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Clinical Trial Summary

This phase II trial studies how well nivolumab works in treating patients with human T-cell leukemia virus (HTLV)-associated T-cell leukemia/lymphoma. Nivolumab is an antibody, which is a type of blood protein that tags infected cells and other harmful agents. Nivolumab works against a protein called programmed cell death (PD)-1 and may help the body destroy cancer cells by helping the immune system to keep fighting cancer.


Clinical Trial Description

PRIMARY OBJECTIVES: I. To determine the safety and tolerability of nivolumab for patients with HTLV-associated adult T-cell leukemia lymphoma (ATLL). II. To determine the efficacy of nivolumab for patients with HTLV-associated ATLL. SECONDARY OBJECTIVES: I. To determine effects of nivolumab on HTLV-1 proviral deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) loads. II. To determine the effects of nivolumab on anti-HTLV-1 and anti-ATLL immune responses. III. To determine effects of nivolumab on HTLV-1 integration site clonality. OUTLINE: Patients receive nivolumab intravenously (IV) over 60 minutes on day 1. Treatment repeats every 14 days for 46 courses in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up every 3 months for 1 year. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02631746
Study type Interventional
Source National Cancer Institute (NCI)
Contact
Status Completed
Phase Phase 2
Start date February 21, 2017
Completion date March 30, 2018

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