RecruitingPhase 1NCT04815356

Phase I Study of Anti-CD22 Chimeric Receptor T Cells in Patients With Relapsed/Refractory Hairy Cell Leukemia and Variant


Sponsor

National Cancer Institute (NCI)

Enrollment

27 participants

Start Date

May 23, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Background: CAR (Chimeric Antigen Receptor) T cell therapy is a type of cancer treatment in which a person s T cells (a type of immune cell) are changed in a laboratory to recognize and attack cancer cells. Researchers want to see if this treatment can help people with hairy cell leukemia (HCL). Objective: To test whether it is safe to give anti-CD22 CAR T cells to people with HCL. Eligibility: Adults ages 18 and older with HCL (classic or variant type) who have already had, are unable to receive, or have refused other standard treatments for their cancer. Design: Participants will be screened with the following: Medical history Physical exam Blood and urine tests Biopsy sample Electrocardiogram Echocardiogram Lung function tests Imaging scans Some screening tests will be repeated during the study. Participants may need to have a catheter placed in a large vein. Participants will have magnetic resonance imaging of the brain. Participants will have a neurologic evaluation and fill out questionnaires. Participants will have leukapheresis. Blood will be removed from the participant. A machine will divide whole blood into red cells, plasma, and lymphocytes. The lymphocytes will be collected. The remaining blood will be returned to the participant. Participants will get infusions of chemotherapy drugs. Participants will get an infusion of the anti-CD22 CAR T cells. They will stay at the hospital for 14 days. Then they will have visits twice a week for 1 month. After treatment, participants will be followed closely for 6 months, and then less frequently for at least 5 years. Then they will have long-term follow-up for 15 years.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This early-phase study is testing a new type of immune cell therapy (called CAR-T cells) that targets a protein called CD22, which is found on certain cancer cells. It is designed for people with hairy cell leukemia (HCL) — a rare, slow-growing blood cancer — whose disease has come back or stopped responding to treatment. **You may be eligible if...** - You have been diagnosed with hairy cell leukemia or a related variant (HCLv), confirmed by a specialist - Your disease has returned or stopped responding to previous treatments - Your cancer is causing low blood counts, an enlarged spleen, or other complications that need treatment **You may NOT be eligible if...** - You do not have a confirmed HCL or HCLv diagnosis - Your cancer is not causing symptoms that meet the criteria for treatment - You have certain other active serious health conditions Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BIOLOGICALCD22CART cell infusion

The treatment regimen will consist of lymphodepleting chemotherapy followed by CD22CART infusion: Days -4 to -2: fludarabine 25 mg/m2/dose Day -2: cyclophosphamide 900 mg/m2/dose Day 0: CD22CART infusion (starting at dose level 1 \[DL1\]: 1 x 105 transduced CAR-T cells/kg) on Day 0 participants will be evaluated for response at Day 28 post-CD22CART infusion.


Locations(1)

National Institutes of Health Clinical Center

Bethesda, Maryland, United States

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NCT04815356


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