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NCT Number: NCT02141919

Stereotactic Ablative Body Radiation Therapy for Patients With Primary Renal Cancer

The goal of this phase II clinical trial is to evaluate the efficacy of the completely non-invasive treatment option of stereotactic radiation therapy for the treatment of biopsy proven and growing small renal tumors.

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This study is active but is not currently recruiting participants.

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Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

University of Texas Southwestern

Dallas, Texas, 75239, United States

About this study

Current treatment options for primary renal cancer include surgery or ablative techniques-all are invasive or minimally invasive options. The completely noninvasive treatment option of stereotactic radiation therapy (SABR), which has become standard of care in many cancer sites, has not been explored for primary renal cancer. With multiple technological advances, it is now feasible to safely treat a moving intra-abdominal tumor such as that in a kidney. This proposed clinical trial evaluates the efficacy of SABR in treating patients with early renal cancers. Growing renal masses will first be biopsied to confirm the diagnosis of renal cancer. Patients will then undergo treatment with SABR of 3-5 fractions completing within three weeks. Treatment response will be evaluated using sequential MRI scans and a second tumor biopsy one year after treatment. Monitoring of treatment toxicity and kidney function will also be performed.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 18 years.
  • Renal mass ≤ 5cm
  • The treating renal mass must be ≤ 5cm. Other renal masses (cysts etc.) of any size will not make the subject ineligible
  • Biopsy proven Renal neoplasm
  • All histology of renal cancers are included including oncocytoma
  • Growth of renal mass >2mm in radiographic scans must be demonstrated within a one year period.
  • Ability to understand and the willingness to sign a written informed consent.
  • Subject is able to undergo either an MRI or administration of contrast agent for CT
  • Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) for the duration of the study. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.
  • A female of child-bearing potential is any woman (regardless of sexual orientation, having undergone a tubal ligation, or remaining celibate by choice) who meets the following criteria:
  • Has not undergone a hysterectomy or bilateral oophorectomy; or
  • Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has had menses at any time in the preceding 12 consecutive months).

Exclusion criteria

  • Subject has received any treatment for the treating renal mass; such as RFA or cyroablation.
  • If other renal masses received RFA or cryoablation or surgery, then these patients are eligible.
  • Subjects received previous abdominal radiation
  • Evidence of Metastatic Disease, unless disease-free for ≥ 3 years prior to registration, (non-melanomatous skin cancer and in-situ cancers are okay).
  • Female subjects who are pregnant or planning to become pregnant during the course of SABR.

Treatment and study plan

Stereotactic Ablative Radiation Therapy

Radiation

Stereotactic Ablative Body Radiation Therapy (SABR): 3 fractions of 12Gy, or 4 fractions of 10Gy or 5 fractions of 8 Gy

Other names: SABR

Primary outcomes

  1. Eliminate its growth and tumor viability.

    Time frame: 2 years

    To evaluate if SABR to small renal tumors is able to eliminate its growth and viable tumor.

Secondary outcomes

  1. Adverse events

    Time frame: 2 years

    To describe the adverse events associated with the administration of SABR to renal tumors.

  2. growth rate of renal tumors

    Time frame: 2 years

    To measure the growth rate of renal tumors after SABR treatment.

  3. Renal function

    Time frame: 2 years

    To measure the changes in kidney function, creatinine levels, renal perfusion and GFR after SABR treatment

  4. Tumor Viability

    Time frame: one year

    To measure tumor viability pathologically one year after SABR treatment with biopsy.

  5. progression of disease

    Time frame: 2 years

    To assess radiographic changes to the renal tumor after SABR treatment including tumor viability, enhancement necrosis,T2 tumor cellularity with diffusion-weighted imaging. To assess local, regional and systemic progression of disease after SABR to SRM .To assess time to progression (TTP) of disease from the first SABR treatment.

    To assess progression free survival (PFS). PFS is defined as the length of time from start of treatment to the time of loco-regional disease progression or death from any cause.

    To assess overall survival (OS). OS is defined as the duration of time from start of treatment to the time of death from any cause.

    To assess tumor growth, local failure and indeterminate disease response (IDR).

Sponsors and collaborators

Lead sponsor

University of Texas Southwestern Medical Center

Other

Registry information

Official study title

A Phase II Trial of Stereotactic Ablative Body Radiation Therapy (SABR) for Patients With Primary Renal Cancer (RCC)

Important dates

Study start
2013
Primary completion
2026
Study completion
2026
First posted
May 20, 2014
Registry last updated
Dec 26, 2025

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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