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To construct a predictive model for the efficacy of immunotherapy for endometrial cancer based on peripheral blood parameters

To construct a predictive model for the efficacy of immunotherapy for endometrial cancer based on peripheral blood parameters

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096235
Enrollment
Unknown
Registered
2025-01-20
Start date
2025-01-20
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Endometrial Cancer

Interventions

Disease progression group:None

Sponsors

Jilin Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Endometrial cancer was diagnosed by clinicopathological examination. At least one lesion was evaluable according to RECIST1.1 criteria. Age >= 18 years old; 2.Patients completed at least 2 cycles of PD-1/PD-L1 monoclonal antibody treatment. The relevant clinical data and prognosis of the patients were complete. Informed consent was obtained from all patients before treatment.

Exclusion criteria

Exclusion criteria: 1.Combined with other malignant tumors; 2.Acute and chronic infectious diseases; 3.Patients with previous immune system diseases or severe immune adverse reactions during treatment; 4.Patients with heart, liver, kidney, lung and other body organ dysfunction; 5.Patients with cognitive dysfunction and mental disorders; 6.Patients were lost to follow-up.

Design outcomes

Primary

MeasureTime frame
Immunotherapy Efficacy;

Countries

China

Contacts

Public ContactJing Li

Jilin Cancer Hospital

lijinglixiang@126.com+86 431 80596230

Outcome results

None listed

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