Skip to content

MRI-based Signatures for Survival Prediction in Cervical Cancer With Radiotherapy

A Prognostic Model Based on MRI for Cervical Cancer Patients Treated With Radiotherapy

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06197126
Enrollment
200
Registered
2024-01-09
Start date
2024-01-01
Completion date
2028-12-31
Last updated
2024-01-09

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

Conditions

Cervical Cancer, MRI, Prognostic Model, Radiotherapy

Brief summary

This study aims to validate the value of tumor involvement features based on MRI in cervical cancer, facilitate the development of a more appropriate model for risk stratification, and help patients with varying risk profiles make appropriate decisions in treatment selection and follow-up plans.

Detailed description

Even with the development of advanced technology, the prognosis for CC patients who received radiotherapy is still an intractable problem. Almost 40% suffered disease recurrence among locally advanced patients after radiotherapy and the reported 5-year overall survival is 50-70%. The present FIGO staging is controversial in pre-treatment assessment, which is mainly based on physical examination. An ambiguous diagnosis leads to different treatment strategies and follow-up plans, which is associated with prognosis non-improvement. Incorporation of the tumor involvement features based on the MRI into pre-treatment assessment could standardize and improve the consistency and repeatability of diagnosis.

Interventions

RADIATIONTreatment mainly composed of external pelvic beam radiotherapy (EBRT) followed by individualized high-dose-rate intracavitary brachytherapy (HDR-ICBT) .

The chemotherapy regimens included cisplatin (40 mg/m2) or nedaplatin (80 mg/m2) monotherapy or combined with paclitaxel (135 mg/m2) every three weeks during radiotherapy.

Sponsors

Fujian Cancer Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* (1) pathologically confirmed CC, (2) initially treated in our center

Exclusion criteria

* (1) lack of pre-treatment MRI, (2) prior anti-tumor treatment, (3) pelvic surgery history, (4) incomplete therapy, (5) loss of follow-up

Design outcomes

Primary

MeasureTime frameDescription
overall survival1-36 monthsthe interval from diagnostic day to death or the last follow-up

Secondary

MeasureTime frameDescription
progression-free survival1-36 monthsthe interval from diagnostic day to death, the last follow-up, or the onset of regional recurrence or distant metastasis

Countries

China

Contacts

Primary ContactYang Sun
sunyang@fjzlhospital.com+8615959028989

Outcome results

None listed

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