NL-OMON56933尚未招募3 期
Adjuvant chemotherapy for prevention of recurrence in patients with detectable ctDNA after surgery in high-risk rectal cancer. - REACT
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 206
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Age >= 18 years
- •WHO performance score 0-1
- •Informed consent for PLCRC with specific consent for additional blood
- •withdrawals and offering of future experimental research
- •Histological confirmed rectal cancer; either treated with neoadjuvant
- •(chemo)radiotherapy, and/or clinical T4 and/or N+ in case no neoadjuvant
- •therapy was administered.
- •Eligible to receive treatment with combination adjuvant chemotherapy
- •(CAPOX/FOLFOX) according to the treating physician
排除标准
- •Another malignancy in previous 5 years, with the exception of treated
- •carcinoma in situ or skin cancer other than melanoma
- •Incomplete primary tumour resection (R1 or R2 resection)
- •Contra-indication for fluoropyrimidines or oxaliplatin
- •Neoadjuvant oxaliplatin based systemic treatment, e.g. treated with the
- •RAPIDO regimen consisting of short course radiotherapy followed by 6 cycles of
- •CAPOX or 9 cycles of FOLFOX prior to surgery
- •Patients with a clinical complete response, who will not undergo surgery.
- •Pregnant and lactating women
研究者
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