KCT0006235尚未招募未知
Oncologic outcome of multimodal treatment strategy with neoadjuvant oxaliplatin-based chemotherapy for obstructive colon cancer after colonoscopic stent decompression: a randomized controlled trial
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 204
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 20?(Year) 至 74?(Year)(—)
- 性别
- All
入选标准
- •i. Age : 20 years old or more and lesser than 75 years old
- •ii. Agreement of this study
- •iii. Clinical stage II or III colon cancer with colonic obstruction which is confirmed by pathologic review and imaging study.
- •iv. Colon cancer located beween distal T colon and Rectosigmoid junction colon which is defined as a tumor above 15cm from anal verge.
- •v. Colonocopic fiding: tumor involving whole circumference of the lumen, impossible to pass endoscope through the tumor
- •vi. SEMS placement
- •vii. no colonic injury and successful decompression of the colon with in 48 hours after SEMS placement.
- •viii. ECOG performance 0-2
- •ix. ASA = 3
- •x. Appropriate function of the vital organ (acceptable liver enzyme and BUN/Cr)
- •xi. Appropriate function of hematopoietic system (platelet =100,000ul, neutrophil =2,000ul)
- •xii. If the patient is female in fertile period, urine hCG test is negative and she has no plan of pregnancy with 6 months after the termiation of whole treatment.
- •xiii. If the patient is male in fertile period, he agrees with contraception during treatment period and 6 months after the termination of whole treatment.
排除标准
- •i. any suspicious distant metastasis
- •ii. any other primary malignant lesion
- •iii. Clinical stage T1or T2 and N0
- •iv. the sign of perforation or severe ischemia requiring ememgency operation
- •v. the complication related to SEMS placement (severe bleeding and perforation after SEMS placement)
- •vi. ASA 4 or more
- •vii. ECOG 3 or more
- •viii. colonic obstruction by benign stricture
- •ix. pregnant woman or woman who is breastfeeding
- •x. the paitents who already enrolled into other study or are taking medicine related to any clinical trial
- •xi. the patients who are taking sorivudine
- •xii. the patients who are taking Tegafur/gimeracil/oteracil
- •xiii. the patietns who have a medical history of hypersensitivity reaction to 5-FU, oxaliplatin, leucovorin,or any medication including platinum.
- •xiv. Inappropriate function of vital organ (impaired renal function, elevated liver enzyme, and so on )
- •xv. Inappropriate function of hematopoietic system (platelet <100,000ul, neutrophil < 2,000ul)
- •xvi. Genetic problem such as galactose intolerance, Lapp lactase deficiency, or glucose-galatose malabsorption)
研究者
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