Interstitial Brachytherapy for the Treatment of Unresectable/Unablatable Kidney Cancer

NCT ID: NCT04473781

Last Updated: 2025-07-29

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 17 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-07-16
• Study Completion Date: 2027-06-30

Brief Summary

This phase I/II trial investigates the side effects of interstitial brachytherapy and to see how well it works in limiting the growth of large kidney cancer masses in patients with kidney cancer that have refused or are unable to undergo surgery or ablation (unresectable/unablatable). Brachytherapy, also known as internal radiation therapy, temporarily introduces a radiation source into or near the tumor to eradicate the tumor cells. Giving brachytherapy may potentially reduce the size of the kidney cancer mass that would otherwise not be amenable to surgical management and translate into lower risk of spread.

Detailed Description

PRIMARY OBJECTIVES:

I. To determine the safety and feasibility of renal interstitial radiation therapy (interstitial brachytherapy). (Safety Lead-In) II. To evaluate local control of renal interstitial brachytherapy. (Expansion Phase)

SECONDARY OBJECTIVES:

I. To evaluate treatment response of the primary tumor. II. To evaluate 12 month distant progression free survival. III. To evaluate the 12 month volumetric growth of the primary tumor mass. IV. To determine biomarkers predicting response and resistance to radiation treatment.

OUTLINE:

Patients undergo interstitial brachytherapy for 1-2 fractions in the absence of disease progression or unacceptable toxicity. Patients who undergo 2 fractions may receive both fractions in the same day or on 2 separate days over 2 weeks.

After completion of study treatment, patients are followed up every 3 months for at least 3 years.

Conditions

Stage I Renal Cell Cancer; Stage II Renal Cell Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment (interstitial brachytherapy)

Patients undergo interstitial brachytherapy for 1-2 fractions in the absence of disease progression or unacceptable toxicity. Patients who undergo 2 fractions may receive both fractions in the same day or on 2 separate days over 2 weeks.

Group Type: EXPERIMENTAL

Interstitial Radiation Therapy

Intervention Type: PROCEDURE

Undergo interstitial brachytherapy

Interventions

Interstitial Radiation Therapy

Undergo interstitial brachytherapy

Intervention Type: PROCEDURE

Other Intervention Names

BRACHYTHERAPY, INTERSTITIAL; Implant Radiation

Eligibility Criteria

Inclusion Criteria

• Elected to undergo interstitial brachytherapy as part of conventional treatment for renal cell carcinoma
• Biopsy proven renal cell carcinoma
• No definitive evidence of locally advanced (nodal or tumor thrombus) or distant (metastatic) disease
• Lesion size (maximal dimension) of 4 to 10 cm
• Patient not a candidate for curative surgery (unwilling or unable to pursue surgery)
• Lesion cannot be reliably treated with ablative techniques
• Entire lesion able to be treated adequately by brachytherapy per radiation oncologist
• Tumor predominantly solid (~ > 80%)
• Lesion that has been observed for >= 6 months with demonstrable growth rate anticipated to be >= 4 mm/year by same imaging modality
• Renal tumor that is amenable to percutaneous access for interstitial renal brachytherapy (Institutional Review Board [IRB])
• Hemoglobin > 9
• Absolute neutrophil count (ANC) >= 1500/uL (microliter)
• Platelets >= 100,000/uL
• Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =< 3.0 upper limit of normal (ULN)
• Total bilirubin =< ULN
• A competent immune system
• Estimated glomerular filtration rate (eGFR) >= 30
• Good performance status (Eastern Cooperative Oncology Group [ECOG]) < 2
• Understanding and willingness to provide consent
• No prior systemic treatment for kidney cancer
• Women of childbearing potential must have negative pregnancy test at start of therapy

Exclusion Criteria

• Presence of an active, untreated, non-renal malignancy
• Uncontrolled medical illness including infections, hypertension, arrhythmias, heart failure, or myocardial infarction within 6 months
• History of bleeding diathesis or recent bleeding episode
• Need for urgent treatment of renal cancer due bleeding, pain, or paraneoplastic syndrome
• Prior surgery or radiation therapy to the operative site
• Unwillingness to undergo clinical and laboratory monitoring and/or imaging studies

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Jonsson Comprehensive Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Albert J Chang

Role: PRINCIPAL_INVESTIGATOR

UCLA / Jonsson Comprehensive Cancer Center

Locations

UCLA / Jonsson Comprehensive Cancer Center

Los Angeles, California, United States

Site Status: RECRUITING

Countries

United States

Facility Contacts

Bashir Wyatt

Role: primary

BAWyatt@mednet.ucla.edu

310-794-3448

Other Identifiers

NCI-2020-04542

Identifier Type: REGISTRY

Identifier Source: secondary_id

19-001258

Identifier Type: -

Identifier Source: org_study_id