Chemoresection With 4 Weekly Intravesical Instillations Of Mitomycin C Versus Transurethral Resection (TUR) Followed By One Single Immediate Instillation Of Mitomycin C In Single, Small, Papillary Stage Ta, T1 Bladder Tumors: A Prospective Randomized Phase III Trial
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 入组人数
- 58
- 试验地点
- 24
研究概览
简要总结
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Infusing chemotherapy drugs directly into the bladder may kill more cancer cells. It is not yet known if surgery followed by chemotherapy is more effective than chemotherapy alone in treating bladder cancer.
PURPOSE: Randomized phase III trial to compare the effectiveness of chemotherapy alone with that of transurethral resection followed by chemotherapy in treating patients who have bladder cancer.
详细描述
OBJECTIVES:
- Compare the efficacy of chemoresection with 4 weekly intravesical instillations of mitomycin vs transurethral resection followed by 1 instillation of mitomycin in patients with low-risk superficial transitional cell carcinoma of the bladder.
- Compare the disease-free survival of patients treated with these regimens.
- Determine the response rate at 6 weeks in patients treated with chemoresection.
- Determine the percent of patients with tumor at 6 weeks treated with transurethral resection.
- Compare the quality of life of patients treated with these regimens.
- Compare the side effects of these regimens in these patients.
OUTLINE: This is a randomized, multicenter study. Patients are stratified according to disease status (primary vs recurrent) and participating center. Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients undergo chemoresection with intravesical instillation of mitomycin once weekly for 4 weeks.
- Arm II: Patients undergo transurethral resection followed within 1-6 hours by intravesical instillation of mitomycin.
Quality of life is assessed at baseline, at week 1 (arm II only), at week 5 (arm I only), and then at week 6.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 主要目的
- Treatment
入排标准
- 年龄范围
- — 至 80 Years(Child, Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •DISEASE CHARACTERISTICS:
- •Cytologically confirmed solitary primary or recurrent papillary transitional cell carcinoma of the bladder
- •Tumor no greater than 2 cm in diameter
- •Negative urine cytology
- •No suspicious lesions in bladder requiring biopsy
- •No tumors in the prostatic urethra or upper urinary tract
- •No prior history of T1 G3 tumors, muscle invasive tumors (T2 or greater), or carcinoma in situ
- •PATIENT CHARACTERISTICS:
- •80 and under
- •Performance status
- •Life expectancy
- •Not specified
- •Hematopoietic
- •Not specified
- •Not specified
- •Not specified
- •HIV negative
- •No active intractable or uncontrollable bladder infection
- •No urethral strictures that would preclude endoscopic procedures or repeated catheterization
- •No prior or concurrent congenital or acquired immune deficiency syndrome
- •No other prior or concurrent malignancy except cured basal cell skin cancer or intraepithelial cancer of the cervix
- •No prior or concurrent leukemia or Hodgkin's disease
- •No concurrent disease for which general anesthesia is contraindicated
- •No psychological, familial, sociological, or geographical condition that would preclude study compliance
- •Not pregnant or nursing
- •PRIOR CONCURRENT THERAPY:
- •Biologic therapy
- •More than 12 months since prior BCG vaccine
- •Chemotherapy
- •At least 1 year since prior mitomycin
- •Endocrine therapy
- •Not specified
- •Radiotherapy
- •No prior pelvic radiotherapy
- •No prior organ transplant
- •At least 3 months since prior intravesical treatment
排除标准
- 未提供
