Actively Recruiting

Age: 18Years +
All Genders
NCT05595408

Circulating and Urine Tumor DNA Dynamics Predict Minimal Residual Disease and Recurrence Risk in Locally Advanced Upper Tract Urothelial Carcinoma

Led by RenJi Hospital · Updated on 2025-12-09

84

Participants Needed

1

Research Sites

256 weeks

Total Duration

On this page

Sponsors

R

RenJi Hospital

Lead Sponsor

W

West China Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

In our study, the ultra-deep sequencing of circulating tumor DNA (ctDNA) and urine tumor DNA (utDNA) were performed to assess whether ctDNA and utDNA can be used as predictive biomarkers for the detection of minimal residual disease (MRD) and early diagnosis of UTUC recurrence, and explored the role of ctDNA and utDNA detection of MRD in the prediction of adjuvant therapy efficacy and prognostic evaluation.

CONDITIONS

Official Title

Circulating and Urine Tumor DNA Dynamics Predict Minimal Residual Disease and Recurrence Risk in Locally Advanced Upper Tract Urothelial Carcinoma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Pathologically confirmed upper tract urothelial carcinoma at stage T2-4 or with lymph node involvement (N+) and no distant metastasis (M0)
  • Male or female aged 18 years or older willing to sign informed consent
  • ECOG performance status between 0 and 2
  • Underwent radical nephroureterectomy for upper tract urothelial carcinoma
  • No history of multiple primary carcinomas
  • Received adjuvant chemotherapy or immunotherapy within 12 weeks after surgery
  • At least two postoperative liquid biopsy assessments (T1 and T2)
Not Eligible

You will not qualify if you...

  • Prior history of bladder cancer or concurrent bladder cancer
  • Pregnant or breastfeeding women, or fertile patients not using contraception
  • Severe infection
  • Serious heart disease
  • Uncontrolled neurological or mental disorders
  • Severe diabetes mellitus
  • Severe autoimmune diseases
  • Exposure to neoadjuvant therapy
  • No bilateral upper tract urothelial carcinoma
  • Surveillance period less than one month
  • Fewer than two postoperative minimal residual disease surveillance assessments

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Renji Hospital

Shanghai, Shanghai Municipality, China, 200127

Actively Recruiting

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Research Team

J

jiwei huang, M.D

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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