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Prognostic prediction of high-grade serous ovarian carcinoma by multimodal magnetic resonance and radiomic analysis

Prognostic prediction of high-grade serous ovarian carcinoma by multimodal magnetic resonance and radiomic analysis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400095087
Enrollment
Unknown
Registered
2024-12-31
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

High-grade serous ovarian carcinoma, HGSOC

Interventions

Residual lesion group:None
No residual lesion group:None

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 2. Multimodal magnetic resonance examination before treatment; 3. NACT candidates (patients with high disease burden (Fagotti score >= 8 points based on laparoscopic diagnosis, peritoneal dissemination, > 2 intestinal resections, mesenteric retraction, extensive small bowel involvement, stage IVB, with the exception of liver, spleen, and isolated cardiorenal lymph node metastases); 4. Patients who have received more than one cycle of NACT prior to IDS; 5. Documented follow-up for at least 6 months after chemotherapy.

Exclusion criteria

Exclusion criteria: Patients with other primary malignancies, pregnant, treated with PDS, and prior history of other chemotherapy or radiotherapy. In addition, patients who lost follow-up during chemotherapy cycles or who had missing clinical and imaging data or poor image quality were also excluded

Design outcomes

Primary

MeasureTime frame
Residual tumor;

Secondary

MeasureTime frame
Progression-free survival;Overall survival;

Countries

China

Contacts

Public ContactXiao Zhibo

The First Affiliated Hospital of Chongqing Medical University

202530@cqmu.edu.cn+86 23 89011721

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026