Skip to content

A Multi-center study for patient-derived tumor xenograft pharmacodynamic detection guided individualized treatment of advanced gynecological system tumor patients

A Multi-center study for patient-derived tumor xenograft pharmacodynamic detection guided individualized treatment of advanced gynecological system tumor patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800018422
Enrollment
Unknown
Registered
2018-09-17
Start date
2018-10-10
Completion date
Unknown
Last updated
2018-09-24

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

Conditions

Advanced gynecological system tumors

Interventions

Case series:Individualized chemotherapy

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Female, age 18 to 75 years old; 2. Pathological histological examination of advanced gynecologic tumors, requiring anticancer drug chemotherapy; 3. Can take surgical resection or biopsy to obtain fresh tumor tissue; 4. With objective tumors in accordance with RECIST 1.1, CT/MRI can be used to evaluate the efficacy; 5. The ECOG score is 0~2, and the expected survival period must be =3 months; 6. In the case of postoperative subjects, the previous anticancer drug treatment (chemotherapy and / or targeted therapy) failed to enter the group for = 4 weeks, and the adverse reactions have basically recovered; 7. Subjects volunteered to participate, signed informed consent, good compliance, active treatment and follow-up.

Exclusion criteria

Exclusion criteria: 1. Participate in other drug clinical studies at the same time; 2. Liver, kidney function and bone marrow hematopoietic function do not meet the requirements of chemotherapy; 3. Reluctant to use the anti-cancer drugs or regimens recommended by the investigator in combination with the results of this test for subsequent chemotherapy after the previous treatment failure; 4. Those with severe uncontrolled acute infections or major organ diseases; 5. Women who are pregnant or breastfeeding.

Design outcomes

Primary

MeasureTime frame
ORR;DCR;

Countries

China

Contacts

Public ContactMeng yuanguang

Chinese PLA General Hospital

rubyyangwen@sina.com+86 025-80864029

Outcome results

None listed

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