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Interferon-γ (IFN-γ) With Donor Leukocyte Infusion to Treat Relapsed Acute Myeloid Leukemia and Myelodysplastic Syndromes Post Allogeneic Hematopoietic Stem Cell Transplantation

S

Sawa Ito, MD

Status and phase

Enrolling
Phase 2

Conditions

Myelodysplastic Syndromes
Acute Myeloid Leukemia

Treatments

Biological: Donor Leukocyte Infusion (DLI)
Drug: Interferon gamma-1b

Study type

Interventional

Funder types

Other
Other U.S. Federal agency
Industry

Identifiers

NCT06529731
1R01FD008187-01 (U.S. FDA Grant/Contract)
HCC 23-160

Details and patient eligibility

About

This phase 2 study aims to confirm the efficacy observed in the prior phase 1 trial in Cohort 1 and to evaluate the safety of IFN-γ in combination with DLI in Cohort 2, the haploidentical donor alloSCT recipient cohort. The study will further contribute to this effort through the collection of leukemia cells pre- and post-in vivo IFN-γ therapy. As in the previously conducted phase 1 trial, this trial will assess whether leukemia blasts are responsive to IFN-γ in vitro and in vivo. Single-cell RNA sequencing (scRNAseq) will be performed to evaluate transcriptomic changes induced by IFN-γ in leukemia cell subsets, including those with stem cell characteristics.

Full description

This novel regimen has the potential to address a significant unmet need for this high-risk population of patients who have few, if any, effective therapeutic options. In Cohort 1, if this trial confirms the clinical efficacy of IFN-γ/DLI in patients with relapsed AML/MDS after HLA-matched alloSCT, it may establish a new therapeutic approach for post-transplant AML/MDS relapse. Cohort 2 will further evaluate the safety and potential efficacy of IFN-γ/DLI in patients with relapsed AML/MDS after haploidentical alloSCT, where treatment options are also limited and the risk of GVHD requires careful assessment. Together, these cohorts would provide a rationale to explore additional indications for IFN-γ in the context of alloSCT, including 1) IFN-γ/DLI for relapsed disease after haploidentical alloSCT; 2) pre-emptive post-alloSCT treatment of patients transplanted with measurable residual disease (MRD) or with poor-risk AML/MDS, such as disease with TP53 mutations; and 3) prevention of relapse in patients who can only tolerate reduced-intensity conditioning regimens, which in most studies are associated with higher rates of post-alloSCT AML/MDS relapse than intensive conditioning regimens. Collectively, this work may allow more patients with AML/MDS to be referred for and ultimately benefit from alloSCT.

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Enrollment

57 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age ≥ 18 years

  2. Recipients of an alloSCT for AML or MDS from a minimally 8/8 HLA-matched donor (Cohort 1: HLA -matched alloSCT recipients) or recipients of a haploidentical donor SCT for AML or MDS from a minimally 4/8 HLA-matched donor (Cohort 2: Haplo-SCT recipients)

  3. AML/MDS relapsed post-alloSCT with measurable residual disease defined by either of the following criteria:

    1. At least 5% or more myeloblasts based on bone marrow biopsy morphology by pathologist review. Abnormal myeloblasts cannot not exceed 30% overall 36
    2. At least 0.1% of abnormal myeloblasts with a leukemia-associated immunophenotype (LAIP) by multiparameter flow cytometry. The abnormal cells with LAIP should not exceed 30% of nucleated cells.
    3. Recurrent or persistent cytogenetic abnormalities detectable by FISH or karyotype analysis.
    4. For patients with mutant NPM1, at least 1,000 mutant transcript copies per 106 ABL or equivalent housekeeping transcripts in bone marrow by qPCR or dPCR

  4. Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) 0-2

  5. A DLI is available, or the donor is available and agrees to undergo apheresis to collect lymphocytes for infusion

  6. If salvage therapy for post-alloSCT relapse was received, the therapy is limited to 1 line of the following:

    1. For hypomethylating agents, venetoclax, and targeted therapies (e.g., tyrosine kinase inhibitors, IDH1/IDH2 inhibitors, or FLT3 inhibitors), the last dose must be > 2 week prior to the initiation of IFN-γ
    2. For cytotoxic chemotherapy agents, the last dose must be >2 weeks prior to start of treatment for the present study
    3. For investigational agents, the last dose must be ≥ 4 weeks or 5 half-lives (whichever is longer) prior to the start of treatment for the present study

