OncoMatch/Clinical Trials/NCT03081910
Autologous T-Cells Expressing a Second Generation CAR for Treatment of T-Cell Malignancies Expressing CD5 Antigen
Is NCT03081910 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies non-drug interventions for t-cell acute lymphoblastic lymphoma.
Patients eligible for this study have a type of blood cancer called T-cell leukemia or lymphoma (lymph gland cancer). The body has different ways of fighting infection and disease. No one way seems perfect for fighting cancers. This research combines two different ways of fighting disease, antibodies and T cells. Antibodies are proteins that protect the body from bacterial and other diseases. T cells, or T lymphocytes, are special infection-fighting blood cells that can kill other cells including tumor cells. Both antibodies and T cells have shown promise treating patients with cancers, but have not been strong enough to cure most patients. T lymphocytes can kill tumor cells but there normally are not enough of them. Some researchers have taken T cells from a person's blood, grown more in the lab then given them back to the person. In some patients who've had recent bone marrow or stem cell transplant, the number of T cells in their blood may not be enough to grow in the lab. In this case, T cells may be collected from their previous transplant donor, who has a similar tissue type. The antibody used in this study, called anti-CD5, first came from mice that have developed immunity to human leukemia. This antibody sticks to T-cell leukemia or lymphoma cells because of a substance on the outside of these cells called CD5. CD5 antibodies have been used to treat people with T-cell leukemia and lymphoma. For this study, anti-CD5 has been changed so that instead of floating free in the blood it is now joined to the T cells. When an antibody is joined to a T cell in this way it is called a chimeric receptor. In the lab, investigators have also found that T cells work better if stimulating proteins, such as one called CD28, are also added. Adding the CD28 makes the cells grow better and last longer in the body, giving them a better chance of killing the leukemia or lymphoma cells. In this study investigators will attach the CD5 chimeric receptor with CD28 added to it to the patient's T cells or the previous bone marrow transplant donor's T cells. The investigators will then test how long the cells last. The decision to use the bone marrow transplant donor's T cells instead of the patient's will be based on 1) whether there is an available and willing donor and 2) the likelihood of the patient's T cells being able to grow in the lab. These CD5 chimeric receptor T cells with CD28 are investigational products not approved by the FDA. UPDATE: Please note that the Autologous Arm of this study is now closed.
Check if I qualifyExtracted eligibility criteria
Cancer type
Acute Lymphoblastic Leukemia
Non-Hodgkin Lymphoma
Biomarker criteria
Required: CD5 overexpression (>50% CD5+ blasts by flow cytometry or immunohistochemistry)
CD5-positive tumor. >50% CD5 + blasts by flow cytometry or immunohistochemistry (tissue) assessed by a CLIA certified Flow Cytometry/Pathology laboratory.
Prior therapy
Must have received: allogeneic hematopoietic stem cell transplant — relapsed post-allogeneic HSCT
Relapsed post-allogeneic HSCT
Cannot have received: investigational agent
Currently receiving any investigational agents or having received any tumor vaccines within the previous 6 weeks
Cannot have received: tumor vaccine
having received any tumor vaccines within the previous 6 weeks
Cannot have received: immunosuppressive treatment for GVHD
Patients who have received Immunosuppressive Treatment (IST) for GVHD within 28 days of infusion
Cannot have received: donor lymphocyte infusion
Patients who have received donor lymphocyte infusion (DLI) within 28 days of infusion
Lab requirements
Blood counts
Hgb ≥ 7.0 g/dL (can be transfused); PT and APTT <1.5x ULN (if pheresis required)
Kidney function
Estimated GFR > 60 mL/min; Creatinine <1.5x ULN (if pheresis required)
Liver function
Bilirubin <3x ULN; AST <5x ULN
Cardiac function
No atrial fibrillation/flutter; No myocardial infarction within last 12 months; No prolonged QT syndrome; Cardiac echocardiography with LVSF ≥30% and LVEF ≥50%; No clinically significant pericardial effusion; No cardiac dysfunction NYHA III or IV
Bilirubin less than 3 times the upper limit of normal. AST less than 5 times the upper limit of normal. Estimated GFR > 60 mL/min. Hgb ≥ 7.0 g/dL (can be transfused). PT and APTT <1.5x ULN (if pheresis required). Cardiac criteria: see exclusion criteria.
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Houston Methodist Hospital · Houston, Texas
- Texas Children's Hospital · Houston, Texas
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