Adoptive Immunotherapy With Activated Marrow Infiltrating Lymphocytes and Cyclophosphamide Graft-Versus-Host Disease Prophylaxis in Patients With Relapse of Hematologic Malignancies After Allogeneic Hematopoietic Cell Transplantation

Overview

This Phase 1 clinical study is designed to examine the safety and feasibility of using anti-CD3/CD28 activated marrow infiltrating lymphocytes (MILs) as treatment of relapse after allogeneic hematopoietic cell transplantation (alloHCT) for patients with hematologic malignancies with bone marrow involvement of their relapsed disease. 

SparkCures ID 857
Trial Phase Phase 1
Enrollment 27 Patients
Treatments
  • T Cells
Tags
Trial Sponsors
  • Sidney Kimmel Comprehensive Cancer Center
Trial Collaborators
  • National Cancer Institute (NCI)
NCT Identifier

NCT02342613

CLOSED

This trial is active but is no longer accepting patients.

Am I Eligible?

The following criteria is a partial list of reasons why patients may or may not be eligible to participate in this clinical trial. Further evaluation with a medical professional will be required to determine full eligibility.

The following criteria is provided for health care professionals.

Inclusion Criteria:

  • Age ≥18 years old
  • Bone marrow relapse of a hematologic malignancy ≥6 months after alloHCT using PTCy
  • Donor CD3+ chimerism ≥ 30% measured in peripheral blood or bone marrow
  • ECOG performance status ≤ 2 or Karnofsky performance scale ≥ 70%.
  • Off all immunosuppressive drugs for 2 weeks prior to the PTCy-MILs collection.
  • Expectation of ability to safely undergo salvage treatment appropriate for the patient's malignant disease type as determined by the treating hematologist/ oncologist.

Exclusion Criteria:

  • Most recent alloHCT not utilizing PTCy.
  • Active GVHD requiring treatment.
  • Immunosuppression use within 28 days of PTCy-MIL infusion if prior grade II-IV acute GVHD.
  • Creatinine ≥ 2.5, total bilirubin > 3 times the upper limit of normal (ULN), or AST/ALT > 3 times the ULN.
  • HIV-1/2 or HTLV-1/2 positivity.
  • Life expectancy ≤ 90 days even with aggressive treatment, as determined by the treating hematologist/oncologist, which would preclude assessment of toxicity of PTCy-MILs

US Trial Locations

Please visit the ClinicalTrials.gov page for historical site information.

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