ACTRN12620000757910招募中未知
Functional imaging-guided radiotherapy dose escalation in rectal adenocarcinoma: a feasibility study
Dr Myo Min0 个研究点目标入组 30 人开始时间: 2020年7月23日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Able to give informed consent
- •- Histologically-proven primary rectal adenocarcinoma within 0-10cm of anorectal junction on MRI or enteroscopy (T3, T4 or node positive disease with no evidence of metastatic spread (M0) on staging CT-chest/abdomen/pelvis (i.e. stage II/III disease))
- •- Patient undergoing curative intent neoadjuvant radiotherapy +/- chemotherapy
- •-- Neoadjuvant radiotherapy must be first component of neoadjuvant therapy (i.e. no induction course)
- •-- Concurrent chemotherapy can include capecitabine or fluorouracil
排除标准
- •- Contraindication to MRI studies (e.g. significant claustrophobia, incompatible pacemaker/implantable defibrillator, implanted metals)
- •- Patients receiving total neoadjuvant chemotherapy
- •- Significant imaging artefact precluding accurate MRI-guided radiotherapy planning (bilateral hip replacement etc.)
- •- Previous radiotherapy to pelvis
- •- Other malignancy conferring life expectancy of less than 3 years
- •- Pregnancy
- •- Active inflammatory bowel disease
- •- Prior diagnosis of connective tissue disorder
研究者
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