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临床试验/NCT02811523
NCT02811523招募中1 期

In Vivo Lung Perfusion (IVLP) as an Adjuvant Treatment for Patients Undergoing Surgical Resection of Pulmonary Metastases of Bone and Soft Tissues Sarcomas

University Health Network, Toronto1 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2016年2月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
招募中
入组人数
17
试验地点
1
主要终点
Safety of IVLP at selected dose levels by acute lung injury findings

研究概览

简要总结

Sarcoma which has spread to the lungs is most often treated with surgery. Even with surgery, most patients will not be cured and will die from their disease, probably because of small cancer cells that are present in the lungs at the time of surgery, but cannot be seen or detected. It is for this reason that we are looking for a better treatment. Giving chemotherapy after surgery is generally not recommended because it has significant side effects and no benefit has been proven.

This study is investigating a new technique for delivering chemotherapy directly into the lungs at the time of surgery. Delivering chemotherapy directly to the lungs could potentially kill any microscopic cancer cells that are present in the lungs at the time of surgery, while sparing other major organs in the body from the side effects of chemotherapy. This technique is called In Vivo Lung Perfusion (IVLP). This is a Phase I, non-randomized, dose escalation study that will act as a pilot study for a larger prospective, multicenter, controlled clinical trial. Patients who have bilateral disease will have one lung undergo IVLP and the other lung will remain untreated with the IVLP (the other lung will be treated as current standard of care - either surgery or radiation) as a control lung. The patients will undergo a posterolateral thoracotomy. Lung metastases will be identified by visualization or palpation. After surgical isolation of the lung by proximal control of pulmonary artery and veins, IVLP will be initiated. After 3 hours of IVLP, the lung metastases will be removed in the usual fashion. Patients will be cared for post-surgery according to institutional standards. The patients will be followed for up to 2 years. The primary endpoint is safety. Secondary endpoints include additional safety endpoints and efficacy.

研究设计

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

入排标准

年龄范围
0 Years 至 64 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of Soft Tissue or Osteogenic Sarcoma
  • Presence of bilateral pulmonary metastases
  • 3 or more lung lesions in total
  • Age less than 65 years
  • Absence of extra-pulmonary disease
  • Contralateral disease amenable to surgery or radiation
  • All lung lesions in the lung to be treated with IVLP can be resected with wedge or segmental resections (non-IVLP treated lung will be treated with radiation or surgery 4-12 weeks prior to IVLP)

排除标准

  • Patient has previously received more than 450 mg of doxorubicin
  • Left Ventricular Ejection Fraction <50%
  • History of significant pulmonary disease or pneumonitis
  • Pregnant or lactating females
  • Age 65 years or older, or less than 18 years
  • Inability to understand the informed consent process
  • Hypersenstivity to doxorubicin
  • Current participation in another therapeutic clinical trial
  • Previous lung metastatectomy

研究组 & 干预措施

Doxorubicin 5 mcg/ml

Experimental

Doxorubicin 5mcg/ml by in vivo lung perfusion during surgical resection of pulmonary metastases

干预措施: Doxorubicin (Drug)

Doxorubicin 7 mcg/ml

Experimental

Doxorubicin 7mcg/ml by in vivo lung perfusion during surgical resection of pulmonary metastases

干预措施: Doxorubicin (Drug)

Doxorubicin 9 mcg/ml

Experimental

Doxorubicin 9mcg/ml by in vivo lung perfusion during surgical resection of pulmonary metastases

干预措施: Doxorubicin (Drug)

Doxorubicin 7 mcg/ml - expansion

Experimental

Expansion group at ideal dose

干预措施: Doxorubicin (Drug)

结局指标

主要结局

Safety of IVLP at selected dose levels by acute lung injury findings

时间窗: Up to 2 years

Maximal tolerated dose by using a titration design

时间窗: Up to 2 years

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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