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临床试验/NCT01474356
NCT01474356已完成3 期

HDR Brachytherapy Combined With Interstitial Hyperthermia 500 kHz in Locally Advanced Cervical Cancer Patients. A Prospective Clinical Trial

Maria Sklodowska-Curie National Research Institute of Oncology2 个研究点 分布在 1 个国家目标入组 224 人开始时间: 2006年11月最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
224
试验地点
2
主要终点
LC

研究概览

简要总结

The aim of this randomised trial was to investigate whether hyperthermia (HT) combined with interstitial brachytherapy (ISBT) has any influence on local control (LC), disease-free survival (DFS), or acute and late side effects in patients with advanced cervical cancer. Vaginal symptoms were assessed by SOMA score, bladder and rectum symptoms by EORTC/RTOG score. Following the completion of radiochemotherapy, consecutive patients with cervical cancer (FIGO stage II - III) were randomly assigned to two treatment groups, either ISBT alone or ISBT combined with interstitial hyperthermia (ISHT). A total of 205 patients were included in the statistical analysis. Once a week, HT, at a temperature above 42.5°C, was administered for 45 minutes before and during the HDR BT. Follow-up examinations were scheduled at 6 weeks after the completion of BT, every 3 months during the first 2 years, and every 6 months throughout the next 3 years. If relapse was suspected, biopsies were obtained from these patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • patients with locally advanced cervical cancer FIGO stage II - III
  • signed informed consent for participation in the study

排除标准

  • patients with FIGO stage I and IV
  • patients with poor performance status with contraindications for radical treatments

结局指标

主要结局

LC

时间窗: Follow up was scheduled every 3 months. Preliminary results after 3 years.

When local relapse was suspected, biopsy was obtained.

次要结局

  • Early complications of BT procedure(24 hours after BT procedure)
  • Late side effects(Follow up was scheduled every 3 months. Preliminary results after 3 years.)
  • DFS(Follow up was scheduled every 3 months. Preliminary results after 3 years.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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