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A Prospective Cohort Study Comparing Surgical Outcomes and Prognostic Factors in Patients with Clinical T3a Renal Cell Carcinoma

A Prospective Cohort Study Comparing Surgical Outcomes and Prognostic Factors in Patients with Clinical T3a Renal Cell Carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129175
Enrollment
Unknown
Registered
2026-07-31
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

renal cell carcinoma

Interventions

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Patients with clinical T3a renal cell carcinoma who are scheduled to undergo surgical treatment at our center; 2.Patients aged 18–75 years; 3.Imaging findings consistent with renal cell carcinoma, with suspected T3a-related features such as perinephric fat invasion, renal sinus fat invasion, invasion of the renal vein or its branches, or collecting system invasion; 4.No evidence of distant metastasis on preoperative evaluation; 5.Patients who voluntarily participate in the study, provide written informed consent, and are willing to complete the scheduled follow-up.

Exclusion criteria

Exclusion criteria: 1.Preoperative imaging indicating tumor extension into the inferior vena cava, beyond the renal fascia, or into adjacent organs, suggesting clinical stage T3b, T3c, or T4 disease; 2.Presence of distant metastasis or definite unresectable lymph node metastasis; 3.A history of surgery on the ipsilateral kidney; suspected severe adhesion between the ipsilateral kidney and surrounding tissues; or special conditions such as a solitary kidney, bilateral renal tumors, or severe chronic renal insufficiency; 4.Presence of another concurrent malignant tumor; 5.Underlying medical conditions that preclude tolerance of surgery; 6.Inability to understand the study, provide written informed consent, or complete the required follow-up.

Design outcomes

Primary

MeasureTime frame
Estimated glomerular filtration rate (eGFR);Progression-free survival (PFS);Cancer-specific survival (CSS);Overall survival (OS);

Secondary

MeasureTime frame
Operative time;Intraoperative blood loss;Perioperative blood transfusion;Conversion to open surgery or intraoperative change in surgical approach;length of stay;Duration of postoperative drainage;Postoperative complications and Clavien–Dindo classification;Pathological invasion pattern;

Countries

China

Contacts

Public ContactLiu Kan

Chinese PLA General Hospital

liukan_plagh@163.com+86 10 6693 6394

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026