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A Study on the Consistency Verification between In Vitro Drug Sensitivity of Refractory and Recurrent Gynecological Tumors Based on Organoid Chips and AI Image Analysis and Real-World Clinical Efficacy

A Study on the Consistency Verification between In Vitro Drug Sensitivity of Refractory and Recurrent Gynecological Tumors Based on Organoid Chips and AI Image Analysis and Real-World Clinical Efficacy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500105748
Enrollment
Unknown
Registered
2025-07-10
Start date
2025-07-10
Completion date
Unknown
Last updated
2025-07-14

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

Conditions

Ovarian malignant tumors (before and after neoadjuvant chemotherapy for advanced stage, platinum-sensitive recurrence, platinum-resistant recurrence) 2. Cervical cancer (primary treatment for advanced stage, recurrent metastasis) 3. Endometrial cancer (primary treatment for advanced stage, recurrent metastasis) 4. Uterine sarcoma (initial treatment, recurrent metastasis)

Interventions

Refractory and Recurrent Endometrial Cancer Group:None
Refractory and Recurrent Ovarian Malignant Tumor Group:None
Refractory and Recurrent Uterine Sarcoma Group:None
Refractory and Recurrent Cervical Cancer Group:None

Sponsors

HenanCancerHospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.The subjects voluntarily joined this clinical study and signed an informed consent form, were able to cooperate with follow-up, and had good compliance; 2.Women aged 18-75 (including 18 and 75 years old, calculated on the day of signing informed consent); 3.Ovarian malignant tumors (before and after neoadjuvant chemotherapy for advanced stage, platinum-sensitive recurrence, platinum-resistant recurrence) 2. Cervical cancer (primary treatment for advanced stage, recurrent metastasis) 3. Endometrial cancer (primary treatment for advanced stage, recurrent metastasis) 4. Uterine sarcoma (initial treatment, recurrent metastasis); 4.ECOG rating: 0-1 points; 5.Expected survival period >= 3 months;

Exclusion criteria

Exclusion criteria: 1.Previous (within 5 years) or concurrent untreated malignant tumors, excluding cured skin basal cell carcinoma and carcinoma in situ; 2.Known cases of brain metastasis or meningeal metastasis (excluding those with stable disease control for >= 4 weeks after radiotherapy or surgery for brain metastasis);

Design outcomes

Primary

MeasureTime frame
Complete Response (CR);Partial Response (PR);Progressive Disease (PD);Stable Disease (SD),;Not Evaluable (NE);

Secondary

MeasureTime frame
Individual organoid in vitro drug sensitivity results (images), tumor inhibition rate.;

Countries

China

Contacts

Public ContactWEIBING

HenanCancerHospital

1140881981@qq.com+86 371 6558 7578

Outcome results

None listed

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