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Effect of Denileukin Diftitox on Immune System in CTCL Patients

Effect of Denileukin Diftitox in T-Regulatory Cells in CTCL Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00254332
Enrollment
10
Registered
2005-11-16
Start date
2005-11-30
Completion date
2007-09-30
Last updated
2015-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cutaneous T-cell Lymphoma, Mycosis Fungoides, Sezary Syndrome

Keywords

Cutaneous T-cell Lymphoma, Sezary Syndrome, Mycosis Fungoides, Denileukin Diftitox

Brief summary

This is a blood and tissue study to determine the effect of the drug called denileukin diftitox on the immune system cells that may be involved in patient response to their cutaneous t-cell lymphoma. Patients who are undergoing standard of care therapy with denileukin diftitox will be invited to participate. Blood and tissue samples will be obtained at baseline, day 5 and day 19 in up to the first 4 cycles of denileukin diftitox.

Detailed description

Although the etiology of CTCL is not fully understood, it is believed to be a malignancy proliferation of a memory T-cell in the context of Th2-type cytokine profile and suppressed cytotoxic T-cell (CTL) immunity. T-regulatory (T-regs) cells may be important in CTCL in the setting of immunotherapy. Removal of T-regs would result in enhanced immune responses in vitro, which may translate into augmentation of the anti-tumor immune response and durable clinical responses in vivo. We propose to evaluate effects of ONTAK on the T-reg cell subset in patients undergoing routine therapy with ONTAK. We will evaluate T-reg subsets in peripheral blood and tumor tissues from the patients both phenotypically using multi-color FACS analysis and confocal microscopy, and functionally in MLRs and ELISpot assays with baseline, day 5 and 19 blood samples in up to four cycles. Completion date provided represents the completion date of the grant per OOPD records

Interventions

None listed

Sponsors

University of Pittsburgh
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 18 and older * diagnosed with CTCL * able and willing to provide informed consent * will be receiving denileukin diftitox per standard guidelines

Exclusion criteria

* prior history of receiving Ontak * pregnancy

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026