Patients receiving HLA haploidentical stem cell transplantation with post-transplantation cyclophosphamide
Conditions
Interventions
None listed
Sponsors
Hokkaido University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who receive HLA-haploidentical stem cell transplantation between 2012 and 2015
Exclusion criteria
Exclusion criteria: Not applicable
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| overall survival | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Engraftment 2. The incidence and severity of acute and chronic GVHD 3. Non-relapse mortality 4. The incidence of relapse 5. Disease-free survival 6. Dose and Timing of post-transplantation cyclophosphamide 7. The proportion of patients who need dose reduction or stop of post-transplantation cyclophosphamide 8. Immunosuppressive drugs except for post-transplantation cyclophosphamide 9. The proportion of patients who stopped immunosuppressive drugs within 1 year. 10. The incidence of cardiac toxicity from post-transplantation cyclophosphamide 11. The incidence of hemorrhagic cystitis 12. The incidence of complications associated with haploimmunostorm syndrome 13. The incidence of donor cell-derived hematological malignancies 14. Medical care cost and duration of hospital stay 15. Subgroup analysis according to stem cell source, conditioning regimen, and GVHD prophylaxis 16. Subgroup analysis according to disease risk index (DRI) | — |
Countries
Japan
Contacts
Public ContactJunichi Sugita
Hokkaido University Hospital Department of Hematology
Outcome results
None listed