Recurrent Adult Soft Tissue Sarcoma Clinical Trial
Official title:
A Phase I Study To Determine the Feasibility of Using Autologous NY-ESO-1 Specific CD8+ T Cells For the Treatment of Patients With Advanced Myxoid/ Round Cell Liposarcoma and Synovial Sarcoma.
This phase I trial studies the side effects and how well giving autologous T cells with cyclophosphamide works in treating patients with soft tissue sarcoma that is metastatic or cannot be removed by surgery. Biological therapies, such as cellular adoptive immunotherapy, may stimulate the immune system in different ways and stop cancer cells from growing. Drugs used in chemotherapy, such as cyclophosphamide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving autologous T cells together with cyclophosphamide may kill more tumor cells.
PRIMARY OBJECTIVES:
I. Assess the feasibility, safety and toxicity of treating patients with NY-ESO-1 specific
cellular adoptive immunotherapy in myxoid/round cell liposarcoma (MRCL) and synovial sarcoma
patients receiving autologous cluster of differentiation (CD)8+ NY-ESO-1 specific T cells
following cyclophosphamide conditioning.
SECONDARY OBJECTIVES:
I. Evaluate the antitumor effect and persistence of adoptively transferred CD8+
antigen-specific cytotoxic T lymphocyte (CTL) lines following cyclophosphamide conditioning.
OUTLINE:
Patients receive cyclophosphamide intravenously (IV) on days -3 and -2. Patients receive
NY-ESO-1-specific T cells IV on day 0.
After completion of study treatment, patients are followed up for 8 weeks.
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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