Clinical Phase I/II Trial to Investigate Preoperative Dose-Escalated Intensity-Modulated Radiation Therapy (IMRT) and Intraoperative Radiation Therapy (IORT) in Patients With Retroperitoneal Soft Tissue Sarcoma
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 37
- 试验地点
- 2
- 主要终点
- Local Control Rate
研究概览
简要总结
Local control rates in patients with retroperitoneal soft tissue sarcoma (RSTS) remain disappointing even after gross total resection, mainly because wide margins are not achievable in the majority of patients. In contrast to extremity sarcoma, postoperative radiation therapy (RT) has shown limited efficacy due to its limitations in achievable dose and coverage. Although Intraoperative Radiation Therapy (IORT) has been introduced in some centers to overcome these dose limitations and resulted in improved outcome, local failure rates are still high even if considerable treatment related toxicity is accepted. As postoperative administration of RT has some general disadvantages, neoadjuvant approaches could offer benefits in terms of dose escalation, target coverage and reduction of toxicity, especially if highly conformal techniques like intensity-modulated radiation therapy (IMRT) are considered.
Therefore the RETROWTS trials has been designed as a prospective, one armed, single center phase I/II study investigating a combination of neoadjuvant dose-escalated IMRT (50-56 Gy) followed by surgery and IORT (10-12 Gy) in patients with at least marginally resectable RSTS. The primary objective is the local control rate after five years. Secondary endpoints are progression-free and overall survival, acute and late toxicity, surgical resectability and patterns of failure. The aim of accrual is 37 patients in the per-protocol population.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •written informed consent
- •histologically confirmed, primary or locally recurrent soft tissue sarcoma of the retroperitoneal space
- •judged as at least marginally resectable
- •absence of distant metastases
- •tumor size ≥ 5 cm
排除标准
- •missing written informed consent
- •missing histological confirmation of soft tissue sarcoma
- •Desmoid tumor (syn. aggressive fibromatosis)
- •judged as gross incomplete or not resectable
- •incomplete staging
- •presence of distant metastases
- •prior radiation therapy to the abdominal region
- •participation in another clinical interventional study
- •inflammatory bowel disease
结局指标
主要结局
Local Control Rate
时间窗: 5 year
次要结局
- Overall Survival(up to five years from first day of treatment)
- Progression free survival(up to 5 years from first day of treatment)
- Late Toxicity(up to 5 years after first day of treatment)
- Severe acute gastrointestinal toxicity(up to 3 months from first day of treatment)
- Acute toxicity(up to 3 months from first day of treatment)
研究者
Juergen Debus
Prof. Dr. Dr.
University Hospital Heidelberg
