IMRT-TMI With Fludarabine as Myeloablative Conditioning for Allogeneic HSCT

This is a phase I/II clinical trial to determine the maximum tolerated dose (MTD) of
intensity modulated radiation therapy based total marrow irradiation (TMI) in combination
with fludarabine in the context of a myeloablative conditioning regimen for allogeneic
hematopoietic stem cell transplantation (Allo-HSCT), as well as to determine the efficacy of
the regimen in patients with high-risk and relapsed or refractory leukemia and
myelodysplasia. TMI, which allows for conformal dosing of target bone marrow tissue while
giving lower doses to organs at risk, is considered by many to be a superior alternative to
conventional total body irradiation (TBI)

Primary Objectives:

Phase I component:

Determine the MTD of TMI given concurrently with fludarabine (fixed at 150 mg/m2) as a
conditioning regimen for Allo-HSCT for patients with high risk (relapsed/refractory) acute
lymphocytic leukemia (ALL), acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), and
chronic myelogenous leukemia (CML).

Phase II component:

Single-arm exploratory study to expand the cohort at the MTD level to estimate 1- year
overall survival (OS), with the objective of increasing the OS from the historical rate of
30% (null hypothesis ) to 50% (alternate hypothesis) with 80% power and a one-sided type I
error of 0.05.

Secondary Objectives

1. Describe the extramedullary toxicity and the incidence of complications, including
mucositis, acute and chronic graft versus host disease (GvHD), sinusoidal obstruction
syndrome (SOS), and pneumonitis.

2. Describe the time to engraftment of neutrophils and platelets

3. Describe the disease response rate at day 30 after transplantation

4. Describe the overall survival and disease-free survival

5. Describe the cumulative incidence of relapse and non-relapse mortality

6. Determine the correlation between plasma/serum markers and radiation induced acute and
long term toxicities.

Inclusion Criteria:

1. Patients must be diagnosed with one of the following conditions:

Acute Myeloid Leukemia (AML) who are not in complete remission, and who have either
primary refractory or relapsed disease, and who do not have more than one of the
following adverse factors:

1. Duration of first CR < 6 months (if previously in CR)

2. Poor risk karyotype including any of the following: complex karyotype with ≥3
clonal abnormalities, 5q-/-5, 7q-/-7, 11q23 abnormalities, inv(3q), 20q or 21q
abnormalities, t(6;9), t(9;22), 17p abnormalities [or TP53 mutations] or
monosomal karyotype. Molecular typing (except for TP53 mutation) will not be used
for eligibility criteria determination.

3. Circulating peripheral blood blasts at time of enrollment

4. Karnofsky performance status <90%

Acute Lymphocytic Leukemia (ALL) who are not in complete remission, and who have
either primary refractory or relapsed disease, and who do not have more than one of
the following adverse factors:

1. First refractory relapse. Patients in second or subsequent relapse are excluded.

2. Donor is CMV seropositive

3. Bone marrow blasts >25% (within 30 days of admission)

4. Age >40 years

Myelodysplasia with a Revised International Prognostic Score (IPSS-R) of greater than
4.5 (i.e., high- or very-high risk).

Chronic Myelogenous Leukemia (CML) in either

1. Accelerated phase, defined by any of the following:

- Blasts 10-19% in peripheral blood white cells or bone marrow

- Peripheral blood basophils at least 20%

- Persistent thrombocytopenia (<100 x 109/l) unrelated to therapy, or
persistent thrombocytosis (>1000 x 109/l) unresponsive to therapy

- Increasing spleen size and increasing white blood cell (WBC) count
unresponsive to therapy

- Cytogenetic evidence of clonal evolution (i.e., the appearance of an
additional genetic abnormality that was not present in the initial specimen
at the time of diagnosis of chronic phase)

2. Chronic phase provided a complete hematologic remission was not achieved by 3
months or a complete cytogenetic remission by 18 months and the patient had
received at least 2 tyrosine kinase inhibitors.

2. Patient age 18-65 years

3. Availability of a consenting human leukocyte antigens(HLA) -matched donor

4. Karnofsky Performance Status 70% or higher

5. Required baseline laboratory values:

1. Estimated creatinine clearance ≥ 60 ml/min

2. Aspartate aminotransferase and alanine aminotransferease ≤ 2.5 x upper limit of
normal value

3. Bilirubin ≤ 1.5 x upper limit of normal value

6. Required baseline cardiac function of left ventricular ejection fraction (LVEF) > 45 %
corrected

7. Required baseline pulmonary function of lung diffusing capacity (DLCO) > 45 %
predicted (corrected for hemoglobin)

8. Patient must be capable of understanding the investigational nature of this study,
potential risks and benefits of the study, and be able to provide a valid informed
consent.

Exclusion Criteria:

1. Patients with ALL who are in second or subsequent relapse

2. Active infection: Patients with active infections requiring oral or intravenous
antimicrobial drugs are not eligible for enrollment until resolution of infection.

3. HIV seropositive patients.

4. Pregnant or nursing females are excluded from this study.

5. Prior radiation therapy

6. Patients who have had a prior autologous or allogeneic bone marrow or stem cell
transplantation