NKG2D.Zeta-NK Cell Conditioning With C7R.GD2.CAR-T Cells for Patients With Relapsed or Refractory Osteosarcoma or Neuroblastoma

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age1-24
SponsorBaylor College of Medicine

About this trial

The purpose of this study is to find the largest safe dose of i15.NKG2D.zeta-NK cells in combination with C7R.GD2.CAR-T cells, and additionally to evaluate how long they can be detected in patients' blood and what affect they have on patients' cancer.

Patients eligible for this study have neuroblastoma or osteosarcoma that expresses a substance on the cancer cells called GD2. This cancer has either come back after treatment or did not respond to the standard or other investigational treatments or therapies used to treat it. There is no standard treatment for these types of advanced cancers at this time. This is a gene transfer research study using special immune cells called NK cells and T cells. NK cells and T cells are types of white blood cell that help the body fight infection.

The body has different ways of fighting infection and disease. No single way seems perfect for fighting cancers. This research study combines two different ways of fighting cancer: NK cells and T cells. T cells are special infection-fighting blood cells that can kill cells infected with viruses and tumor cells. NK cells, another kind of infection-fighting cell, can recognize a wide range of cells in distress, including tumor cells and cells that help protect tumor cells in the cancer environment. Both NK cells and T cells have been used individually to treat patients with cancers. They have shown promise, but have not been strong enough individually to cure most patients.

Investigators have found from previous research that we can put a new gene into T cells that will make them recognize GD2, a substance found on almost all neuroblastoma and osteosarcoma cells. We can also put a new gene into NK cells that help them fight the tumor environment. Investigators know that T cells and NK cells need substances called cytokines to survive but the cells do not get enough cytokines after infusion into the body; therefore, the investigators have added the genes C7R and IL15 into the T and NK cells, respectively, to give each cell a constant supply of cytokine that helps them to survive longer.

The C7R.GD2.CAR-T cells and i15.NKG2D.zeta-NK cells are investigational products not approved by the Food and Drug Administration.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with Neuroblastoma that have persistent disease after standard treatment or have relapsed/refractory disease.

Karnofsky/Lansky score of 60% or greater.

Informed consent and assent (as applicable) obtained from parent/guardian and child.

Greater than 1 year of age.

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • i15.NKG2D.zeta NK cells and C7R.GD2.CARTs cells

    Genetic

    Dose Level 1: 3 x 10\^8/m\^2 of i15.NKG2D.zeta NK cells and 3 x 10\^7/m\^2 of C7R.GD2.CAR T cells given 5 days later.

  • i15.NKG2D.zeta NK cells and C7R.GD2.CARTs cells

    Genetic

    Dose Level 2: 6 x 10\^8/m\^2 of i15.NKG2D.zeta NK cells and 3 x 10\^7 cells/m\^2 of C7R.GD2.CAR T cells given 5 days later.

  • i15.NKG2D.zeta NK cells and C7R.GD2.CARTs cells

    Genetic

    Dose Level 3: 12 x 10\^8/m\^2 of i15.NKG2D.zeta NK cells and 3 x 10\^7 cells/m\^2 of C7R.GD2.CAR T cells given 5 days later.

Treatment groups

27 Participants
are divided into 1 treatment group
Group A: i15.NKG2D.zeta NK cells and C7R.GD2.CARTs cellsExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Dose-limiting toxicity (DLT) rate

Proportion of participants with DLTs related to the combination of NK cell and T cell infusions evaluated as per the NCI CTCAE v5.0 criteria

Time frame
4 weeks post-CAR-T cell infusion
2

Maximum tolerated dose (MTD) of i15.NKG2D.zeta-NK cells when given in combination with C7R.GD2.CAR-T cells

The dose level of infused NK cells for which the DLT rate is approximately 0.3

Time frame
4 weeks post CAR-T infusion of the last participant

Secondary outcomes

1

Objective response rate (ORR)

Proportion of participants with complete response (CR) or partial response (PR) according to RECIST v1.1 criteria and/or MIBG evaluation (for neuroblastoma)

Time frame
6 weeks after CAR-T infusion
2

Cytokine release syndrome (CRS) grade

Any grade CRS as evaluated by established clinical CRS Grading Scale

Time frame
4 weeks post CAR-T infusion

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Baylor College of Medicine

Lead sponsor

Center for Cell and Gene Therapy, Baylor College of Medicine

Collaborator