RecruitingNCT07305727

A Radiomic MRI Predictive Model for Response to Concomitant Chemoradiotherapy in Locally Advanced Cervical Cancer

Developing a Radiomic MRI Model Predictive of Response to Concomitant Chemoradiotherapy in Locally Advanced Cervical Cancer. A Prognostic, Retrospective, Open-label, Multicenter, Descriptive and Analytical Clinical Cohort Study


Sponsor

Centre Hospitalier Universitaire de Nīmes

Enrollment

120 participants

Start Date

Jan 1, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

Cervical cancer is the fourth most common cancer in women worldwide, with approximately 604,000 new cases in 2020.Treatment for locally advanced cervical cancer is based on a combination of radiotherapy and chemotherapy. The response to concomitant chemoradiotherapy vary from one woman to another. Predicting the response to these treatments would allow early consideration of alternative therapies for patients identified as less responsive to standard treatments. A 5-year recurrence-free survival is approximately 79% for stages IB and IIA and 59% for stages III and IVA, with approximately 36% of local failures despite chemoradiotherapy. In a few studies,the radiomic MRI approach in locally advanced cervical cancers has shown to be prognostic for locoregional recurrence or survival but these models still need to be explored and validated.The EPICOL cohort, a clinical-biological cohort of 136 patients treated with chemoradiotherapy for locally advanced cervical cancer at the Montpellier Cancer Institute or Nîmes University Hospital, will be used to develop a predictive model of response to chemoradiotherapy based on radiomic data from pelvic MRIs before and after treatment.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study uses advanced MRI image analysis (called radiomics) to build a model that can predict how well patients with locally advanced cervical cancer will respond to standard chemoradiotherapy — radiation combined with chemotherapy — before treatment begins. **You may be eligible if...** - You have been treated with chemoradiotherapy alone (no surgery) for locally advanced cervical cancer (stages Ib–IVb) - At least 2 years have passed since your treatment - A tissue sample (biopsy) from before your treatment is still available - You are affiliated with or covered by a French health insurance plan **You may NOT be eligible if...** - You did not receive chemoradiotherapy as your main treatment - Less than 2 years of follow-up data are available - Your pre-treatment biopsy is unavailable Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

Nimes University Hospital

Nîmes, Gard, France

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NCT07305727


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