Vorinostat Dose-escalation After Allogeneic Hematopoietic Cell Transplantation

Children and adolescents ages 1 to 21 years of age who are undergoing allogeneic
hematopoietic cell transplantation for a myeloid malignancy (AML, MDS, JMML, MPAL) will be
eligible. There are no restrictions on donor type, conditioning, stem cell source, of GVHD
prophylaxis approach.

All participants will be treated on a single arm, and will initially receive 2 cycles of
standard post-transplant azacitidine at a dose of 32mg/m2/dose IV/subcutnaeous for 5 days, in
28 day cycles. This is considered standard of care.

After tolerance of 2 cycles of azacitidine has been established, patients will be assigned to
receive vorinostat orally at different dose levels, depending on the stage of the study. The
dose level assignments will be conducted on a standard 3+3 design, whereby dose-escalation is
peformed if previous patients tolerated the dose without dose-limiting toxicities, and
dose-reduction is performed if dose-limiting toxicities are seen. The starting dose will be
100mg/m2/dose on days 1-7 and 15-21 of each 28 day cycles. This will be in addition to
receiving azacitidine at the fixed dose above. In order to start each cycle, participants
will be required to meet specific clinical parameters to ensure safety.

The dose of vorinostat between patients will be escalated or de-escalated until criteria for
finding the maximum tolerated dose (MTD) is reached, and this will complete the study.
Participants will continue to receive the prescribed dose of vorinostat for up to 7 cycles (9
total cycles of azacitidine).

Participants are followed for dose-limiting toxicities primarily during the first two course
of combined therapy (cycles 3 and 4), but are continued to be tracked until the completion of
all potential combined treatment (1 year or 7 combined cycles, whichever is earlier).

Principal aims:

1. To evaluate the maximum tolerated dose (MTD) of vorinostat used in combination with
low-dose azacitidine after allogeneic hematopoietic cell transplantation (alloHCT) for
childhood myeloid malignancies.

Secondary aims:

1. To describe the dose-limiting toxicities (DLT) of the vorinostat used in combination
with low-dose azacitidine.

2. To describe rates of relapse, transplant related mortality, graft-versus-host disease,
and overall survival.

3. To describe the effect of epigenetic modification on lymphocyte reconstitution in the
post-alloHCT setting.

Inclusion Criteria:

1. Patient is 1 year to 21 years of age.

2. Patient has a diagnosis of AML, MDS, MDS/AML, MPAL, or JMML. Note: patients are
allowed to have received a HMA or HDACi prior to undergoing alloHCT.

3. Patient has undergone allogeneic hematopoietic cell transplantation (no restrictions
on conditioning regimen, donor or stem cell source, or GVHD prophylaxis regimen).

4. Patient and/or parent(s) or legal guardian(s) are capable of understanding the study,
including potential benefits and risks, and sign written informed consent.
Age-appropriate assent will be obtained.

5. Female patient of childbearing potential has a negative screening pregnancy test
(urine or serum, as per local institutional standard).

6. Female patient with infant(s) agrees not to breastfeed her infant(s) while on study.

7. Patient of child-bearing potential (male and female) agrees to use effective method of
contraception during the study.

Exclusion Criteria:

1. Patient is enrolled on a clinical trial with investigational post-transplant
medications. Note: trials involving defibrotide and post-transplant cyclophosphamide
are permitted.

2. Patient has a planned administration of non-protocol chemotherapy, radiation therapy,
donor leukocyte infusion, or immunotherapy during the planned study period.

3. Patient has a known allergy to azacitidine or vorinostat.

4. Patient has chronic myelogenous leukemia.

5. Concomitant use of coumarin-derived anticoagulants or valproic acid.