Skip to content

HLA-mismatched allogeneic hematopoietic stem cell transplantation for high-risk advanced hematological disease with the adjustments of immunosuppressants and low-dose alemtuzumab.

HLA-mismatched allogeneic hematopoietic stem cell transplantation for high-risk advanced hematological disease with the adjustments of immunosuppressants and low-dose alemtuzumab. - HLA-mismatched HSCT for high-risk hematological disease with adjusted immunosuppressabts and low-dose alemtuzumab

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000018298
Enrollment
28
Registered
2015-07-13
Start date
2015-07-14
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High-risk advanced hematological disease(leukemia and malignant lymphoma in non-remission, MDS with more than 20% of blast, and relapsed disease after allogeneic transplantation)

Interventions

Sponsors

Division of Hematology, Saitama Medical Center, Jichi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients who do not have an available HLA-matched or one locus-mismatched related donor. 2.Patients who have a two- or three-locus-mismatched haploidentical related donor in good condition.(This donor should precede an HLA-matched or one locus-mismatched related donor accoridng to the disease status.) 3.Patients who do not have an HLA-matched or one allele-mismatched unrelated donor, or patients whose disease status preclude time-consuming donor coordination. 4.Patients with high-risk advanced hematological disease. Leukemia and malignant lymphoma in non-remission, MDS with more than 20% of blast, and relapsed disease after allogeneic transplantation are included in high-risk group. 5.Patients who are 16 to 70 years old 6.Patients in performance status of 0 or 1. 7.Patients whose major organ functions are preserved.

Exclusion criteria

Exclusion criteria: 1.Patients with poorly controlled active infection. 2.Patients with coexistence of malignancy. 3.Patients who are pregnant or nursing. 4.Patients with serious mental disorder. 5.Patients with HIV antibody positive. 6.Patients who are allergic to drugs used in conditioning regimen or GVHD prophylaxis.

Design outcomes

Primary

MeasureTime frame
Survival rate at 60 days after transplantation with the engraftment of donor cells and without grade III-IV GVHD

Countries

Japan

Contacts

Public ContactShinichi Kako

Saitama Medical Center, Jichi Medical University Division of Hematology

shinichikako@asahi-net.email.ne.jp0486472111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026