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临床试验/NCT01279135
NCT01279135
已完成
3 期

Phase III Randomized Trial of Image Guided Intensity Modulated Radiotherapy (IG-IMRT) and Conventional Radiotherapy for Late Toxicity Reduction After Postoperative Radiotherapy in Ca Cervix.

Tata Memorial Hospital1 个研究点 分布在 1 个国家目标入组 300 人2011年1月1日

概览

阶段
3 期
干预措施
Conventional Radiation
疾病 / 适应症
Cancer Cervix
发起方
Tata Memorial Hospital
入组人数
300
试验地点
1
主要终点
Late bowel toxicity ≥ Grade II
状态
已完成
最后更新
2个月前

概览

简要总结

The study tests Tomtherapy based Image Guided Radiation against conventional radiation techniques for it's ability to reduce long term small bowel toxicity.

详细描述

Postoperative pelvic radiotherapy (+/- chemotherapy) leads to reduction in the risk of local recurrence and improves progression free survival (PFS) in patients with post-operative intermediate and high risk factors following Wertheim's hysterectomy. However, adjuvant external beam radiotherapy and vaginal cuff brachytherapy increase the risk of small bowel toxicity such that patients undergoing external beam pelvic radiotherapy and vaginal cuff brachytherapy may have 15-18% incidence of late RTOG ≥ grade II small bowel toxicity. Phase II studies using new techniques like Intensity Modulated Radiotherapy (IMRT) have reported up to 50% reduction in small bowel doses with up to 30% reduction in ≥ grade II acute toxicity. However, there is no randomized data demonstrating the benefit of highly specific and conformal techniques like image guided (IG)-IMRT in reducing radiation induced small bowel toxicity in patients with cervical cancers. The present study is being proposed to test if use of IG-IMRT with Tomotherapy is associated with reduced small bowel late toxicity

注册库
clinicaltrials.gov
开始日期
2011年1月1日
结束日期
2020年5月5日
最后更新
2个月前
研究类型
Interventional
研究设计
Parallel
性别
Female

研究者

责任方
Principal Investigator
主要研究者

Supriya Sastri (chopra)

Associate Professor

Tata Memorial Hospital

入排标准

入选标准

  • Histopathological diagnosis of carcinoma cervix with postoperative intermediate or high risk features.
  • Age \>18 years.
  • Planned for Wertheim's hysterectomy or has already undergone Wertheim's hysterectomy OR has undergone Simple Hysterectomy with no evidence of residual nodes on MRI/PET imaging+/- confirmatory nodal biopsy.
  • No evidence of paraaortic nodal metastasis.

排除标准

  • History of multiple previous abdominal surgeries placing patient at baseline high risk of bowel toxicity or any other medical condition with baseline bowel movement disorder.
  • Rectal Polyps or extensive hemorrhoids.

研究组 & 干预措施

Conventional RT

Patients in this arm will receive conventional radiation with or without chemotherapy

干预措施: Conventional Radiation

Tomotherapy based IGRT

Patients in this arm will receive Tomotherapy based IGRT with or without chemotherapy

干预措施: Tomotherapy based IGRT

结局指标

主要结局

Late bowel toxicity ≥ Grade II

时间窗: Median follow up of 3 years

Time to event and severity of late bowel toxicity are assessed

次要结局

  • To identify small bowel dose volume characteristics that predict for ≥ Grade II late toxicity(Median follow up of 3 years)
  • To compare quality of life between Tomotherapy vs conventional radiotherapy arm using EORTC QLQ CX24(3 years from completion of accrual)
  • To evaluate acute toxicity difference in two study arms using CTCAE version 3.0(Within 90 days)
  • Preoperative functional imaging features that predict for local and distant recurrence will be identified(3 years after completion of accrual)
  • To compare quality of life between Tomotherapy vs conventional radiotherapy arm using EORTC QLQ C30(3 years from completion of accrual)

研究点 (1)

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