Overview
Cord blood transplants (CBT) are a standard treatment for adults with blood cancers. MSK has developed a standard ("optimized") practice for cord blood transplant (CBT). This optimized practice includes how patients are evaluated for transplant, the conditioning treatment (standard chemotherapy and total body irradiation therapy) given to prepare the body for transplant, the amount of stem cells transplanted, and how patients are followed during and after transplant.The purpose of this study is to collect information about participant outcomes after CBT following MSK's optimized practice. The researchers will look at outcomes of the CBT treatment such as side effects, disease relapse, GVHD, and immune system recovery after CBT treatment.
Eligibility
Inclusion Criteria:
- I. Acute myelogenous leukemia (AML):
- Complete first remission (CR1) at high risk for relapse such as any of the following:
- Known prior diagnosis of myelodysplasia (MDS) or myeloproliferative disorder (MPD).
- Therapy-related AML.
- Presence of extramedullary leukemia at diagnosis.
- Requirement for 2 or more inductions to achieve CR1.
- Intermediate or high ELN2017 genetic risk AML.
- Any patient unable to tolerate consolidation chemotherapy as would have been deemed appropriate by the treating physician.
- Other high-risk features not defined above.
- Complete second remission (CR2) or greater (CR2+).
- Patients in morphologic remission with persistent cytogenetic, flow cytometric, or molecular aberrations are eligible
II. Acute lymphoblastic leukemia (ALL):
- Complete first remission (CR1) at high risk for relapse such as any of the following:
- Presence of any high-risk cytogenetic abnormalities such as t(9;22), t(1;19), t(4;11) or other MLL rearrangements (11q23) or other high-risk molecular abnormality.
- Failure to achieve MRD- complete remission after induction therapy.
- Persistence or recurrence of minimal residual disease on therapy.
- Any patient unable to tolerate consolidation and/or maintenance chemotherapy as would have been deemed appropriate by the treating physician.
- Other high-risk features not defined above.
- Complete second remission (CR2) or greater (CR2+). Note: ALL with less than 5% blasts
at time of transplant but persistent cytogenetic, flow cytometric or molecular aberrations are eligible.
III. Other acute leukemias: Acute leukemias of ambiguous lineage or mixed phenotype with
less than 5% blasts. Leukemias in morphologic remission with persistent cytogenetic, flow
cytometric or molecular aberrations are eligible.
IV. Myelodysplastic Syndromes (MDS) and Myeloproliferative Disorders (MPD) other than
myelofibrosis:
- International prognostic scoring system (IPSS) risk score of INT-2 or high risk at the
time of diagnosis.
- Any IPSS risk category if life-threatening cytopenia(s) exists.
- Any IPSS risk category with karyotype or genomic changes that indicate high risk for
progression to acute myelogenous leukemia.
- MDS/MPD overlap syndromes without myelofibrosis.
- MDS/ MPD patients must have less than 10% bone marrow myeloblasts and ANC > 0.2
(growth factor supported if necessary) at transplant work-up.
V. Non-Hodgkin lymphoma (NHL) at high-risk of relapse or progression if not in remission:
Eligible patients with aggressive histologies (such as, but not limited to, diffuse large
B-cell NHL, mantle cell NHL, and T-cell histologies) in CR by PET/CT imaging.
o Eligible patients with indolent B-cell NHL (such as, but not limited to, follicular,
small cell or marginal zone NHL) will have 2 nd or subsequent progression with PR or CR by
PET/CT imaging.
VI. Blastic plasmacytoid dendritic cell neoplasm (BPDCN) in morphologic remission.
Prior treatment:
To prevent graft rejection, patients who received only non-lymphodepleting agents for their
malignancy (hypomethylating agents, venetoclax, hydroxyurea, TKIs etc.), or patients who
received lymphodepleting chemotherapy > 3 months prior to scheduled admission, should
receive fludarabine 25 mg/m2 daily x 3 days for lymphodepletion 14-42 days (aiming for 2-4
weeks) prior to admission in order to qualify for the protocol.
Organ Function and Performance Status Criteria:
- Karnofsky score equal or greater than 80% (See Appendix B; inpatient Leukemia service
transfers without discharge are acceptable provided patient has equivalent KPS as if
were outpatient).
- Calculated creatinine clearance > 70 ml/min.
- Bilirubin < 1.5 mg/dL (unless benign congenital hyperbilirubinemia or hemolysis).
- ALT < 3 x upper limit of normal (ULN).
- Pulmonary function: Spirometry (FVC and FEV1) and corrected DLCO) > 60% predicted.
- Left ventricular ejection fraction (MOD-bp)> 50%.
- Albumin > 3.0.
- Hematopoietic Cell Transplantation Comorbidity index (HCT-CI) ≤5.
Graft criteria:
Two CB units will be selected according to current MSKCC CB unit selection algorithm. High
resolution 8-allele HLA typing and recipient HLA antibody profile will be performed. Unit
selection will occur based on HLA-match, total nucleated cell (TNC) and CD34+ cell dose
adjusted per patient body weight. The bank of origin will also be considered. Donor
specific HLA antibodies, if present, will also be taken into consideration and may
influence the selection of the graft.
- Each CB unit must be at least 3/8 HLA-matched to the patient considering
high-resolution 8-allele HLA typing. [Taken from the Cord Blood Summary]
- Each CB unit will be required to have a cryopreserved TNC dose of at least 1.5 x 10^7
TNC/ recipient body weight (TNC/ kg). [Taken from the Cord Blood Summary]
- Each CB unit will be required to have a cryopreserved CD34+ cell dose of at least 1.5
x 10^5 CD34+ cells/ recipient body weight (CD34+ cells/kg). [Taken from the Cord Blood
Summary]
- A minimum of one unit will be reserved as a backup graft. [Taken from the Cord Blood
Summary]
- Each CB unit will be required to be cryopreserved in standard cryovolume (24-27 ml/s
per unit or per bag if unit in two bags) and be red blood cell depleted. [Taken from
the Cord Blood Summary]
Exclusion Criteria:
- Diagnosis of myelofibrosis or other malignancy with moderate-severe bone marrow
fibrosis.
- Patients persistent with CNS involvement in CSF or CNS imaging at time of screening
- Prior checkpoint inhibitors/ blockade in the last 12 months.
- Two prior stem cell transplants of any kind.
- One prior autologous stem cell transplant within the preceding 12 months.
- Prior allogeneic transplantation.
- Prior involved field radiation therapy that would preclude safe delivery of 400cGy TBI
in the opinion of Radiation Oncology.
- Active and uncontrolled infection at time of transplantation.
- HIV infection.
- Seropositivity for HTLV-1.
- Inadequate performance status/ organ function.
- Pregnancy or breast feeding.
- Patient or guardian unable to give informed consent or unable to comply with the
treatment protocol including appropriate supportive care, long-term follow-up, and
research tests.