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Effect of autologous hemapoietic stem cell transplantation combined with the infusion of haploidentical granulocyte-colony stimulating factor mobilized peripheral blood mononuclear cells in the treatmen of patients with hematologic malignancies: a multicenter, prospectively randomized controlled study

Autologous hemapoietic stem cell transplantation combined with the infusion of haploidentical granulocyte-colony stimulating factor mobilized peripheral blood mononuclear cells improves the outcome of patients with hematologic malignancies

Status
Unknown
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IIR-16008212
Enrollment
Unknown
Registered
2016-04-03
Start date
2016-04-05
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

hematologic malignancies

Interventions

Experimental group:Autologous hemapoietic stem cell transplantation combined with the infusion of haploidentical granulocyte-colony stimulating factor mobilized peripheral blood stem cells
Control group:Autologous hemapoietic stem cell transplantation

Sponsors

Department of Hematology, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients with hematologic malignancies with medium-high risk who achieved over PR after three cycle chemotherapy; 2. Male or Female; Aged <60 years; 3. KPS is over 60 and survival is over three months; 4. No serious systemic organ dysfunction and ECOG performance status of <=2 at study entry; 5. Understand and voluntarily sign an informed consent.

Exclusion criteria

Exclusion criteria: 1. Serious systemic organ dysfunction; 2. Patient with malignant tumor that needs to be treat; 3. The patients with clinical symptom of brain dysfunction or serious psychiosis that can't understand or obey the study; 4. Patients that can't followed up as scheduled; 5. Patients that can't guarantee complete the plan and follow up.

Design outcomes

Primary

MeasureTime frame
overall survival;

Secondary

MeasureTime frame
disease-Free survival;Rate of relapse;Time of hematopoietic recovery;Rate of GVHD;Donor chimerism;

Countries

China

Contacts

Public ContactCheng Zhang

Department of Hematology, Xinqiao Hospital, Third Military Medical University

1764180534@qq.com+86 23 68774209

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026