W, Moore R, Mungall AJ, Marra MA, Bouchard-Cote A, Gilks CB, Huntsman DG, McAlpine JN, Aparicio S, Shah SP. Divergent modes of clonal spread and intraperitoneal mixing in high-grade serous ovarian cancer. Nat Genet. 2016 Jul;48(7):758-67. doi: 10.1038/ng.3573. Epub 2016 May 16. — View Citation

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* Note: There are 35 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary 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. The diagnostic performance of the radiomic and multiomic algorithm for the characterization of heterogeneity in the CSOHG. one shoot at the surgery
Secondary the imaging phenotype of tumor heterogeneity with a multi-scale radiomic approach by obtaining the image mirror tumor at the in vivo scale Correlation between radiomic maps and pathogenic maps of heterogeneity, one shoot at the surgery
Secondary 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 HRD Correlation between radiomic algorithms and i/underlying histology and ii/ genomics one shoot at the surgery
Secondary the heterogeneity of the tumor biology of CSOHG through non-invasive habitat imaging combined with an integrated Multi-O-Mics approach. Correlation between radiomic maps and tumor biology (CYTOF, proteomics and transcriptomics), one shoot at the surgery
Secondary To Correlate MRI results with hematological molecular biology results. Correlation between radiomic algorithms for tumor detection and cDNA determination. one shoot at the surgery
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