Prognosis of Patients With Upper Tract Urothelial Carcinoma Receiving Kidney-sparing Therapy

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorRenJi Hospital

About this trial

Upper tract urothelial carcinoma (UTUC) is a rare malignant disease which accounts for 5-10% of urothelial carcinoma in the western world and 9%-30% in China. About two thirds of patients have muscle invasive disease at diagnosis. Those patients usually have poor prognosis. The 5 year cancer specific survival is \<50% for pT2/T3 and \<10% for pT4. Radical nephroureterectomy is the standardized treatment for non-metastatic high risk UTUC. However, about half patients may suffer from impaired renal function after nephroureterectomy. On the other hand, kidney sparing surgery can avoid renal function impairment, but the therapy is only recommended for few patients with low-risk disease. The treatment for urothelial carcinoma has changed rapidly in the past few years. Immune checkpoint inhibitors and novel agents such as ADCs have shown promising therapeutic effect and were approved for patients with metastatic UTUC. Meanwhile, a recent study shows that patients with high-risk disease can also receive kidney sparing surgery without compromising cancer specific survival and overall survival. This prospective, observational study aims to evaluate the prognosis of contemporary kidney sparing surgery in patients with UTUC with or without perioperative therapy in the real world.

Eligibility criteria

Qualifiers

Histopathological confirmed upper tract urothelial carcinoma;

Refused radical nephroureterectomy, or eligible for the indications of kidney-sparing surgery;

Participants must be willing to attend the follow-up visits;

Sign informed consent.

Disqualifiers

Unable to undergo kidney-sparing surgery;

Life expectancy < 6 months;

Previous anti-tumor therapy against UTUC, including systemic chemotherapy, surgery, radiotherapy, or immunotherapy identifying by investigators.

Trial design

Treatments tested in this trial

  • Observational

Treatment groups

106 Participants
are divided into 1 treatment group

Sponsors and collaborators

RenJi Hospital

Lead sponsor

Shanghai Zhongshan Hospital

Collaborator

Tianjin Medical University Second Hospital

Collaborator

Xiangya Hospital of Central South University

Collaborator

West China Hospital

Collaborator

Ruijin Hospital

Collaborator

First Affiliated Hospital Xi'an Jiaotong University

Collaborator

The First Affiliated Hospital of University of Science and Technology of China

Collaborator

The Second Hospital of Anhui Medical University

Collaborator

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Collaborator