Total Marrow and Lymphoid Irradiation and Chemotherapy Before Donor Transplant in Treating Patients With Myelodysplastic Syndrome or Acute Leukemia

Inclusion Criteria:

Eligible patients will have a histopathologically confirmed diagnosis of hematologic malignancy in one of the following categories:

Acute myelogenous leukemia

In first complete remission (CR1) with poor risk cytogenetics according to National Comprehensive Cancer Network (NCCN) guidelines for acute myeloid leukemia (AML): monosomal karyotype, -5, 5q-,-7,7q-, inv (3), t(3;3), t(6;9), t(9;22) and complex karyotypes (>= 3 unrelated abnormalities [abn]) and normal cytogenetics with fms-related tyrosine kinase 3 (FLT3)-internal tandem duplications (ITD) mutation
In pediatrics, all of the above and 11q23-non t(9;11)
In second complete remission (CR2) or third complete remission (CR3)
With chemosensitive primary refractory disease

Acute lymphocytic leukemia

In CR1 with poor risk cytogenetics:

For adults according to NCCN guidelines for acute lymphoblastic leukemia (ALL): hypoploidy (< 44 chromosomes); t(v;11q23): mixed lineage leukemia (MLL) rearranged; t(9;22) (q34;q11.2); complex cytogenetics (5 or more chromosomal abnormalities); high white blood cell (WBC) at diagnosis (>= 30,000 for B lineage or >= 50,000 for T lineage)
For pediatrics t(9;22), intrachromosomal amplification of chromosome 21 (iAMP21)loss of 13q, and abnormal 17p
In CR2 or CR3
With chemosensitive primary refractory disease
Myelodysplastic syndrome in high-intermediate (int-2) and high risk categories
Karnofsky or Lansky performance status >= 80
A pretreatment measured creatinine clearance (absolute value) of >= 50 ml/minute
Serum bilirubin =< 2.0 mg/dl
Serum glutamic oxaloacetic transaminase (SGOT) and serum glutamate pyruvate transaminase (SGPT) =< 2.5 times the institutional upper limits of normal
Ejection fraction measured by echocardiogram or multigated acquisition scan (MUGA) >= 50%
Diffusing capacity of the lung for carbon monoxide (DLCO) and forced expiratory volume in one second (FEV1) > 60% predicted
Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control or abstinence) prior to study entry and for six months following duration of study participation; should a woman become pregnant or suspect that she is pregnant while participating on the trial, she should inform her treating physician immediately
The recipient must have a related donor genotypically human leukocyte antigen (HLA)-A, B,C and DRB1 loci haploidentical to the recipient
No HLA matched sibling or matched unrelated donor is available

Patients should be off all previous intensive therapy, chemotherapy or radiotherapy for 3 weeks prior to commencing therapy on this study

* (NOTE: Low dose chemotherapy or maintenance chemotherapy given within 7 days of planned study enrollment is permitted; these include: hydroxyurea, 6-meraptopurine, oral methotrexate, vincristine, oral etoposide, and tyrosine kinase inhibitors [TKIs]; FLT-3 inhibitors such as sorafenib, crenolanib, quizartinib, midostaurin can also be given up to 3 days before conditioning regimen)

Adequate organ function
All subjects must have the ability to understand and the willingness to sign a written informed consent
Prior radiation therapy that would exclude the use of TMLI

DONOR ELIGIBILITY CRITERIA:

DONOR: Age =< 60 years of age
DONOR: For younger donors, no more than 20 mL bone marrow may be harvested per kg of donor body weight
DONOR: Medical history and physical examination confirm good health status as defined by institutional standards
DONOR: Seronegative for human immunodeficiency virus (HIV) antigen (Ag), HIV 1+2 antibody (Ab), human T-lymphotropic virus (HTLV) I/II Ab, hepatitis B surface antigen (HBsAg), hepatitis B core antibody (HBcAb) (immunoglobulin [Ig]M and IgG), hepatitis C virus (HCV) Ab, rapid plasma reagin (RPR) for syphilis within 30 days of apheresis collection
DONOR: Genotypically haploidentical as determined by HLA typing, preferably a non-maternal HLA haploidentical relative; eligible donors include biological parents, siblings or half siblings, or children
DONOR: Female donors of child-bearing potential must have a negative serum or urine beta-human chorionic gonadotropin (HCG) test within three weeks of mobilization
DONOR: The donor must have been informed of the investigational nature of this study and have signed a consent form in accordance with federal guidelines and the guidelines of the participating institution
DONOR: Selection of a haploidentical donor will require absence of pre-existing donor-directed anti-HLA antibodies in the recipient

Exclusion Criteria:

Patients should not have any uncontrolled illness including ongoing or active bacterial, viral or fungal infection

Patients may not be receiving any other investigational agents, or concurrent biological, intensive chemotherapy, or radiation therapy for the previous three weeks from conditioning

* (NOTE: Low dose chemotherapy or maintenance chemotherapy given within 7 days of planned study enrollment is permitted; these include: hydroxyurea, 6-meraptopurine, oral methotrexate, vincristine, oral etoposide, and tyrosine kinase inhibitors [TKIs]; FLT-3 inhibitors such as sorafenib, crenolanib, quizartinib, midostaurin can also be given up to 3 days before conditioning regimen)

History of allergic reactions attributed to compounds of similar chemical or biologic composition to any in the pre- or post-transplant regimen
Pregnant women are excluded from this study
Patients with other active malignancies are ineligible for this study, other than non-melanoma skin cancers
The recipient has a medical problem or neurologic/psychiatric dysfunction which would impair his/her ability to be compliant with the medical regimen and to tolerate transplantation or would prolong hematologic recovery which in the opinion of the principal investigator would place the recipient at unacceptable risk
Patients may not have had a prior autologous or allogeneic transplant
HLA-matched or partially matched (7/8 or 8/8) related or unrelated donor is available to donate
Patients may not have received more than 3 prior regimens, where the regimen intent was to induce remission
Patients treatment history may not include anti-CD33 monoclonal antibody therapy (e.g., SGN-CD33 or Mylotarg)
Subjects, who in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study

DONOR EXCLUSION CRITERIA:

DONOR: Evidence of active infection
DONOR: Medical or physical reason which makes the donor unlikely to tolerate or cooperate with growth factor therapy and leukapheresis
DONOR: Factors which place the donor at increased risk for complications from leukapheresis or granulocyte-colony stimulating factor (G-CSF) therapy
DONOR: HIV positive