Haploidentical Peripheral Blood Stem Cell Transplantation for Acute Leukemia

Sponsor
Peking University People's Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT03756675
Collaborator
(none)
45
1
84
0.5

Study Details

Study Description

Brief Summary

Allogeneic stem cell transplantation (Allo-HSCT) is the effective and even the only treatment for hematological malignancies. The "GIAC" protocol established by our center has successfully crossed the HLA barrier in HLA-mismatched/haploidentical HSCT. The protocol entails the following: treating donors with granulocyte colony-stimulating factor (G-CSF) to induce donor immune tolerance, intensified immunologic suppression to both promote engraftment and to prevent GVHD, antithymocyte globulin (ATG) was included for the prophylaxis of GVHD and graft rejection, and combination of G-CSF-primed bone marrow harvest (G-BM) and G-CSF-mobilized peripheral blood stem cell harvest (G-PB) as the source of stem cell grafts. But peripheral blood transplantation is still prevalent. Compared with BM, G-PB is more convenient to collect, and the number of T lymphocytes and CD34+ cells is higher. It is reported that G-PB has a higher implantation rate and even a higher disease-free survival rate in sibiling-identical transplantation compared with BM transplantation, whereas there were also reports with different conclusions. This prospective, one-arm clinical cohort study aims to evaluate the safety and efficacy of haplotype peripheral blood stem cell transplantation (PBSCT) in the treatment of acute leukemia.

Condition or Disease Intervention/Treatment Phase
  • Other: haplotype PBSCT

Detailed Description

Allogeneic stem cell transplantation (Allo-HSCT) is the effective and even the only treatment for hematological malignancies. The "GIAC" protocol established by our center has successfully crossed the HLA barrier in HLA-mismatched/haploidentical HSCT. The protocol entails the following: treating donors with granulocyte colony-stimulating factor (G-CSF) to induce donor immune tolerance, intensified immunologic suppression to both promote engraftment and to prevent GVHD, antithymocyte globulin (ATG) was included for the prophylaxis of GVHD and graft rejection, and combination of G-CSF-primed bone marrow harvest (G-BM) and G-CSF-mobilized peripheral blood stem cell harvest (G-PB) as the source of stem cell grafts. But peripheral blood transplantation is still prevalent. Compared with BM, G-PB is more convenient to collect, and the number of T lymphocytes and CD34+ cells is higher. It is reported that G-PB has a higher implantation rate and even a higher disease-free survival rate in sibiling-identical transplantation compared with BM transplantation, whereas there were also reports with different conclusions. This prospective, one-arm clinical cohort study aims to evaluate the safety and efficacy of haplotype peripheral blood stem cell transplantation (PBSCT) in the treatment of acute leukemia.

Study Design

Study Type:
Observational
Anticipated Enrollment :
45 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Haploidentical Peripheral Blood Stem Cell Transplantation for Acute Leukemia
Actual Study Start Date :
Nov 1, 2018
Anticipated Primary Completion Date :
Nov 1, 2023
Anticipated Study Completion Date :
Nov 1, 2025

Arms and Interventions

Arm Intervention/Treatment
haplotype PBSCT group

Subjects in this group will receive haplotype peripheral blood stem cell transplantation (PBSCT) of "GIAC" system in the treatment of acute leukemia.

Other: haplotype PBSCT
haplotype peripheral blood stem cell transplantation (PBSCT) of "GIAC" system

Outcome Measures

Primary Outcome Measures

  1. engraftment rate [one year after transplantation]

    Neutrophil recovery was defined as an absolute neutrophil count(ANC) of 0.5×10^9/L or more for three consecutive days and platelet recovery, as 20×10^9/L or more for seven consecutive days without transfusion.

Secondary Outcome Measures

  1. cumulative incidence of acute graft-versus-host disease(GVHD) [one year after transplantation]

    cumulative incidence of acute graft-versus-host disease(GVHD)

  2. cumulative incidence of chronic GVHD at one year [one year after transplantation]

    cumulative incidence of chronic GVHD at one year

  3. cumulative incidence of relapse at one year [one year after transplantation]

    Cumulative incidence of relapse was defined as the cumulative incidences of presence of morphological evidence of disease in samples from peripheral blood, bone marrow, or extramedullary sites, or by the recurrence and sustained presence of pre-transplantation chromosomal abnormalities.

  4. cumulative incidence of non-relapse mortality (NRM) at one year [one year after transplantation]

    NRM was defined as the death without disease progression or relapse.

  5. overall survival at one year [one year after transplantation]

    OS was defined as the time from the date of first dose until death due to any cause.

Eligibility Criteria

Criteria

Ages Eligible for Study:
2 Years to 60 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • 2-60 years old, all genders;

  • the first complete remission phase (CR1) of acute leukemia;

  • planning to receive haplotype PBSCT;

  • no uncontrolled current infections (new infections, body temperature still above 38 ℃ after treatment with broad-spectrum antibiotics for 72h, except for other non-infectious factors);

  • no organ failure.

Exclusion Criteria:
  • with poor compliance;

  • with uncontrolled current infections;

  • pregnancy;

  • donors with contraindications of mobilization and collection of peripheral blood stem cells;

  • with mental sickness

Contacts and Locations

Locations

Site City State Country Postal Code
1 Peking University People's Hospital Beijing Beijing China 100044

Sponsors and Collaborators

  • Peking University People's Hospital

Investigators

  • Principal Investigator: Xiao-Jun Huang, MD, Peking University People's Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Xiaojun Huang,MD, Supervisor of Hematology, Peking University People's Hospital, Peking University People's Hospital
ClinicalTrials.gov Identifier:
NCT03756675
Other Study ID Numbers:
  • Haplo-PBSCT for AL
First Posted:
Nov 28, 2018
Last Update Posted:
Sep 17, 2020
Last Verified:
Sep 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Xiaojun Huang,MD, Supervisor of Hematology, Peking University People's Hospital, Peking University People's Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 17, 2020