RecruitingPhase 1NCT02811523

In Vivo Lung Perfusion for Pulmonary Metastases of Sarcoma

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


Sponsor

University Health Network, Toronto

Enrollment

17 participants

Start Date

Feb 1, 2016

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 0 YearsMax Age: 64 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a specialized treatment called isolated lung perfusion — where chemotherapy is delivered directly into one lung at a time — for patients with a type of bone or soft tissue cancer called sarcoma that has spread to both lungs. **You may be eligible if...** - You have been diagnosed with soft tissue sarcoma or bone sarcoma - The cancer has spread to both lungs with at least 3 lung spots in total - You are between 18 and 64 years old - You are reasonably active and able to care for yourself - The cancer has not spread outside the lungs - The lung spots can be removed with limited surgery **You may NOT be eligible if...** - You have previously received a very high cumulative dose of the chemotherapy drug doxorubicin - Your heart's pumping strength is below 50% - You have a significant history of serious lung disease - You are pregnant or breastfeeding - You are 65 years or older, or under 18 - You are unable to understand and sign the consent form Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGDoxorubicin

Doxorubicin by In Vivo Lung Perfusion


Locations(1)

Princess Margaret Cancer Centre

Toronto, Canada

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NCT02811523


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