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Mesenchymal Stem Cells in the Treatment of Relapsed/Refractory Severe Acquired Aplastic Anemia

Bone Marrow Mesenchymal Stem Cells in the Treatment of Refractory Severe Acquired Aplastic Anemia

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01297972
Enrollment
9
Registered
2011-02-17
Start date
2011-02-28
Completion date
2013-11-30
Last updated
2014-02-04

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

Conditions

Aplastic Anemia

Keywords

Aplastic Anemia, Mesenchymal Stem Cells

Brief summary

Mesenchymal stem cells have been tested in many autoimmune disorders with encouraging results and may be an alternative to the treatment of immune-mediated severe acquired aplastic anemia.

Detailed description

Acquired aplastic anemia is a bone marrow failure syndrome characterized by and empty bone marrow and low blood counts. Most of the cases are immune-mediated. Allogeneic bone marrow transplant is the preferable treatment modality for patients younger than 40 years with a matched sibling donor. Patients not eligible for transplant are treated with intensive immunosuppressive therapy often based on anti-thymocyte globulin and cyclosporine. However, up to one third of patients treated with immunosuppression are refractory and one third of those who response eventually relapse. Refractory and relapsed cases may be the result of insufficient immunosuppression and these cases may benefit from additional immunosuppression. Mesenchymal stem cells infusion may be a potential treatment option, considering its properties to modulate the immune system. Refractory or relapsed patients with aplastic anemia will be treated with conventional immunosuppressive regimen (anti-thymocyte globulin plus cyclosporine) combined with intravenous infusion of allogeneic unrelated bone marrow mesenchymal stem cells.

Interventions

BIOLOGICALIntravenous bone marrow mesenchymal stem cells infusion

After standard immunosuppressive therapy with rabbit antithymocyte globulin 3,5 mg/Kg/day during 5 days, allogeneic unrelated bone marrow derived mesenchymal stem cells will be infused intravenously. Oral cyclosporine 5 mg/Kg/day (with dose correction weekly to keep serum cyclosporine level between 150-250 mg/dl) up to 6 months will be added.

Sponsors

University of Sao Paulo
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of Acquired Aplastic Anemia * Relapse/refractory to at least 1 immunosuppressive first line treatment * Not eligible to allogeneic bone marrow transplantation

Exclusion criteria

* Previous or current malignancy * Active or latent infectious disease * Positive serologic tests for HIV, HCV, HBV, HTLV-1 and 2, Syphilis or Chagas disease * Previous drug reaction for antithymocyte globulin, cyclosporin or corticosteroids * Severe organic impairment (renal, hepatic, cardiac, pulmonary) * Uncontrolled hypertension or diabetes * Pregnancy * Previous history of allergic reaction to penicillin or streptomycin * Severe psychiatric disorder

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants with Adverse Events as a Measure of Safety and Tolerability of intravenous allogeneic unrelated mesenchymal stem cells infusion in patients with severe acquired aplastic anemia.After the mesenchymal stem cells infusion up to 6 mounth afterAdverse events like allergic reactions,infectious diseases,organ dysfunction or other related to mesenchymal stem cells infusion will be assessed.

Secondary

MeasureTime frameDescription
Level of cytopeniasweekly until 6 months
Transfusional requirementsweekly until 6 monthsUnits of blood or platelets transfused after the mesenchymal stem cells infusion will be measured and compared to previously.
Incidence of infections and febrile neutropeniaweekly until 6 months

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 14, 2026