In Vivo Lung Perfusion for Pulmonary Metastases of Sarcoma
Primary Purpose
Bone Sarcoma, Soft Tissue Sarcoma, Pulmonary Metastases
Status
Recruiting
Phase
Phase 1
Locations
Canada
Study Type
Interventional
Intervention
Doxorubicin
Sponsored by
About this trial
This is an interventional treatment trial for Bone Sarcoma
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of Soft Tissue or Osteogenic Sarcoma
- Presence of bilateral pulmonary metastases
- 3 or more lung lesions in total
- Age less than 65 years
- ECOG 0-2
- 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)
Exclusion Criteria:
- 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
Sites / Locations
- Princess Margaret Cancer CentreRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
Experimental
Experimental
Arm Label
Doxorubicin 5 mcg/ml
Doxorubicin 7 mcg/ml
Doxorubicin 9 mcg/ml
Doxorubicin 7 mcg/ml - expansion
Arm Description
Doxorubicin 5mcg/ml by in vivo lung perfusion during surgical resection of pulmonary metastases
Doxorubicin 7mcg/ml by in vivo lung perfusion during surgical resection of pulmonary metastases
Doxorubicin 9mcg/ml by in vivo lung perfusion during surgical resection of pulmonary metastases
Expansion group at ideal dose
Outcomes
Primary Outcome Measures
Safety of IVLP at selected dose levels by acute lung injury findings
Maximal tolerated dose by using a titration design
Secondary Outcome Measures
Full Information
NCT ID
NCT02811523
First Posted
June 21, 2016
Last Updated
May 12, 2023
Sponsor
University Health Network, Toronto
1. Study Identification
Unique Protocol Identification Number
NCT02811523
Brief Title
In Vivo Lung Perfusion for Pulmonary Metastases of Sarcoma
Official Title
In Vivo Lung Perfusion (IVLP) as an Adjuvant Treatment for Patients Undergoing Surgical Resection of Pulmonary Metastases of Bone and Soft Tissues Sarcomas
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 2016 (Actual)
Primary Completion Date
February 2025 (Anticipated)
Study Completion Date
February 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bone Sarcoma, Soft Tissue Sarcoma, Pulmonary Metastases
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Sequential Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
17 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Doxorubicin 5 mcg/ml
Arm Type
Experimental
Arm Description
Doxorubicin 5mcg/ml by in vivo lung perfusion during surgical resection of pulmonary metastases
Arm Title
Doxorubicin 7 mcg/ml
Arm Type
Experimental
Arm Description
Doxorubicin 7mcg/ml by in vivo lung perfusion during surgical resection of pulmonary metastases
Arm Title
Doxorubicin 9 mcg/ml
Arm Type
Experimental
Arm Description
Doxorubicin 9mcg/ml by in vivo lung perfusion during surgical resection of pulmonary metastases
Arm Title
Doxorubicin 7 mcg/ml - expansion
Arm Type
Experimental
Arm Description
Expansion group at ideal dose
Intervention Type
Drug
Intervention Name(s)
Doxorubicin
Intervention Description
Doxorubicin by In Vivo Lung Perfusion
Primary Outcome Measure Information:
Title
Safety of IVLP at selected dose levels by acute lung injury findings
Time Frame
Up to 2 years
Title
Maximal tolerated dose by using a titration design
Time Frame
Up to 2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
0 Years
Maximum Age & Unit of Time
64 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of Soft Tissue or Osteogenic Sarcoma
Presence of bilateral pulmonary metastases
3 or more lung lesions in total
Age less than 65 years
ECOG 0-2
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)
Exclusion Criteria:
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marcelo Cypel, M.D.
Phone
416-581-7773
Email
marcelo.cypel@uhn.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Jennifer Lister, BSc CCRP
Phone
416-340-4857
Email
Jennifer.Lister@uhn.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marcelo Cypel, MD
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
Princess Margaret Cancer Centre
City
Toronto
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marcelo Cypel, M.D.
Phone
416-581-7773
Email
marcelo.cypel@uhn.ca
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
In Vivo Lung Perfusion for Pulmonary Metastases of Sarcoma
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