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Completed

NCT Number: NCT02331706

IFN-DLI for Relapsed Acute Leukemia After Allo-SCT

This trial is designed to determine the feasibility of conventional induction chemotherapy, IFNand G-CSF mobilized DLI (IFN-DLI) in subjects with relapsed AML and ALL after allo-SCT.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Abramson Cancer Center of the University of Pennsylvania

Philadelphia, Pennsylvania, 19104, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

DLI Recipient

  • Relapsed AML or ALL ≥ 60 days after allogeneic SCT.
  • Evidence of residual donor chimerism on most recent analysis (within 4 weeks of enrollment).
  • Age ≥ 18 years of age,
  • Karnofsky performance status ≥ 60%.
  • Absence of active GVHD and off immunosuppression. Subjects on tapering prednisone will be eligible if their dose is 0.25 mg/kg or less and being actively tapered. We suggest a 28 day waiting period off of immunosuppression but some subjects with rapidly progressive disease may need to be treated before 30 days and will still be eligible.
  • Adequate organ function: Cr ≤ 2 mg/dL; ALT/AST < 3x ULN, direct bili <3x ULN.
  • Matched sibling or un-related donor (A, B, C, and DR) available to undergo leukopheresis.
  • Subjects must be able to sign consent and be willing and able to comply with scheduled visits, treatment plan and laboratory testing.
  • Willing to provide blood samples for research purposes.
  • Willing to adhere to medically accepted form of birth control to prevent pregnancy (includes: complete abstention from intercourse, condoms, diaphragms, cervical cap, intra-uterine device, history of surgical sterility - tubal ligation or vasectomy in patient or partner, or oral contraceptive).

DLI Donor

  • HLA identical to recipient subject.
  • Considered medically eligible for leukopheresis procedure by independent donor physician (University of Pennsylvania physician who is not the recipient's primary transplant physician for related donors; physician designated by National Marrow Donor Program for unrelated donors).
  • Considered medically eligible to receive G-CSF (filgrastim) by independent donor physician.

Exclusion criteria

Recipient

  • Prior cell therapy for relapse within the past 90 days.
  • Requirement for active immunosuppression to treat GVHD.
  • Pregnant or lactating women. The safety of this therapy on unborn children and effects on breast milk are not known.
  • Uncontrolled active infection
  • Any uncontrolled active medical disorder that would preclude participation as outlined.

Donor

  • Unable to participate in a leukopheresis procedure or receive G-CSF (filgrastim).

Treatment and study plan

Interferon alpha-2B (IFN-α) 3 million units (MU) subcutaneous daily

Drug

Primary outcomes

  1. Number of Adverse Events

    Time frame: 2 years

Secondary outcomes

  1. overall survival

    Time frame: 2 years

  2. disease-free survival

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Abramson Cancer Center at Penn Medicine

Other

Registry information

Official study title

A Pilot Study to Determine the Feasibility of Conventional Induction Chemotherapy Followed by G-CSF Mobilized Donor Leukocyte Infusion (DLI) and IFN-α (IFN-DLI) for Relapsed Acute Leukemia After Allogeneic Stem Cell Transplantation.

Important dates

Study start
2014
Primary completion
2016
Study completion
2017
First posted
Jan 6, 2015
Registry last updated
Apr 21, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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