Pomalidomide After Combination Chemotherapy in Treating Patients With Newly Diagnosed Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndrome

PRIMARY OBJECTIVES:

I. To define the maximum tolerated dose (MTD) of pomalidomide when given at the time of early
lymphocyte recovery following intensive induction timed sequential therapy (TST) with
cytarabine (cytosine arabinoside), daunorubicin hydrochloride (daunorubicin) and etoposide
(AcDVP-16) in patients with newly diagnosed intermediate- and poor-risk acute myeloid
leukemia and high-risk myelodysplastic syndrome (MDS).

II. To evaluate the safety, tolerability and toxicity of pomalidomide given at the time of
early lymphocyte recovery following induction AcDVP-16 chemotherapy in adults with newly
diagnosed intermediate- and poor-risk acute myeloid leukemia and high-risk MDS.

SECONDARY OBJECTIVES:

I. To evaluate the safety, tolerability and toxicity of pomalidomide given as a continuation
therapy following induction and/or consolidation chemotherapy in adults with newly diagnosed
intermediate- and poor-risk acute myeloid leukemia and high-risk MDS.

II. To document responses (complete remission [CR], CR with incomplete count recovery [CRi],
partial remission [PR]) to AcDVP-16 followed by pomalidomide at the time of lymphocyte
recovery in newly diagnosed adults with intermediate- and poor-risk acute myeloid leukemia
(AML) and high-risk MDS, including duration of response, disease-free and overall survival.

III. Correlative pharmacodynamics studies: a) to characterize the effects of pomalidomide on
the functional dynamics of different lymphocyte subpopulations (effector T [Teff], regulatory
T [Treg], natural killer [NK] cells) and its impact on tumor-associated antigen
(TAA)-specific T cell immunity when given following induction and as a maintenance; b) to
examine for the presence of minimal residual disease (MRD) before and after pomalidomide
administration during induction and continuation therapy; c) to examine cereblon expression
in primary leukemia cells at diagnosis and in sorted T cells prior to and after pomalidomide
treatment.

OUTLINE: This is a dose-escalation study of pomalidomide.

INDUCTION: Patients receive cytarabine intravenously (IV) continuously and daunorubicin
hydrochloride IV on days 1-3 (patients may otherwise receive idarubicin hydrochloride IV over
10-15 minutes on days 1-3 if daunorubicin hydrochloride is unavailable), and etoposide IV
over 3 hours on days 8-10. At the time of early lymphocyte recovery (after day +14), patients
also receive pomalidomide orally (PO) for 10-21 days.

CONSOLIDATION: Patients achieving CR or CRi receive cytarabine based treatment at the
discretion of the treating investigator, with possible regimens comprising cytarabine IV
continuously on days 1-3, and 10-12 and daunorubicin hydrochloride IV on days 1-3, or high-
or medium-dose cytarabine IV every 12 hours on days 1, 3, and 5 for 1-4 courses.

CONTINUATION: Patients achieving CR or CRi who did not undergo allogeneic stem cell
transplant receive pomalidomide PO daily on days 1-21 beginning 6 weeks following blood count
recovery. Treatment repeats every 4-6 weeks for up to 4 courses in the absence of disease
progression or unacceptable toxicity.

After completion of study treatment, patients are followed up for 2 years.

Inclusion Criteria:

- Patients must have histologically or cytologically confirmed:

- Pathologically confirmed intermediate or poor risk newly diagnosed AML (subtypes
M0, 1, 2, 4-7), but excluding newly diagnosed core-binding factor (CBF) (t(8;21)
or M4eo subtype (inv(16) or t(16;16) AMLs and acute promyelocytic leukemia (acute
promyelocytic leukemia [APL], M3)

- MDS with high risk features as defined by intermediate (INT)-2 or high
International Prognostic Scoring System (IPSS) score with > 10% blasts in the
bone marrow

- Chronic myelomonocytic leukemia-2 (CMML-2) defined as having > 10% blasts
(including promonocytes) in the bone marrow or 5-19% blasts (including
promonocytes) in the peripheral blood

- Patients who have received hydroxyurea alone or have received non-cytotoxic therapies
previously for treatment of MDS or myeloproliferative neoplasm (MPN) (e.g.
azacitidine, decitabine, histone deacetylase inhibitors, tyrosine kinase inhibitors,
hematopoietic growth factors, interferon, lenalidomide, thalidomide) will be eligible
for this trial as long as immunomodulatory drugs (e.g. lenalidomide, thalidomide) have
not been used in the past 3 months

