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NCT Number: NCT06467097

Systemic Treatment Alone Versus Systemic Treatment Plus Radiotherapy in Oligometastatic Renal Cell Carcinoma

To evaluate whether incorporating locoregional radiotherapy in the treatment of oligometastatic renal cell carcinoma, including inductive oligometastases, along with standard systemic therapy, contributes to improved progression-free survival rates for patients.

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Key information

Age range

20 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

About this study

Various institutions are attempting to use locoregional radiotherapy in the treatment of oligometastatic renal cell carcinoma, accompanied by a few metastases. Research findings have indicated that high-dose locoregional radiotherapy can suppress disease progression, potentially prolonging the interval for additional systemic therapy; however, whether the addition of locoregional radiotherapy in cases of renal cell carcinoma with oligometastases demonstrates superior oncologic outcome compared to standard systemic therapy alone has yet to be established. Therefore, a randomized phase III study is being conducted to evaluate whether incorporating locoregional radiotherapy in the treatment of oligometastatic renal cell carcinoma, including inductive oligometastases, along with standard systemic therapy, contributes to improved progression-free survival rates for patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with metastatic renal cell carcinoma classified within the ESTRO/EORTC classification system as having ≤ 5 metastases, ≤ 3 metastatic organs, and meeting criteria for new, recurrent, or induced metastases.
  • Patients aged 20 to 80 years.
  • Patients with individual metastases ≤ 5 cm in longest diameter.
  • Patients with primary tumors surgically removed or scheduled for surgery.
  • Patients histologically diagnosed with clear cell carcinoma.
  • Patients with ECOG performance status 0-1.
  • Patients with normal major organ function and bone marrow function meeting specific criteria: WBC ≥ 2,000/μL, neutrophils ≥ 1,000/μL, platelets ≥ 50,000/μL.
  • Patients who understand the contents of the informed consent form, voluntarily consent to participate in the study, and sign the informed consent form.
  • Patients who agree to use contraception from the time of signing the consent form until 1 year after the last standard systemic therapy.
  • Breastfeeding women who agree to stop breastfeeding for at least 5 months after the last standard systemic therapy.
  • Patients with visible tumors outside the scope of tumor removal surgery (surgical therapy) for metastatic lesions.

Exclusion criteria

  • Patients with total bilirubin > 3.6 mg/dL.
  • Patients with AST >160 U/L, ALT > 165 U/L.
  • Patients unable to maintain position for partial nephrectomy radiotherapy.
  • Patients with a history of radiotherapy to metastatic renal cell carcinoma or surrounding areas.
  • Patients with confirmed brain, peritoneal, or pleural metastases.
  • Patients diagnosed with another solid tumor and treated within 2 years or with residual lesions.
  • Patients who do not consent to participate in the study.
  • Pregnant patients.

Treatment and study plan

SBRT(Stereotatic Body Radiation Therapy)

Radiation

Patients will receive treatment for one to two weeks, one to five times per region.

Primary outcomes

  1. 1-year progression-free survival rate

    Time frame: One year after completion of enrollment

    Compare free survival between the standard systemic therapy alone group and systemic therapy combined with radiotherapy group

Secondary outcomes

  1. Local control rate for radiation therapy site at one year

    Time frame: One year after radiation completion of each participant

    Compare Local control rate between the standard systemic therapy alone group and systemic therapy combined with radiotherapy group

  2. Grade 3 acute adverse event

    Time frame: three to six months after study treatment

    Compare acute adverse events according to CTCAE V5.0 between the standard systemic therapy alone group and systemic therapy combined with radiotherapy group

  3. Grade 3 chronic adverse event

    Time frame: one year to three years after radiation completion

    Compare chronic adverse events according to CTCAE V5.0 between the standard systemic therapy alone group and systemic therapy combined with radiotherapy group

  4. Overall survival rate

    Time frame: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 36 months

    Compare Overall survival rate between the standard systemic therapy alone group and systemic therapy combined with radiotherapy group

Study contacts

Contact information is provided by the study sponsor or research team.

Won Park, M.D., Ph.D.

CONTACT

[email protected]

+82-2-3410-2616

Sponsors and collaborators

Lead sponsor

Samsung Medical Center

Other

Registry information

Official study title

A Phase Ⅲ Randomized Study Systemic Treatment Alone Versus Systemic Treatment Plus Stereotactic Abative Body Radiotherapy for Patients With Oligometastatic Renal Cell Carcinoma: SABLOR Study

Acronym: SABLOR

Important dates

Study start
2024
Primary completion
2031
Study completion
2031
First posted
Jun 20, 2024
Registry last updated
Jun 20, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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