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Study identifier: NCT06583070 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

SABR Combined With Targeted Therapy and Anti-PD-1 for Recurrent or Metastatic Renal Cancer

Condition: Radiation Therapy · Metastatic Renal Cancer · Recurrent Renal Cell Cancer  ·  Sponsor: Peking University First Hospital

PhaseN/A
Planned participants300
Who can joinMale, 18 Years to 85 Years
Healthy volunteersNo

About this study

Renal cancer ranks seventh in incidence among men and sixth among women in the Beijing area, with Peking University First Hospital treating over 1,000 kidney cancer patients annually. Once recurrence or metastasis occurs, the prognosis is poor, with median progression times of 1-2 years after first-line systemic therapy (targeted therapy combined with immunotherapy). Enhancing local control of lesions is key to improving overall survival. Combining local radiotherapy with systemic treatment may be one approach to address this issue. Currently, Stereotactic Ablative Radiotherapy (SABR) enables precise tumor ablation and can activate the body's immune response. Studies show that the one-year local control rate after SABR exceeds 90%. Preliminary research by the applicant has shown that the combination of drug therapy and SABR for recurrent metastatic renal cancer can extend progression-free survival beyond two years, with earlier intervention leading to more significant survival improvements. This study aims to evaluate the efficacy and safety of combining SABR with targeted and immunotherapy for recurrent metastatic renal cancer through a multicenter, bidirectional cohort design, exploring new therapeutic strategies.

This description comes directly from the study's public registry record.

Talk to the study team

Mingwei Ma, M.D.  ·  +86-15810160120  ·  dr.mingweima@stu.pku.edu.cn

Always discuss trial participation with your own doctor first.

Locations (2)

Peking University First HospitalBeijing, Beijing Municipality, ChinaRecruiting
Peking University Third HospitalBeijing, Beijing Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06583070