EUCTR2009-014264-19-FR进行中(未招募)不适用
Prospective multicentric evaluation of a bladder preservation strategy using a combination of neoadjuvant chemotherapy with intensified MVAC (Méthotrexate + vinblastine + adriamicine + Cisplatine) and optimal bladder transurethral resection in patients with a localized muscle infiltrative urothelial carcinoma (protocol ReChiVe) - ReChiVe
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •T2 clinical stage (no palpable mass under anesthesia after TURB)
- •Absence of diffuse Cis (Cis on random bladder biopsies)
- •Patients above 18, and below 75 years of age
- •PS status = 1
- •No previous treatment for a bladder muscle infiltrative carcinoma. Previous endovesical instillations for non muscle infiltrative lesions (pTa, pT1, Cis) are allowed.
- •No metastases on thoraco-abdomino-pelvic CT scan (no node > 1 cm) and bone scan.
- •Normal biological values: neutrophils > 1,5.109 /l, platellets > 100. 109 /l, Alcaline Phosphatases < 2 x N, bilirubine < 1,5 N, Transaminases < 1,5 x N, Créatinine clairance = 60 ml/min
- •Signed inform consent
- •Patient belonging to a social security system.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •All other histologia than urothelial carcinoma:
- •- primitive adenocarcinoma
- •- epidermoid carcinoma
- •- little cells carcinoma
- •In situ diffuse carcinoma associated with urothelial carcinoma muscular infiltrating
- •Tumor stade > T2, T3 or T4 or pT4a (prostatis)
- •Serious cardiac, pulmonary, hepathitic, renal, digestive or neurological pathology which is non equilibrating or potenbtial aggravating risk by treatment
- •Cancer history or other actual cancer (exept skin cancer) not remission or with an end of treatment inferior to 2 years
- •Participation to another clinical trial in a delay inferior to 30 days
研究者
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