  7. Provision of signed and dated informed consent form

  8. Stated willingness to comply with all study procedures and availability for the duration of the study

  9. For female subject, who is < 55 years old without hysterectomy, oophorectomy or documented menopause, willingness to use two forms of contraception including one form of highly effective contraception (i.e., long-acting reversible contraception, oral contraceptive pills) for the duration of the study

  10. For male subject, willingness to use highly effective contraception methods including male condoms by male subject and one form of highly effective contraception by his female partner (i.e., long-acting reversible contraception, oral contraceptive pills) for the duration of the study

Exclusion criteria

  1. Primary engraftment failure after alloSCT
  2. Evidence of mixed phenotype leukemia with lymphoid differentiation (Cohort 1: HLA -matched alloSCT recipients)
  3. Grade 3 or 4 aGVHD per Mount Sinai Acute GVHD International Consortium (MAGIC) at the time of planned enrollment
  4. History of grade 4 aGVHD per the MAGIC criteria
  5. Moderate or severe cGVHD per NIH Consensus Criteria at time of planned enrollment
  6. Any systemic immunosuppressive medications taken within 2 weeks before the enrollment
  7. Grade 3 or higher non-hematologic toxicity related to any prior therapy at the time of enrollment
  8. A contraindication to receive IFN-γ including a known hypersensitivity to IFN-γ, E. coli derived products or any other component of the product
  9. Positive pregnancy test or currently breastfeeding on Day 1 of study treatment 37
  10. Active cardiac arrhythmia not controlled by medical management or current NYHA class II or higher congestive heart failure within 2 months of enrollment unless it was due to a tachyarrhythmia which is under control at the time of enrollment
  11. Active ischemic heart disease not controlled with medications within 2 months of enrollment
  12. Acute or chronic pulmonary disease requiring continuous oxygen treatment
  13. Seizure disorder not controlled by medications within 2 months of enrollment
  14. AST or ALT > 5x ULN or total bilirubin >3x ULN at time of enrollment
  15. Renal function CrCl <30 mL/min at time of enrollment using modified Cockcroft-Gault formula
  16. Detection of HLA loss of heterozygosity (LOH) in relapsed malignant cells. Specifically, there has been a loss of the mismatched set of HLA alleles encoded on chromosome 6 (ie uniparental disomy of chromosome 6), within 30 days prior to enrollment (Cohort 2: Haplo-SCT recipients)

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

57 participants in 2 patient groups

Cohort 1: IFN-γ + DLI (HLA-matched donor alloSCT recipient cohort)
Experimental group
Description:
ACTIMMUNE® (IFN-γ-1b) at a dose of 50 mcg/m\^2 (All participants will receive a 4-week period of IFN-γ monotherapy with ACTIMMUNE 100 mcg 3 times a week. This dose and schedule will be continued for 4 additional weeks and then tapered to 100 mcg weekly for an additional 4 weeks) DLI at a dose of 10\^7 CD3+ cells/kg (DLI doses will be given pending clinical assessment for disease, graft versus host disease (GVHD) and peripheral blood donor chimerism the week prior to DLI. Second DLI dose is only offered to subjects with residual disease not requiring cytotoxic therapy and without GVHD)
Treatment:
Drug: Interferon gamma-1b
Biological: Donor Leukocyte Infusion (DLI)
Cohort 2: IFN-γ + DLI (Haploidentical donor alloSCT recipient cohort)
Experimental group
Description:
ACTIMMUNE® (IFN-γ-1b) at a dose of 50 mcg/m\^2 (All participants will receive a 4-week period of IFN-γ monotherapy with ACTIMMUNE 100 mcg 3 times a week. This dose and schedule will be continued for 4 additional weeks and then tapered to 100 mcg weekly for an additional 4 weeks) DLI at a 1st dose of 10\^6 CD3+ cells/kg, 2nd dose at a dose of 10\^7 CD3+ cells/kg (DLI doses will be given pending clinical assessment for disease, graft versus host disease (GVHD) and peripheral blood donor chimerism the week prior to DLI. Second DLI dose is only offered to subjects with residual disease not requiring cytotoxic therapy and without GVHD)
Treatment:
Drug: Interferon gamma-1b
Biological: Donor Leukocyte Infusion (DLI)

Trial contacts and locations

3

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Central trial contact

Amy Rodger, RN; Linda Elias, RN

Data sourced from clinicaltrials.gov

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