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Clinical trials on the safety and effectiveness of neoadjuvant stereotactic radiotherapy combined with surgical treatment for patients with renal cell carcinoma with inferior vena cava tumor thrombus

Clinical trials on the safety and effectiveness of neoadjuvant stereotactic radiotherapy combined with surgical treatment for patients with renal cell carcinoma with inferior vena cava tumor thrombus

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800015118
Enrollment
Unknown
Registered
2018-03-08
Start date
2018-04-01
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

renal cancer

Interventions

Case series:neoadjuvant stereotactic radiotherapy

Sponsors

Department of Urology, Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged = 18 years; 2. Radiographic evidence of renal cancer with inferior vena cava(IVC) tumor thrombus; 3. Tumor thrombus must be = Mayo Level II; 4. Patient eligible for stereotactic radiotherapy(SBRT) to the IVC tumor thrombus as decided by the treating radiation oncologist; 5. Patient eligible for IVC tumor thrombectomy as decided by the treating urologist; 6. Performance status ECOG 0-2; 7. Subjects must be able to undergo either a contrast enhanced MRI or CT; 8. Ability to understand and the willingness to sign a written informed consent.

Exclusion criteria

Exclusion criteria: 1. Subjects who have had radiotherapy to area of renal cancer or IVC tumor thrombus; 2. Subjects may have received targeted therapy, chemotherapy or any other investigational agents; 3. Subjects with a history of pulmonary embolism are excluded; 4. Subjects who are unable to tolerate SBRT or operation are excluded, such as severe cardiopulmonary insufficiency, severe arrhythmia, myocardial infarction, angina pectoris, severe coagulant disease, severe liver disease and so on; 5. Subjects who had eriously affecting the patient's judgement of disease are excluded, such as psychosis.

Design outcomes

Primary

MeasureTime frame
Mayo level of tumor thrombus;length of the corresponding anatomical mark of the tumor thrombus;Inferior vena cava wall invasion;Adverse reaction of SBRT in 4-6 weeks;Relapse-free survival;cancer-specific survival;overall survival;Perioperative complications;operation time;Intraoperative blood loss;

Secondary

MeasureTime frame
The longest diameter of the tumor;node status;

Countries

China

Contacts

Public ContactMa Lulin

Peking University Third Hospital

malulin@medmail.com.cn+86 13701010872

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 13, 2026