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Clinical Trials/NCT00981656
NCT00981656
Completed
Phase 2

A Phase II Protocol for Patients With Stage T1 Bladder Cancer to Evaluate Selective Bladder Preserving Treatment by Radiation Therapy Concurrent With Radiosensitizing Chemotherapy Following a Thorough Transurethral Surgical Re-Staging

Radiation Therapy Oncology Group13 sites in 1 country37 target enrollmentNovember 2009

Overview

Phase
Phase 2
Intervention
cisplatin
Conditions
Bladder Cancer
Sponsor
Radiation Therapy Oncology Group
Enrollment
37
Locations
13
Primary Endpoint
Percentage of Participants Free From Radical Cystectomy at 3 Years
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. Drugs used in chemotherapy, such as cisplatin, mitomycin C, and fluorouracil, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving radiation therapy together with cisplatin may kill more tumor cells.

PURPOSE: This phase II trial is studying how well radiation therapy given together with chemotherapy works in treating patients with stage I bladder cancer.

Detailed Description

After completion of study treatment, patients are followed up every 3 months for 1 year, every 4 months for 1 year, every 6 months for 3 years, and annually thereafter until termination of the study.

Registry
clinicaltrials.gov
Start Date
November 2009
End Date
August 15, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

3DCRT + CT

Concurrent three-dimensional conformal radiation therapy (3DCRT) and radiosensitizing chemotherapy (CT) consisting of either cisplatin alone or the combination of mitomycin and 5-fluorouracil. Protocol treatment must begin with 15 weeks after a transurethral resection of the tumor (TURBT).

Intervention: cisplatin

3DCRT + CT

Concurrent three-dimensional conformal radiation therapy (3DCRT) and radiosensitizing chemotherapy (CT) consisting of either cisplatin alone or the combination of mitomycin and 5-fluorouracil. Protocol treatment must begin with 15 weeks after a transurethral resection of the tumor (TURBT).

Intervention: 5-fluorouracil

3DCRT + CT

Concurrent three-dimensional conformal radiation therapy (3DCRT) and radiosensitizing chemotherapy (CT) consisting of either cisplatin alone or the combination of mitomycin and 5-fluorouracil. Protocol treatment must begin with 15 weeks after a transurethral resection of the tumor (TURBT).

Intervention: Mitomycin

3DCRT + CT

Concurrent three-dimensional conformal radiation therapy (3DCRT) and radiosensitizing chemotherapy (CT) consisting of either cisplatin alone or the combination of mitomycin and 5-fluorouracil. Protocol treatment must begin with 15 weeks after a transurethral resection of the tumor (TURBT).

Intervention: Three-Dimensional Conformal Radiation Therapy

Outcomes

Primary Outcomes

Percentage of Participants Free From Radical Cystectomy at 3 Years

Time Frame: Three years from registration

The number of participants who did not undergo a radical cystectomy within three years divided by the number of analyzed participants, presented with the 97.5% lower bound.

Secondary Outcomes

  • Percentage of Participants With Progression to Tumor Stage T2 or Greater at 5 Years(From registration to five years)
  • Percentage of Participants Free From Radical Cystectomy at 5 Years(Five years from registration)
  • Percent of Participants With Distant Disease Progression at 5 Years(From registration to five years)
  • Percent of Participants With Distant Disease Progression at 3 Years(From registration to three years)
  • Percentage of Participants Alive at 5 Years(From registration to five years)
  • Distribution of Participants by Highest Grade Adverse Event(Adverse events are evaluated 8-10 weeks after end of study treatment (approximately 7 weeks), then every 3 months for one year, every 4 months for one year, every 6 months for 3 years, then annually. Maximum follow-up at time of reporting was 8.6 years.)
  • American Urological Association Total Symptom Score at Baseline and at 3 Years(Baseline and 3 years)
  • Percentage of Participants With Progression to Tumor Stage T2 or Greater at 3 Years(From registration to three years)
  • Percentage of Participants Alive at 3 Years(From registration to three years)
  • Percentage of Participants Who Have Died From Bladder Cancer at 5 Years (Disease-specific Survival)(From registration to five years)
  • Percentage of Participants With Local Recurrence at 3 Years(From registration to three years)

Study Sites (13)

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