Primary myelofibrosis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.More than Intermediate-2 (DIPSS plus) of primary myelofibrosis 2.HLA-A,-B,-DR antigen fullmatch or 1 locus mismatch related or unrelated donor 3.0 to 2 of ECOG performance status 4.More than 40% of Ejection Fraction in cardiac ultrasonography 5.More than 94% of SpO2 in room air 6.More than 70% of vital capacity and more than 70% of FEV1/FVC 7..Less than 2.0mg/dl of serum bilirubin and less than 5-fold ULN of AST 8.More than 40ml/min of eGFR
Exclusion criteria
Exclusion criteria: 1.Positive of HBs antigen, HCV antibody, HIV antibody or HTLV-1 antibody 2.Uncontrollable psychiatric symptom 3.Pregnant woman or lactating 4.Active other cancers 5.Uncontrollable active infection 6.Hepatic cirrhosis 7.More than BMI 35 8.Others
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Engraftment and survival at 4 weeks after allo-SCT 2.Analysis of cytokine and growth factor during Allo-SCt | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Survival at 12 weeks after allo-SCT 2.Disease status at 4 and 12 weeks after Allo-SCT 3.Acute GVHD 4.Infection 5.Adverse event (CTCAE ver.4 Grade3 or more) 6.Analysis of lymphocyte subsets and immunoglobulin at 4, 8 and 12 weeks after allo-SCT | — |
Countries
Japan
Contacts
Hokkaido University Hospital, Sapporo, Hokkaido, Japan Department of Hematology