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

Adoptive Immunotherapy Utilizing Activated Marrow Infiltrating Lymphocytes Derived From Patients With Bone Marrow Relapse of Hematologic Malignancies After Allogeneic Hematopoietic Cell Transplantation Using Post-Transplantation Cyclophosphamide Graft-Versus-Host Disease Prophylaxis.

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. These MILs will be derived from the bone marrow of the relapsed patient who had previously received post-transplantation cyclophosphamide (PTCy) as graft-versus-host disease (GVHD) prophylaxis (PTCy-MILs). A bone marrow aspiration will be performed on the patient to collect ~200ml of marrow for ex vivo expansion. During this expansion process, T cells will be activated and expanded by co-stimulation with anti-CD3/anti-CD28 monoclonal antibodies covalently attached to super-paramagnetic microbeads. Patients will be treated with salvage therapy while this ex vivo expansion is ongoing. After the simultaneous salvage therapy and ex vivo expansion, the activated PTCy-MILs will be reinfused. Patients will be monitored with the primary objective being the feasibility of expanding to targeted dose levels activated PTCy-MILs that do not cause grade III-IV acute GVHD within the first 90 days after PTCy-MIL infusion.

Study Overview

• Status: Completed
• Conditions: Hematologic Malignancies; Graft-Versus-Host Disease
• Intervention / Treatment: Biological: Activated PTCy-MILs

Detailed Description

Primary Objectives:

1. Feasibility of generating activated PTCy-MILs in patients with relapsed disease involving the bone marrow.
2. Toxicity of PTCy-MILs, specifically the rate of grade III-IV acute GVHD within the first 90 days after PTCy-MIL infusion.

Secondary Objectives

1. Determination of an optimal safe dose for PTCy-MILs.
2. Immunologic characterization of the PTCy-MIL product before and after expansion.
3. Immune reconstitution after treatment with PTCy-MILs.
4. Incidence and severity of chronic GVHD.
5. Clinical responses (complete remissions, partial remissions, stable disease) as measured by criteria specific for the particular disease type.
6. Progression-free and overall survival.

• Study Type: Interventional
• Enrollment (Estimated): 27
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • Maryland
    • Baltimore, Maryland, United States, 21231
      • Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

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

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

Experimental: MILs treatment; Patients treated with the activated PTCy-MILs

Biological: Activated PTCy-MILs; The activated PTCy-MILs will be infused through standard blood tubing containing a 170-260 micron filter without an additional leukoreduction filter into a central IV site. Each of the bags will be infused at a rate of approximately 10 ml per minute. The IV line will be flushed with normal saline immediately after completion of PTCy-MILs infusion to ensure that all product has been infused into the patient.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Feasibility of generating activated marrow infiltrating lymphocytes (MILs) from participants previously treated with post-transplantation cyclophosphamide (PTCy) (PTCy-MILs) who have relapsed disease involving the bone marrow	Feasibility is measured as the number of participants who achieve: 1) The successful obtaining of PTCy-MILs; 2) The expansion of PTCy-MILs to at least 70% of the assigned dose level; 3) Successful infusion of PTCy-MILs; 4) The absence of grade III-IV acute graft-versus-host-disease (GVHD) for 90 days after PTCy-MILs infusion. Acute GVHD is defined by the Modified Keystone Criteria.	90 days

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Optimal safe dose for PTCy-MILs	Optimal safe dose is defined as the maximal MILs cell dose that can be expanded in at least 70% of patients at which upon administration does not exacerbate grade III/IV GVHD	90 days
Immunologic characterization of the PTCy-MIL product before and after expansion	Amount of MILs with expression of CD3, CD4, Cd8, CXCR4, CD45RO, CD62L, CD107a, FasL, markers of exhaustion and T-cell inactivation as identified by multi-color flow cytometry and functional studies of alloMILs and T-cell response.	up to 3 years
Number of participants who experience chronic GVHD	Chronic GVHD is defined by National Institutes of Health (NIH) criteria.	up to 2 years post-transplant
Clinical Response	Number of participants with complete remission (CR), partial remission (PR) and stable disease (SD) as assessed by bone marrow examination, CBC with differential, serum chemistries, cytogenetics and disease-specific molecular studies	up to 3 years
Progression-Free Survival	Time from day of PTCy-MILs infustion to progression/relapse of disease or death from any cause, whichever occurs first	up to 3 years
Overall Survival	Time alive from the day of PTCy-MILs infusion to death from any cause	up to 3 years

Collaborators and Investigators

• Sponsor: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
• Collaborators: National Institutes of Health (NIH)
• Investigators: Principal Investigator: Leo Luznik, MD, Sidney Kimmel Cancer Center at Johns Hopkins

Study record dates

Study Major Dates

• Study Start (Actual): May 28, 2015
• Primary Completion (Actual): November 29, 2023
• Study Completion (Actual): March 31, 2024

Study Registration Dates

• First Submitted: January 15, 2015
• First Submitted That Met QC Criteria: January 15, 2015
• First Posted (Estimated): January 21, 2015

Study Record Updates

• Last Update Posted (Actual): April 25, 2024
• Last Update Submitted That Met QC Criteria: April 24, 2024
• Last Verified: April 1, 2024

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Immune System Diseases; Neoplasms by Site; Hematologic Diseases; Neoplasms; Hematologic Neoplasms; Graft vs Host Disease
• Other Study ID Numbers: J1484; IRB00039074 (Other Identifier: JHM IRB); P01CA153962 (Other Grant/Funding Number: NIH)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No