Radiation boost may extend life in advanced kidney cancer
NCT ID NCT06583070
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether adding a precise type of radiation (SABR) to standard drug therapy (targeted therapy plus immunotherapy) can help people with recurrent or metastatic kidney cancer live longer without their disease getting worse. About 300 participants will be enrolled, and researchers will compare outcomes between those who get radiation plus drugs versus drugs alone. The goal is to see if this combination improves local tumor control and overall survival.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 300 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2024
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with histologically confirmed renal cancer; diagnosed with recurrent or metastatic renal cancer via PET/CT or other whole-body imaging.
- Ages
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18 to 85 years
- Sex
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Male participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients with histologically confirmed renal cancer; diagnosed with recurrent or metastatic renal cancer via PET/CT or other whole-body imaging. * Evaluated by the radiation oncology and imaging departments as having at least one lesion amenable to radiation therapy. * Planning to undergo or currently receiving first-line or second-line targeted therapy combined with immunotherapy. * Voluntarily agrees to participate in the study and signs an informed consent form. * Male or female, aged ≥18 years (inclusive). * Expected survival of ≥12 weeks. * At least one measurable lesion as per the Response Evaluation Criteria in Solid Tumors (RECIST) 1.1. * European Cooperative Oncology Group (ECOG) performance status of 0 or 1. * Adequate cardiac, bone marrow, liver, and renal function. * Willing and able to comply with the study procedures and follow-up schedule. Exclusion Criteria: * Extensive, multiple metastases; * Presence of central nervous system metastases and/or carcinomatous meningitis. * Toxicity from previous treatments not yet recovered to grade 0-1 (excluding grade 2 alopecia); * Other severe, uncontrollable co-morbid conditions that could affect protocol compliance or confound interpretation of results, including active opportunistic or severe progressive infections, uncontrolled diabetes, uncontrolled hypertension, cardiovascular diseases (defined as New York Heart Association Class III or IV heart failure, second-degree or higher heart block, myocardial infarction within the last 12 months, unstable arrhythmias or angina, stroke within the last 6 months), or pulmonary diseases (interstitial pneumonia, obstructive pulmonary disease, and symptomatic bronchospasm history), deep vein thrombosis or pulmonary embolism within the last 6 months; * Diagnosed with other malignancies within 5 years prior to enrollment, except: * Localized low-risk prostate cancer (defined as stage ≤T2b, Gleason score ≤7, and PSA ≤20ng/mL at diagnosis, who have undergone curative treatment with no recurrence of prostate-specific antigen); * Malignancies treated with a curative intent that are considered cured, including but not limited to adequately treated thyroid cancer, cervical carcinoma in situ, basal or squamous cell skin cancer, or ductal carcinoma in situ of the breast treated with surgery; * Pregnant or breastfeeding women; * Positive HIV test result; * Active hepatitis B or C infection; * Active tuberculosis; * Any other conditions, metabolic abnormalities, physical examination or laboratory findings that in the investigator's judgment might indicate an unsuitability for the study drug, could interfere with the interpretation of study results, or place the patient at high risk if they participate in the study; * Estimated insufficient compliance with the clinical study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Peking University First Hospital
RECRUITINGBeijing, Beijing Municipality, 100034, China
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Peking University Third Hospital
RECRUITINGBeijing, Beijing Municipality, 100091, China
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Other studies related to the condition(s) this trial covers.
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