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Study on clinical application of personalized renal sparing technique and postoperative precision therapy for renal carcinoma

Study on clinical application of personalized renal sparing technique and postoperative precision therapy for renal carcinoma

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035890
Enrollment
Unknown
Registered
2020-08-19
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-08-24

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

Conditions

Renal Cell Carcinoma

Interventions

A:Standard non - blocking technique
A:No blocking technique for reserved stitches
A:Preoperative DSA superselective embolization has no blocking technique
A:"2+1" suture technique
C:The molecular expression levels of Mir-497-5P, EIF3D, Gankyrin and RASSF10 were detected in postoperative tumor tissues
D:The biopsy tissues were tested by gene in situ hybridization or single cell transcriptomic sequencing to predict sensitive targeted drugs. The individual renal carcinoma organ model was used to scre
E:therapy according to guide or experience

Sponsors

Department of Urology, The Third Affiliated Hospital of Naval Medical University, PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. To establish a personalized kidney-preserving surgery strategy for early localized renal carcinoma:CTA, MRI imaging examination; renal carcinoma of T1 stage assessed by imaging. Single lesion of unilateral kidney; Ability to sign informed consent; 2. Establish a risk prediction model for postoperative recurrence, metastasis and prognosis of renal carcinoma; The postoperative pathology was renal clear cell carcinoma; There was no other malignant tumor except renal carcinoma; Ability to sign informed consent; 3. Selection of personalized targeted therapies based on gene in situ hybridization, single-cell transcriptomic sequencing and other gene detection technologies:Receive molecular targeted therapy; Biopsy of metastatic or primary lesions was performed; No bone marrow, kidney, liver, heart and other functional impairment before treatment; No prior medical treatment against tumor; Postoperative histology confirmed renal clear cell carcinoma; Ability to sign informed consent.

Exclusion criteria

Exclusion criteria: 1. To establish a personalized kidney-preserving surgery strategy for early localized renal carcinoma;Multiple or bilateral renal tumor lesions; Previous history of renal surgery; Serious cardiovascular and cerebrovascular diseases; Failure of liver, kidney and respiratory function; 2. Establish a risk prediction model for postoperative recurrence, metastasis and prognosis of renal carcinoma; Non-renal clear cell carcinoma; Accompanied by other malignant tumors; Serious cardiovascular and cerebrovascular diseases; Failure of liver, kidney and respiratory function; 3. Selection of personalized targeted therapies based on gene in situ hybridization, single-cell transcriptomic sequencing and other gene detection technologies:Non-renal clear cell carcinoma; Serious cardiovascular and cerebrovascular diseases; Failure of liver, kidney and respiratory function; Patients with previous anti-tumor failures.

Design outcomes

Primary

MeasureTime frame
Intraoperative parameters;Postoperative hospitalization parameters;Postoperative follow-up parameters;PFS and OS time;Follow-up parameters after targeted therapy;

Secondary

MeasureTime frame
Major pathology response rate after targeted therapy;Patient satisfaction score;the changes of imaging;biomarkers;the comparison of efficacy of groups;

Countries

China

Contacts

Public ContactCui Xin-gang

Department of Urology, The Third Affiliated Hospital of Naval Medical University, PLA

cuixingang@smu.edu.cn+86 021 81887661

Outcome results

None listed

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