Actively Recruiting

Age: 18Years +
All Genders
NCT06120374

Adjuvant Radioimmunotherapy Compared With Adjuvant Chemotherapy for UTUC

Led by Peking University First Hospital · Updated on 2025-12-30

178

Participants Needed

3

Research Sites

387 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is an ambispective cohort observational study to analyze the efficacy of adjuvant radioimmunotherapy (radiotherapy and immunotherapy) compared with adjuvant chemotherapy in patients with the upper urinary tract urothelial carcinoma with high-risk factors (postoperative pathology suggestive of pT2 and above, N+, G3/high-grade and multiple tumors, positive cut margins). A subgroup analysis was performed to obtain the population of patients who might benefit from different treatment approaches. Patients with high risk factors for postoperative recurrence or metastasis will be treated with relevant adjuvant therapy, which in turn will benefit patients.

CONDITIONS

Official Title

Adjuvant Radioimmunotherapy Compared With Adjuvant Chemotherapy for UTUC

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of upper urinary tract urothelial carcinoma (UTUC)
  • High-risk UTUC including stage pT2 or higher, lymph node positive, tumor grade 3, multiple tumors, or positive surgical margins
  • 18 years of age or older
Not Eligible

You will not qualify if you...

  • Presence of distant metastases at surgery or incomplete tumor removal (non-R0 resection)
  • Prior pelvic or abdominal radiotherapy, history of inflammatory bowel disease, or previous systemic chemotherapy
  • Pregnant or breastfeeding women, or women of childbearing potential not using reliable contraception
  • History of other malignant tumors except certain skin cancers and cervical cancer cured over 5 years ago
  • Weight loss over 10% in the last 6 months
  • Bleeding disorders or active infections
  • Poor health condition unable to tolerate treatment
  • Unable to provide informed consent due to psychological, family, social, or other reasons

AI-Screening

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Trial Site Locations

Total: 3 locations

1

Departmeng of Urology, Peking University First Hospital

Beijing, China

Actively Recruiting

2

Department of Medical Oncology, Peking University First Hospital

Beijing, China

Actively Recruiting

3

Department of Radiotherapy Oncology, Peking University First Hospital

Beijing, China

Actively Recruiting

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Research Team

X

Xuesong Li, M.D.

CONTACT

C

Chunru Xu, 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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Adjuvant Radioimmunotherapy Compared With Adjuvant Chemotherapy for UTUC | DecenTrialz