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临床试验/NCT01124682
NCT01124682Unknown1 期

Image Guided Dose Escalated Adaptive Bladder Radiotherapy

Institute of Cancer Research, United Kingdom2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2009年5月1日最近更新:
适应症

试验速览

阶段
1 期
发起方
入组人数
60
试验地点
2
主要终点
Maximum-tolerated dose

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 未提供

结局指标

主要结局

Maximum-tolerated dose

次要结局

  • Progression-free survival
  • Overall survival
  • Bladder preservation rates
  • Acute and late toxicity and safety profile
  • Quality of life
  • 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

研究者

发起方
Institute of Cancer Research, United Kingdom
申办方类型
Other

研究点 (2)

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