Renal Cell Carcinoma (RCC) Clinical Trials

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Prospective Study of Interstitial Brachytherapy for Unresectable/Unablatable T1b/T2a Renal Masses

Who is this study for? Patients with kidney cancer that have refused or are unable to undergo surgery or ablation
What treatments are being studied? Interstitial Radiation Therapy
Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Phase 1
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ 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

Locations
United States
California
UCLA / Jonsson Comprehensive Cancer Center
RECRUITING
Los Angeles
Time Frame
Start Date: 2020-07-16
Estimated Completion Date: 2027-06-30
Participants
Target number of participants: 17
Treatments
Experimental: 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.
Related Therapeutic Areas
Sponsors
Leads: Jonsson Comprehensive Cancer Center

This content was sourced from clinicaltrials.gov