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3-Dimensional Conformal Radiation Therapy in Treating Patients With Bladder Cancer Who Have Undergone Transurethral Resection of the Bladder

Image Guided Dose Escalated Adaptive Bladder Radiotherapy

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01124682
Enrollment
60
Registered
2010-05-17
Start date
2009-05-31
Completion date
Unknown
Last updated
2013-08-26

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

Conditions

Bladder Cancer

Keywords

adenocarcinoma of the bladder, squamous cell carcinoma of the bladder, transitional cell carcinoma of the bladder, recurrent bladder cancer, stage II bladder cancer, stage III bladder cancer, stage IV bladder cancer

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. PURPOSE: This phase I trial is studying the side effects and best dose of 3-dimensional conformal radiation therapy in treating patients with bladder cancer who have undergone transurethral resection of the bladder.

Detailed description

OBJECTIVES: Primary * To determine the maximum-tolerated dose of external-beam radiotherapy delivered as a tumor boost in patients who have undergone prior transurethral bladder resection for muscle-invasive carcinoma of the bladder. Secondary * To document progression-free survival and overall survival of these patients. * To evaluate patterns of recurrence and bladder preservation rates following dose-escalated radiotherapy in these patients. * To determine the impact of acute and late toxicity on quality of life in these patients. * To assess the use of gold seeds for tumor boost delineation in these patients. * To evaluate the use of virtual cystoscopy tumor localization in these patients. * To assess coverage of the phase II radiotherapy boost volume on the daily cone-beam images. * To assess coverage of the phase III radiotherapy volume on cone-beam images with selected adaptive strategy. * To evaluate the use of diffusion-weighted MRI (dwMRI) scans in assessing response to radiotherapy. OUTLINE: This is a dose-escalation study. Patients undergo a rigid cystoscopy and gold-seed insertion, if clinically appropriate. Approximately 3-5 seeds are inserted into the bladder wall to demarcate the maximum extent of visible tumor or tumor bed via a customized introducer. All patients undergo 3-dimensional conformal radiotherapy once daily, 5 days per week during weeks 1 and 4-7 and once daily, 4-6 days per week during weeks 2 and 3, using a combination of image-guided radiotherapy techniques and a partial bladder radiotherapy boost. Patients complete quality-of-life questionnaire QOL-30 at baseline, 1 and 3 months, and then annually after completion of study treatment. After completion of study treatment, patients are followed up at 4, 8, and 12 weeks, every 6 months for 3 years, and then annually for 2 years.

Interventions

PROCEDUREdiffusion-weighted magnetic resonance imaging
PROCEDUREquality-of-life assessment
RADIATION3-dimensional conformal radiation therapy

Sponsors

Institute of Cancer Research, United Kingdom
Lead SponsorOTHER

Study design

Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Histologically confirmed invasive bladder carcinoma, including the following cellular types: * Adenocarcinoma * Transitional cell carcinoma * Squamous cell carcinoma * Clinical stage G1-3, pT2a-4 disease * Localized disease * No bone or visceral metastases * No lymph node metastases * Has undergone maximal transurethral resection of the bladder tumor and planning to receive radical radiotherapy PATIENT CHARACTERISTICS: * WHO performance status 0-1 * Hemoglobin \> 10 g/dL * WBC \> 3,000/mm\^3 * Platelet count \> 150,000/mm\^3 * Creatinine \< 120 μmol/L * Bilirubin \< 1.5 times upper limit normal (ULN) * AST \< 1.5 times ULN * Alkaline phosphatase \< 1.5 times ULN * Not pregnant * No inflammatory bowel disease or other significant small bowel disease * Physically fit for radical radiotherapy * No psychological, familial, sociological, or geographical condition potentially hampering compliance with the study protocol and follow-up schedule * No other malignancy within the past 2 years except adequately treated basal cell carcinoma of the skin or adequately treated carcinoma in situ of the cervix uteri * Prior superficial transitional cell carcinoma of the bladder allowed PRIOR CONCURRENT THERAPY: * See Disease Characteristics * No prior pelvic surgery * No bilateral hip replacements compromising accurate radiotherapy planning * No prior radiotherapy to the pelvis

Design outcomes

Primary

MeasureTime frame
Maximum-tolerated dose

Secondary

MeasureTime frame
Tumor boost volumes delineated with and without gold seeds
Dose-volume histogram analysis of PTV2 and PTV3 coverage
Change in diffusion coefficient between pre- and post-radiotherapy dwMRI scans
Quality of life
Overall survival
Bladder preservation rates
Acute and late toxicity and safety profile
Progression-free survival

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026