GEMINI: An Open-Label, Single-Arm, Phase II Study of Intraoperative Gemcitabine Intravesical Instillation in Patients Undergoing Radical Nephroureterectomy for Upper Tract Urothelial Carcinoma

Who is this study for? Patients with upper urinary tract urothelial cancer undergoing radical nephroureterectomy
What treatments are being studied? Gemcitabine Hydrochloride
Status: Terminated
Location: See all (4) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This phase II trial studies how well gemcitabine works in preventing urothelial cancer from coming back within the bladder (intravesical recurrence) in patients with upper urinary tract urothelial cancer undergoing radical nephroureterectomy. Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Instilling gemcitabine into the bladder during surgery, may reduce the chance of recurrence of upper urinary tract urothelial cancer.

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

• Clinical diagnosis of localized (clinical American Joint Committee on Cancer \[AJCC\] stage Ta-T4N0M0) low- and high-grade UC of the renal pelvis and/or ureter

• Plan to undergo RNU

• Creatinine \< 2.2 mg/dL (194 mmol/L)

• Hemoglobin \> 9 g/dL

• White blood cell count \>= 3000/uL

• Platelet count \> 75,000/uL and \< 500,000/uL

• Serum bilirubin levels below 2 times the institution's upper limits of normal

• Alkaline phosphatase levels below 2 times the institution's upper limits of normal

• Aspartate aminotransferase levels below 2 times the institution's upper limits of normal

• Alanine aminotransferase levels below 2 times the institution's upper limits of normal

• Eastern Cooperative Oncology Group (ECOG) performance status score 0 - 2

• Suitable candidate for surgery at the discretion of the investigator

• Patient must be capable of giving appropriate approved informed consent or have an appropriate representative available to do

• Patient with a prior malignancy allowed if adequately treated \> 3 years ago with no current evidence of disease

• Women of childbearing potential (WOCBP) must have a negative pregnancy urine test within 28 days of registration, and be using an adequate method of contraception to avoid pregnancy prior to and for at least 6 months after gemcitabine instillation to minimize the risk of pregnancy

• Male patient who has a partner that is a WOCBP must agree to use physician-approved contraceptive methods (e.g., abstinence, condoms, vasectomy) and should avoid conceiving children prior to and for 6 months following gemcitabine instillation

Locations
United States
Florida
Mayo Clinic in Florida
Jacksonville
Minnesota
Mayo Clinic in Rochester
Rochester
North Carolina
Wake Forest Baptist Medical Center
Winston-salem
Pennsylvania
University of Pittsburgh Cancer Institute (UPCI)
Pittsburgh
Time Frame
Start Date: 2020-06-05
Completion Date: 2023-02-02
Participants
Target number of participants: 25
Treatments
Experimental: Prevention (gemcitabine hydrochloride)
Patients receive gemcitabine hydrochloride intravesically for at least 1 hour at the time of RNU.
Sponsors
Leads: Mayo Clinic

This content was sourced from clinicaltrials.gov

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