Pulmonary Suffusion in Controlling Minimal Residual Disease in Patients With Sarcoma or Colorectal Metastases

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorRoswell Park Cancer Institute

About this trial

This phase I/II trial studies the side effects of pulmonary suffusion in controlling minimal residual disease in patients with sarcoma or colorectal carcinoma that has spread to the lungs. Pulmonary suffusion is a minimally invasive delivery of chemotherapeutic agents like cisplatin to lung tissues. Drugs used in chemotherapy, such as cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Pulmonary suffusion may also be useful in avoiding later use of drugs by vein that demonstrate no effect on tumors when delivered locally.

Eligibility criteria

Qualifiers

Soft tissue sarcoma

Osteosarcoma

Colorectal carcinoma

Have an Eastern Cooperative Oncology Group (ECOG) performance status of =< 2

Disqualifiers

Participants who have had chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier

Participants with known brain metastases should be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events

Allergy, intolerance, or other serious reaction to chemotherapy drugs that may be used in the procedure

Pregnant or nursing female participants

Trial design

Treatments tested in this trial

  • Cisplatin
  • Isolated Chemotherapeutic Lung Perfusion
  • Metastasectomy

Treatment groups

99 Participants
are divided into 1 treatment group

Sponsors and collaborators