RecruitingPhase 1NCT04995003

HER2 Chimeric Antigen Receptor (CAR) T Cells in Combination With Checkpoint Blockade in Patients With Advanced Sarcoma

Phase I Study of HER2 Chimeric Antigen Receptor (CAR) T Cells in Combination With Checkpoint Blockade in Patients With Advanced Sarcoma (HEROS 3.0)


Sponsor

Baylor College of Medicine

Enrollment

25 participants

Start Date

Dec 7, 2021

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to learn whether it is safe to give HER2-CAR T cells in combination with an immune checkpoint inhibitor drug (pembrolizumab or nivolumab), to learn what the side effects are, and to see whether this therapy might help patients with sarcoma. Another goal of this study is to study the bacteria found in the stool of patients with sarcoma who are being treated with HER2 CAR T cells and immune checkpoint inhibitor drugs to see if the types of bacteria influence how well the treatment works. The investigators have found from previous research that they can put a new gene into T cells that will make them recognize cancer cells and kill them. They now want to see if they can put a new gene in these cells that will let the T cells recognize and kill sarcoma cells. The new gene that the investigators will put in makes an antibody specific for HER2 (Human Epidermal Growth Factor Receptor 2) that binds to sarcoma cells. In addition, it contains CD28, which stimulated T cells and make them last longer. After this new gene is put into the T cell, the T cell becomes known as a chimeric antigen receptor T cell or CAR T cell. In another clinical study using these CAR T cells targeting HER2 as well as other studies using CAR T cells, investigators found that giving chemotherapy before the T cell infusion can improve the effect the T cells can have. Giving chemotherapy before a T cell infusion is called lymphodepletion since the chemotherapy is specifically chosen to decrease the number of lymphocytes in the body. Decreasing the number of the patient's lymphocytes first should allow the infused T cells to expand in the body, and potentially kill cancer cells more effectively. The chemotherapy used for lymphodepletion is a combination of cyclophosphamide and fludarabine. After the patient receives the lymphodepletion chemotherapy and CAR T cells during treatment on the study, they will receive an antibody drug called an immune checkpoint inhibitor, pembrolizumab or nivolumab. Immune checkpoint inhibitors are drugs that remove the brakes on the immune system to allow it to act against cancer.


Eligibility

Min Age: 1 YearMax Age: 25 Years

Plain Language Summary

Simplified for easier understanding

This study tests a combination of genetically engineered immune cells (HER2-targeted CAR-T cells) and checkpoint immunotherapy drugs (pembrolizumab or nivolumab) in children and young adults with HER2-positive sarcoma (a type of bone or soft tissue cancer) that has grown or returned after prior treatment. **You may be eligible if...** - You are aged 1–25 with HER2-positive sarcoma confirmed by biopsy - Your cancer has progressed or returned after at least one prior systemic treatment - You have reasonable functional ability (Karnofsky/Lansky score ≥60) - You have adequate heart, blood, liver, and kidney function - You are at least 4 weeks out from your last chemotherapy (7 days for targeted drugs) **You may NOT be eligible if...** - You have known HIV - You have active autoimmune disease requiring systemic treatment - You have had a solid organ transplant - You have severe previous reactions to cyclophosphamide or fludarabine - You have active pneumonitis or serious lung inflammation - You are pregnant or breastfeeding - You have a primary immunodeficiency 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

GENETICT cells or CAR T cells

There are 2 dose levels: Dose Level 1 (1x10\^8 cells/m2) and Dose Level -1 (5x10\^7 cells/m2). In the event that Dose Level 1 is not tolerable, de-escalation to Dose Level -1 will occur.

DRUGPembrolizumab Injectable Product

2 mg/kg/dose (max 200 mg/dose) every 3 weeks

DRUGNivolumab Injectable Product

3 mg/kg/dose (\<40kg) or 124 mg (≥40 kg) every 2 weeks


Locations(1)

Texas Children's Hospital

Houston, Texas, United States

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NCT04995003


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