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NCT Number: NCT02811523

In Vivo Lung Perfusion for Pulmonary Metastases of Sarcoma

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.

Recruiting

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Key information

Age range

0 year–64 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Princess Margaret Cancer Centre

Toronto, Canada

Location status: Recruiting

Location contact

Marcelo Cypel, M.D.

CONTACT

[email protected]

416-581-7773

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Doxorubicin

Drug

Doxorubicin by In Vivo Lung Perfusion

Primary outcomes

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

    Time frame: Up to 2 years

  2. Maximal tolerated dose by using a titration design

    Time frame: Up to 2 years

Study contacts

Contact information is provided by the study sponsor or research team.

Jennifer Lister, BSc CCRP

CONTACT

[email protected]

416-340-4857

Marcelo Cypel, M.D.

CONTACT

[email protected]

416-581-7773

Sponsors and collaborators

Lead sponsor

University Health Network, Toronto

Other

Registry information

Official study title

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

Important dates

Study start
2016
Primary completion
2030
Study completion
2030
First posted
Jun 23, 2016
Registry last updated
Nov 26, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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