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A Prospective Registry Study of Stereotactic Ablative Radiotherapy (SABR) for Oligometastatic/Oligometastatic Renal Cell Carcinoma

A Prospective Registry Study of Stereotactic Ablative Radiotherapy (SABR) for Oligometastatic/Oligometastatic Renal Cell Carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092877
Enrollment
Unknown
Registered
2024-11-25
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Renal Cell Carcinoma

Interventions

Experimental group:Stereotactic Body Radiation Therapy

Sponsors

Cancer Hospital Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. For patients with newly diagnosed M1 or moderately advanced renal cancer with moderate progression on systemic therapy, there is no restriction on the location and number of metastases, but all metastases are required to be safely given a curative radiotherapy dose after radiotherapy evaluation (a/ß value is 3, EQD2>=70Gy) 2. Age>=18 years 3. ECOG 0-3 points 4. Renal malignant tumors confirmed by pathological or imaging examinations, but the subtype is not limited 5. Have evaluable lesions 6. Patients with spinal cord compression or brain metastatic edema that obviously require surgical decompression will be evaluated by the radiotherapy department after decompression, and if the above doses can be safely administered, they can also be enrolled 7. Tolerable to radiotherapy and standard systemic therapy (targeted or target-immune combination therapy) 8. Life expectancy> 6 months 9. Informed consent can be signed 10. There are follow-up conditions

Exclusion criteria

Exclusion criteria: 1. Patients with other comorbidities who are unable to use or tolerate target-immune drugs: allergy to target-free drugs, active bleeding, ulcers, intestinal perforation, intestinal obstruction, uncontrollable hypertension, grade III.-IV cardiac insufficiency (NYHA criteria), severe liver and kidney insufficiency (grade IV), etc 2. The patient has other comorbidities and cannot tolerate radiotherapy 3. Complete response to first-line drug therapy (i.e., there is no treatable target for SABR) 4. Previous history of radiotherapy at the same site 5. Pregnant or lactating women 6. Have other serious medical comorbidities that are unable to participate in the study

Design outcomes

Primary

MeasureTime frame
Progression-Free Survival;

Secondary

MeasureTime frame
Acute Toxicity;Pain;Life Quality Score;2 Years Overall Survival;2 Years Progression-Free Surial;2 Years Overall Survival;

Countries

China

Contacts

Public ContactXiongjun Ye

Cancer Hospital Chinese Academy of Medical Sciences

yexiongjun@cicams.ac.cn+86 139 1038 0916

Outcome results

None listed

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