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Clinical study of ctDNA dynamic monitoring and recurrence or metastasis of renal cell carcinoma after radical nephrectomy

Clinical study of ctDNA dynamic monitoring and recurrence or metastasis of renal cell carcinoma after radical nephrectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200055858
Enrollment
Unknown
Registered
2022-01-20
Start date
2022-01-20
Completion date
Unknown
Last updated
2023-07-02

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

Conditions

Renal cell carcinoma

Interventions

positive MRD:None
negative MRD:None

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients with high risk of recurrence who can receive radical nephrectomy; 2.Clinical stage: T2N0M0, T1/2N1M0,T3N0/1M0, T4N0/1M0; 3.Negative margin and there was no tumor residue; 4.The histopathological types of renal carcinoma are not limited: clear cell carcinoma and non-clear cell carcinoma; 5.Agree to provide archived tumor tissue samples or fresh tissue samples (tissue samples must be available) and blood samples at different time points; 6.ECOG PS Score of 0 to 2 points; 7.The expected survival is greater than 6 months; 8.Aged 18 to 80 years old; 9.Willing to sign informed consent; 10.Patients were able to follow up regularly, communicate well with the investigator, and complete the study according to study guidelines.

Exclusion criteria

Exclusion criteria: 1.Positive margin or residual lesions were found; 2.A patient with a prior history of other malignancies may not participate in the study unless he/she has been in complete remission for at least 5 years prior to enrollment and does not require other treatment or does not require other treatment during the study period; 3.Associated with serious medical conditions, including but not limited to uncontrolled diabetes, active gastrointestinal ulcers, active bleeding, etc; 4.Sample collection and preservation methods are not standardized; 5.Incomplete information about subjects; 6.Patients with insufficient communication, understanding, and cooperation, or poor compliance to ensure that follow-up is completed as required; 7.The investigator considers that subjects who are not suitable to participate in this clinical study for various other reasons will withdraw from the study or terminate the study treatment.

Design outcomes

Primary

MeasureTime frame
disease-free survival;

Secondary

MeasureTime frame
overall survival;

Countries

China

Contacts

Public ContactZhang Xu

Chinese PLA General Hospital

xzhang301@163.com+86 10 66936008

Outcome results

None listed

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