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

Recruiting now

Conditions studied: Uterine Cervical Neoplasms, Cervical Cancer by FIGO Stage 2018

In brief

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.

Key facts

Study ID

NCT07305727

Run by

Centre Hospitalier Universitaire de Nīmes

People needed

120

Starts

2026-01-01

Expected to finish

2026-12-31

Last updated by the study team

2026-01-07

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Patients treated with exclusive radio-chemotherapy for locally advanced cervical cancer (stage Ib-IVb according to the FIGO classification).
• Patients with a minimum of 2 years of post-treatment follow-up.
• Patients for whom the initial biopsy specimen (prior to treatment) is available.
• Patients who have not expressed their opposition to participating in the study.
• Patients who are affiliated with or beneficiaries of a health insurance plan.

You may not qualify if…

• Patients under judicial protection, guardianship, or curatorship

Where it is running

• Nimes University Hospital — Nîmes, Gard, France (enrolling)

Full record on ClinicalTrials.gov

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