- Patients must be off all non-cytotoxic chemotherapies or biologic agents (e.g.
azacitidine, decitabine, histone deacetylase inhibitors, tyrosine kinase inhibitors,
hematopoietic growth factors, interferon, but excluding hydroxyurea and
cyclophosphamide) for at least 2 weeks prior to starting induction chemotherapy

- Patients must be off radiation therapy or chemotherapy 4 weeks (6 weeks for
nitrosoureas or mitomycin C) of starting induction chemotherapy

- All adverse events (excluding alopecia, acne, rash) due to agents administered more
than 2 weeks earlier should recover to =< grade 1; patients with hematologic
malignancies are expected to have hematologic abnormalities at study entry; these
abnormalities which are thought to be primarily related to the underlying leukemia,
are not considered to be toxicities (adverse events [AE]) and do not need to resolve
to =< grade 1

- Patients with therapy-related AML or MDS should have not received prior cumulative
anthracycline (daunorubicin equivalent) lifetime dose > 450 mg/m^2

- Cytoreduction allowed:

- Hydroxyurea, corticosteroids, leukapheresis can be used prior to start of
induction chemotherapy

- Cyclophosphamide up to dose 50-60 mg/kg is allowed for cytoreduction, but must be
given at least 7+/- 2 days before start of induction chemotherapy

- Eastern Cooperative Oncology Group (ECOG) performance status =< 2 (Karnofsky >= 50%)

- Total bilirubin < 2.0 mg/dL unless due to Gilbert's disease, hemolysis or leukemia

- Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase
[SGOT])/alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT])
=< 5 x institutional upper limit of normal unless due to leukemic infiltration

- Creatinine =< 2.0 mg/dL

- Left ventricular ejection fraction >= 45%

- Female who is able to become pregnant must have a negative pregnancy test with a
sensitivity of at least 25 mIU/mL within 10-14 days prior to and again within 24 hours
of starting pomalidomide; female who is able to become pregnant must either commit to
continued abstinence from heterosexual intercourse or begin two acceptable methods of
birth control, one highly effective and one additional effective method at the same
time; female who is able to become pregnant must agree to ongoing pregnancy testing;
men must agree to use a latex condom during sexual contact with female who is able to
become pregnant even if they had vasectomy for the duration of study participation,
and 28 days after completion of pomalidomide administration; all patients must be
counseled at a minimum of every 28 days about pregnancy precautions and risks of fetal
exposure while taking pomalidomide; should a woman become pregnant or suspect she is
pregnant while she or her partner is participating in this study, she should inform
her treating physician immediately

- A female who is able to become pregnant is a sexually mature woman who: 1) has
not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been
naturally postmenopausal for at least 24 consecutive months (i.e., has had menses
at any time in the preceding 24 consecutive months)

- Ability to understand and the willingness to sign a written informed consent document;
consent will be obtained by day 14 of AcDVP-16 induction regimen

- Known human immunodeficiency virus (HIV) infected patients (HIV testing will not be
performed as a part of screening) on combination antiretroviral therapy are eligible
for inclusion; the use of zidovudine is not allowed

Exclusion Criteria:

- Patients who are receiving any other investigational agents or who have received
pomalidomide in the past

- Patients with known active central nervous system leukemia should be excluded from
this clinical trial; patient receiving intrathecal chemotherapy prophylaxis should not
receive pomalidomide for >= 3 days after administration

- History of allergic reactions attributed to compounds of similar chemical or biologic
composition to pomalidomide (e.g. lenalidomide, thalidomide) or other agents used in
study

- The development of erythema nodosum if characterized by a desquamating rash while
taking thalidomide, lenalidomide or similar drugs in the past

- Uncontrolled intercurrent illness including, but not limited to, active and
uncontrolled infection, symptomatic congestive heart failure, unstable angina
pectoris, cardiac arrhythmia, mental deficits, psychiatric illness or history or
social situations that would limit compliance with study requirements; patients with
infection under active treatment and controlled with antibiotics are eligible

- Any other medical condition that in opinion of investigator would place patient at
increased risk for toxicity during pomalidomide treatment (i.e. history of recurrent
or serious thromboembolic events)

- Pregnant women are excluded from this study; breastfeeding should be discontinued if
the mother is treated with pomalidomide

- Known positive patients for infectious hepatitis, type A, B, C

- Active graft-versus-host disease (GVHD) following allogeneic stem cell transplant for
non-AML condition (ex. MDS, MPN, lymphoid malignancy, aplastic anemia) requiring
ongoing use of immunosuppressants