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Clinical Trials in China / NCT06126393
Starting soon Observational

MRI Radiomics Combined With Pathomics on the Prediction of Molecular Classification and Prognosis of Endometrial Cancer

NCT06126393 · tracked via the Priya Life Science China tracker
Sponsor
Fujian Cancer Hospital
Phase
Observational
Started
2024-01-01
Last updated
2023-11-15

Condition(s) studied

Endometrial Neoplasms

Investigational drug(s) / intervention(s)

next generation sequencing AND Immunohistochemical examination

next generation sequencing AND Immunohistochemical examination: First, the mismatch repair (MMR) proteins were detected by immunohistochemistry, and the deletion of one or more proteins was classified as d-MMR subtype; Then the POLE gene mutation detection was performed, and the mutation Changes were classified as POLE mutation; Finally, p53 was detected by immunohistochemistry, and p53 mutant (p53 abn) and p53 wild-type (p53wt) were distinguished.

Study summary

Molecular typing provides accurate information for the diagnosis, treatment and prognosis prediction of endometrial cancer, which has important clinical significance. However, due to its high cost and complicated process, it is difficult to be widely used in clinical practice. Based on the artificial intelligence method, this study fused the characteristics of MRI radiomics and pathomics, combined with the clinical pathological information, built a model to predict the molecular typing and prognosis, analyzed the biological characteristics of endometrial cancer from the multi-scale level, guided the personalized and precise diagnosis and treatment, in order to improve the prognosis of patients.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * •Pathologically confirmed as endometrial malignant tumor with complete pathological H&E stained sections; * Age ≥ 18 years and ≤ 80 years; * No other malignant cancers was found; * The complete immunohistochemical and second-generation sequencing results can be used for the molecular typing of ProMisE; * Magnetic resonance examination was performed within 2 weeks before treatment, and there was at least one measurable lesion according to RECIST 1.1 Criteria. Exclusion Criteria: * • The image quality is poor or the tumor is too small due to serious graphic artifact and degeneration, and the ROI cannot be accurately delineated; * Patients who received any antitumor therapy before surgery; * Diagnostic endometrial biopsy before MRI

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital Fuzhou Fujian

More Fujian Cancer Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06126393 on ClinicalTrials.gov ↗ ← All trials in China