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Drug Sensitivity Profiling of Ascites-Derived Tumor Cells for Individualized Treatment in Epithelial Ovarian Cancer: A Prospective Controlled Study

Drug Sensitivity Profiling of Ascites-Derived Tumor Cells for Individualized Treatment in Epithelial Ovarian Cancer: A Prospective Controlled Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099821
Enrollment
Unknown
Registered
2025-03-28
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

Epithelial Ovarian Cancer

Interventions

Drug sensitivity group:Drug sensitivity results of tumor cells derived from ascites assisting chemotherapy regimen decision
Control group:none

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The participant voluntarily agrees to join the study, signs the informed consent form, has good compliance, and is willing to cooperate with follow-up. 2. Pathologically confirmed diagnosis of epithelial ovarian cancer. 3. Clinical or surgical pathological staging of stage III-IV. 4. Patients who experienced recurrence within one year after cessation of chemotherapy. 5. Sufficient ascites available for collection. 6. Patients not suitable for secondary cytoreductive surgery. 7. An expected survival time of at least 3 months.

Exclusion criteria

Exclusion criteria: 1. Patients with insufficient ascites for collection. 2. Patients who have undergone successful secondary cytoreductive surgery with no residual tumor. 3. Patients with other concurrent malignancies. 4. Patients unable to complete standardized clinical diagnosis and treatment. 5. Patients with incomplete clinical data or who cannot be followed up.

Design outcomes

Secondary

MeasureTime frame
Overall survival;Quality of life patients between two groups;Adverse Effect;

Primary

MeasureTime frame
tumor markers;progression-free survival;Circulatin Tumor Cell;objective response rate;

Countries

China

Contacts

Public ContactJiaxin Yang

Peking Union Medical College Hospital

yangjiaxin@pumch.cn+86 13661160998

Outcome results

None listed

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