ONC 201 Maintenance Therapy in Acute Myeloid Leukemia and Myelodysplastic Syndrome After Stem Cell Transplant

  • STATUS
    Recruiting
  • End date
    Jul 25, 2024
  • participants needed
    20
  • sponsor
    Vijaya Bhatt
Updated on 4 October 2022
remission
myeloid leukemia
granulocyte colony stimulating factor
growth factor
leukemia
bone marrow procedure
minimal residual disease
residual tumor
blast cells
aml/mds
colony stimulating factor
TP53
blood transfusion

Summary

This is a single-center pilot study of 20 patients with AML/MDS. Eligible patients will be enrolled following an informed consent between 6-20 weeks after allogeneic hematopoietic stem cell transplant. Patients will receive weekly oral ONC 201 for a total of 52 weeks.

Description

This is a single-center pilot study of 20 patients with AML/MDS. Eligible patients will be enrolled following an informed consent between 6-20 weeks after allogeneic hematopoietic stem cell transplant. Patients will receive weekly oral ONC 201 for a total of 52 weeks.

The objectives of the study are: 1. To determine the safety and preliminary efficacy of ONC 201 maintenance therapy among patients with acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS), who undergo allogeneic hematopoietic stem cell transplant. 2. To investigate the impact of ONC 201 on reconstitution of NK and other immune cells.

Patients will be monitored for toxicities (using Common Terminology Criteria for Adverse Events, CTCAE version 5.0), quality of life (Functional Assessment of Cancer Therapy-Bone Marrow Transplant, FACT-BMT), and immunologic changes. We will specifically investigate the impact of ONC 201 on reconstitution of NK and other immune cells. We will also examine changes in functional status (Karnofsky Performance Scale, KPS, instrumental activities of daily living and short physical performance battery), rates of disease relapse and mortality.

Details
Condition Acute Myeloid Leukemia, Myelodysplastic Syndromes
Treatment ONC201
Clinical Study IdentifierNCT03932643
SponsorVijaya Bhatt
Last Modified on4 October 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

A history of AML or MDS with at least one of the following features
AML: High-risk AML as defined by the 2017 European LeukemiaNet criteria (e.g
complex karyotype with ≥3 changes), AML with high-risk mutations (e.g. TP53
RUNX1, or ASXL1 mutations), transplant being performed in second remission or
beyond, or AML with active disease or minimal residual disease positivity
before or after transplant
MDS: MDS with high or very-high risk cytogenetic changes as used indefined by
the Revised International Prognostic Scoring System (e.g. complex karyotype
with ≥3 changes),53 the presence of TP53 mutation, high-risk or very high-risk
MDS not responding to 4 cycles of hypomethylating agents, MDS progressing
following initial response, persistence of MDS after transplant, or transplant
being performed in second remission or beyond
Receipt of allogeneic hematopoietic stem cell transplant 6-20 weeks prior to enrollment
Disease status: <5% bone marrow blast at the time of enrollment
All donor sources and conditioning regimens are allowed
Adults, Age ≥19 years (for the state of Nebraska)
Karnofsky Performance Status (KPS) of ≥70
Absolute neutrophil count (ANC) greater than 1000/µL without the use of granulocyte colony stimulating factor in the past 2 weeks, and platelet count 50,000/µL without platelet transfusion in the past 2 weeks
Able to take oral medication
Female patient of reproductive potential must have a negative serum or urine pregnancy test ≤7 days prior to starting the study drug
Male and female patients of reproductive potential must be willing to avoid pregnancy or fathering children from enrollment to two months after the end of study treatment. This will require either a total abstinence, OR exclusively non-heterosexual activity (when this is in line with the preferred and usual lifestyle of the subject), OR two methods of contraception
Written informed consent to participate in the study

Exclusion Criteria

Use of prednisone at a dose of ≥0.25 mg/kg/day (or equivalent dose of another glucocorticoid) at the time of enrollment
Total bilirubin, aspartate transaminase, alanine transaminase 2 X the upper limit of the normal range. Patients with elevated bilirubin secondary to Gilbert syndrome will not be excluded
A history of acute graft-versus-host disease grade III/IV or initiation of any new immunosuppressive agent for treatment of graft-versus-host disease within 4 weeks prior to enrollment. Oral beclomethasone or budesonide, empirically used for possible but not biopsy-proven graft-versus-host disease, will not be considered an exclusion criterion
Active uncontrolled bacterial, fungal, parasitic, or viral infection. Infections are considered controlled if appropriate therapy has been instituted and, at the time of screening, no signs of infection progression are present. Progression of infection is defined as hemodynamic instability attributable to sepsis, new symptoms, worsening physical signs or radiographic findings attributable to infection. Persisting fever without other signs or symptoms will not be interpreted as progressing infection
Presence of known HIV infection, active hepatitis B or C infection
Creatinine clearance <30 mL/min
Presence of uncontrolled cardiopulmonary conditions such as ongoing cardiac arrhythmias, unstable angina or myocardial infarction, New York Heart Association class III/IV congestive heart failure, or severe chronic obstructive pulmonary disease or other pulmonary condition resulting in a requirement of supplemental oxygen or having a resting O2 saturation <90% by pulse oximetry
Pregnancy or breastfeeding
Known hypersensitivity, or intolerance to any of the study medications, or excipients
Treatment with any other investigational agent, device, or procedure, within 21 days (or 5 half-lives, whichever is greater)
Patients on dopamine antagonists for treatment of psychotic disorder or Parkinson's disease will be excluded. A brief use of drugs such as clozapine or haloperidol for a few days for treatment of nausea or other indication will not be prohibited. The use of tricyclic antidepressants does not constitute an exclusion criterion
Any other condition that is judged by the physician to potentially interfere with compliance to the study protocol or pose a significant risk to the patient
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