Study the efficacy and toxicity of SABR treatment for oligometastatic/oligoprogressive renal cell carcinoma; investigate the effectiveness and safety of SABR combined with targeted immunotherapy; conduct stratified analysis to identify the optimal beneficiary population; establish a biobank to screen for biomarkers; and use radiomics analysis to identify characteristics of sensitive populations.
This study is a non-randomized, prospective, registry-based trial that aims to enroll 60 patients with renal cancer who will be diagnosed and treated at our hospital between May 2024 and May 2026. Without altering the patients' systemic treatment plans, those who meet the inclusion criteria after MDT discussion will receive SBRT (Stereotactic Body Radiation Therapy) for all lesions/all metastatic lesions in addition to the guideline-recommended medications. The radiotherapy plan is based on the SABR-COMET protocol and Timmerman's constraints. Patient data will be collected, including general clinical information, toxicity assessments during treatment and in the acute phase, detailed imaging data, regular assessments of pain and quality of life, and evaluations of late radiation therapy responses.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
60
Without altering the patients' systemic treatment plans, patients who meet the inclusion criteria after MDT discussion will receive SBRT radiotherapy for all lesions/all metastatic lesions based on the guideline-recommended medications. The radiotherapy plan is based on the SABR-COMET protocol and Timmerman's constraints.
Progression-Free Survival
K-M survival curves
Time frame: Through study completion, an average of 2 year
2 Years Progression-Free Surial
K-M survival curves
Time frame: For all the patients, the time from the index of treatment to 2 years
2 Years Overall Survival
K-M survival curves
Time frame: For all the patients, the time from the index of treatment to 2 years
Life Quality Score
TESS score, scores range from 0 to 60, with higher values indicating better quality of life.
Time frame: Through study completion, an average of 2 year,at each follow-up visit,once a month.
Pain Score
VRS grading system, a five-point scale is used, with higher scores indicating more severe perceived pain.
Time frame: Through study completion, an average of 2 year,at each follow-up visit,once a month.
Acute Toxicity
Adopt CTCAE5.0 standard, a six-point scale is used, 0 to 5 scale, with higher scores indicating more severe adverse reaction.
Time frame: Through study completion, an average of 2 year,at each follow-up visit,once a month.
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