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Phase 2 N=36 Treatment

Peginterferon Alfa-2a to Enhance Anti-leukemic Responses After Allogeneic Transplantation in Acute Myeloid Leukemia

Acute Myeloid Leukemia

Enrolled (actual)
36
Serious AEs
27.8%
Results posted
Oct 2021
Primary outcome: Primary: Phase 1: Maximum Tolerated Dose (MTD) of Peg-IFN-α — 180 mcg

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
peg-IFN-α (Drug); Hematopoietic Cell Transplant (HCT) (Procedure); Tacrolimus (Drug); Methotrexate (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Michigan Rogel Cancer Center
Primary completion
Mar 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Phase 1: Maximum Tolerated Dose (MTD) of Peg-IFN-α
180
PRIMARY
Phase 2: Number of Patients That Relapse
39; 67; 39
SECONDARY
Phase 2: Overall Survival Time
55; 33; 55; 33
SECONDARY
Phase 2: Event Free Survival Time
48; 28
SECONDARY
Acute GVHD
39
SECONDARY
Non-Relapse Mortality
13; 25

Summary

This protocol is an open label, single arm, non-randomized, phase I / II clinical trial investigating the use of pegylated interferon alpha-2a (peg-IFN-α, Pegasys®, Genentech) for prevention of relapse in acute myeloid leukemia (AML) not in remission at the time of allogeneic hematopoietic stem cell transplantation (HCT).

Eligibility Criteria

Inclusion Criteria

  • Patient must have AML not in remission or at very high risk for HCT (Hematopoietic Cell Transplantation) relapse.
  • For newly diagnosed AML, patients must have achieved two consecutive induction attempts without achieving complete remission
  • For patients initially in complete remission whose AML relapses > 6 months after preceding remission, one re-induction must be attempted to be eligible
  • For AML patients with early relapse, in whom the preceding remission is shorter than 6 months duration, no re-induction regimen is necessary to be eligible
  • Patients with antecedent MDS (Myelodysplastic Syndrome) who progress to AML may have therapies rendered during both phases counted towards these requirements.
  • Patients with poor cytogenetic or molecular risk associated with very high risk for relapse after HCT may proceed without provisions for prior treatment. However, they must have received at least one induction attempt.
  • Patients must be ≥ 18 years of age and considered a candidate for HCT
  • Karnofsky ≥ 70% (Karnofsky performance status is measure of a cancer patients general well being and activities of daily life. Scores range from 100 to 0 where 100 is perfect health and 0 is death
  • Patients must meet acceptable organ function criteria: Total Bilirubin ≤2.5 mg%; AST (Aspartate transaminase) and ALT (Alanine transaminase) 40 mL/min/1.73 m2 for patients with creatinine levels above institutional normal; Lung function tests (DLCO, FEV1, FVC) > 50%; Ejection fraction > 50%
  • All patients must sign an informed consent
  • Women and men of child-bearing potential must agree to use adequate contraception

Exclusion Criteria

  • Prior chemotherapy treatment for AML within 21 days from the initiation of HCT conditioning
  • Patients may NOT have evidence or symptoms of CNS disease at the time of enrollment
  • HIV or HTLV1 / HTLV2 (Human T-lymphotrophic virus) (seropositivity and/or PCR positivity)
  • Patients less than 18 years of age
  • Pregnant and nursing mothers are excluded from this study
  • Patients with untreated or uncontrolled neuropsychiatric illness
  • Any physical or psychological condition that, in the opinion of the investigator, would pose unacceptable risk to the patient
  • Uncontrolled infections
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02328755). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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