EUCTR2004-001347-29-DK进行中(未招募)不适用
Treatment of patients with locally advanced rectal cancer. TEGAFOX (UFT/leukovorin og Oxaliplatin) before, during and after curatively intended radiotherapy. A Danish phase I/II trial - TEGAFOX
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 入组人数
- 60
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
- •- Histologically proven adenocarcinoma of the rectum
- •- Locally advanced (surgically unresectable) or recurrent rectal cancer
- •- Primarily unresectable: fixation of tumor to sacral bone or pelvic wall or invation into pelvic soft tissue (e.g. nerves, blood vessels, bladder, prostate)
- •- WHO perforamnce 0-2
- •- Disease confined to the pelvis
- •- A life expectancy of at least 3 months
- •- Age >18 years
- •-Adequate hematological (White Blood Cell counts (WBC) =3.0 x 109/l and platelets =100 x 109/l), hepatic (bilirubin <1.5 x upper normal limit) and renal (creatinine <150 umol/l) function
- •- Written and oral informed consent of the patient in accordance with the Ethical Committees
- •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
- •- Adjuvant chemotherapy or immunotherapy within 12 months
- •- Previous RT to the pelvic area
- •- Exploratory laparotomy within 4 weeks
- •- Patients with any contraindication to the planned chemotherapy or RT
- •- Other active malignant disease within 5 years except adequately treated basal or squamous cell carcinoma of the skin or in situ carcinoma of the cervix
- •- Other experimental theapy while treated according to this study
研究者
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