Skip to content

Group study of UFT following instillation of anticancer drug for superficial bladder cancer

Group study of UFT following instillation of anticancer drug for superficial bladder cancer - GUARD study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005596
Enrollment
252
Registered
2011-05-16
Start date
2011-05-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-muscle Invasive Bladder Cancer

Interventions

Treatment arm: Administration of oral UFT 400mg/day for 2 years Control arm: No treatment

Sponsors

University of Tokyo, Department of Urology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Pathologically-proven non-muscle invasive bladder cancer after TUR-Bt with diagnosis of UC, Ta or T1, G1 or G2. Only primary cases are eligible. 2)Treated with immediate instillation of THP (20mg in 20ml saline) after TUR-Bt 3)20-79 year old 4)ECOG Performance Status of 0 or 1 5)Tolerable to oral UFT 6)Life expectancy of > 3 years 7)Reserved organ function 8)Patients who can start protocol therapy within 4 weeks after TUR-Bt 9)Written informed consent

Exclusion criteria

Exclusion criteria: 1)Recurrent cancer 2)UC in prostatic urethra 3)History of previous therapy with UFT or systemic chemotherapy or pelvic radiotherapy 4)Serious comorbidity 5)Contraindication for UFT 6)Women who is pregnant or possibly pregnant 7)Any contraindication investigator specify

Design outcomes

Primary

MeasureTime frame
3 year recurrence-free survival

Countries

Japan

Contacts

Public ContactYutaka Enomoto

University of Tokyo Department of Urology

yenomoto-tky@umin.ac.jp03-5800-8753

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026