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

Peking University

Status: Enrolling

Conditions: Radiation Therapy; Recurrent Renal Cell Cancer; Metastatic Renal Cancer

Treatments: Radiation: Radiation therapy; Drug: Targeted and immunotherapy

Study type: Observational

Funder types: Other

Identifiers

NCT06583070

COSTAR-001

Details and patient eligibility

About

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.

Enrollment: 300 estimated patients

Sex: Male

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

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.

Trial design

300 participants in 2 patient groups

RT group

Description:

In conjunction with targeted and immunotherapy, administer radiation therapy to achieve as complete coverage as possible of all identifiable primary and metastatic lesions.

Treatment:

Drug: Targeted and immunotherapy

Radiation: Radiation therapy

Control group

Description:

Targeted and immunotherapy

Treatment:

Drug: Targeted and immunotherapy