Recurrent Merkel Cell Carcinoma Clinical Trial
Official title:
Viral Oncoprotein Targeted Autologous T Cell Therapy for Merkel Cell Carcinoma
This phase I/II trial studies the side effects and best way to give laboratory treated autologous T cells together with aldesleukin and to see how well it works in treating patients with merkel cell carcinoma that has spread from the primary site (place where it started) to other places in the body. Biological therapies, such as cellular adoptive immunotherapy, may stimulate the immune system in different ways and stop tumor cells from growing. Aldesleukin may stimulate the white blood cells to kill tumor cells. Giving cellular adoptive immunotherapy with aldesleukin may be a better treatment for metastatic merkel cell carcinoma.
PRIMARY OBJECTIVES:
I. Determine the safety and potential toxicities associated with treating patients with
metastatic merkel cell carcinoma (MCC) by combined myosin heavy chain (MHC) up-regulation
therapy and adoptive transfer of merkel cell polyomavirus (MCPyV) T-antigen (TAg)-specific
polyclonal autologous cluster of differentiation (CD)8+ T cells.
II. Determine the antitumor efficacy associated with treating patients with metastatic MCC
by combined MHC up-regulation therapy and adoptive transfer of MCPyV TAg-specific polyclonal
autologous CD8+ T cells.
SECONDARY OBJECTIVES:
I. Determine the in vivo persistence and where evaluable, migration to tumor sites of
adoptively transferred polyclonal CD8+ T cells targeting the MCPyV TAg.
II. Determine the in vivo functional capacity of adoptively transferred polyclonal CD8+ T
cells targeting the MCPyV TAg.
OUTLINE:
Patients undergo radiation therapy or recombinant interferon beta intralesional injection
within day -3 to day -1.
Patients receive MCPyV TAg-specific polyclonal autologous CD8-positive T cell vaccine
intravenously (IV) on day 1 and aldesleukin subcutaneously (SC) every 12 hours on days 1-14.
Treatment repeats at least every 28 days for up to 2 courses in the absence of disease
progression or unacceptable toxicity.
Patients with continued presence of detectable metastatic disease 8 weeks after the first
infusion may repeat the treatment regimen including radiation therapy or recombinant
interferon beta injection.
After completion of study treatment, patients are followed up every 3 months.
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Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
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QUILT-3.009: Patients With Stage III (IIIB) or Stage (IV) Merkel Cell Carcinoma (MCC)
|
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