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Study of Fludarabine + Cyclophosphamide + TBI Conditioning Regimen for Double Units Cord Blood Transplantation(CBT)in Severe Aplastic Anemia(SAA)

Phase I/II Study of Fludarabine, Cyclophosphamide Plus TBI Conditioning Regimen for Double Units Cord Blood Transplantation in Severe Aplastic Anemia

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00881933
Enrollment
5
Registered
2009-04-15
Start date
2008-11-30
Completion date
2012-09-30
Last updated
2012-03-26

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

Conditions

Aplastic Anemia

Keywords

Fludarabine, Cyclophosphamide, TBI, severe aplastic anemia,, cord blood transplantation, pediatric

Brief summary

Severe aplastic anemia is a fatal disease and patients without HLA matched siblings need alternative treatment option. Cord blood transplantation (CBT) has become an alternative treatment means in various diseases, but it has not been proved to be good for severe aplastic anemia. Double units CBT is proposed to have better engraftment potential and and we reported successful double units UCBT after engraftment failure with single unit with promising result. To increase the engraftment potential, fludarabine, cyclophosphamide plus TBI conditioning regimen for double units cord blood transplantation was proposed for the patient with severe aplastic anemia without HLA-matched donor.

Interventions

OTHERCyclophosphosphamide, TBI

fludarabine (30 mg/m2 once daily i.v. on days -7, -6, -5, -4, -3, & -2) (if body weight \< 10 kg or if age \< 1 year: 1.33 mg/kg) cyclophosphamide (60 mg/kg once daily i.v. on days -9, & -8) total body irradiation (3G on days -1)

Sponsors

The Korean Society of Pediatric Hematology Oncology
Lead SponsorNETWORK

Study design

Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Years to 21 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of severe aplastic anemia defined by any two or three peripheral blood criteria and either marrow criterion. * Peripheral blood * Neutrophils \< 0.5 x 109/l * Platelets \< 20 x 109/l * Corrected reticulocytes \< 1% * Bone marrow * Severe hypocellularity (\< 25%) * Moderate hypocellularity (25-30%) with hematopoietic cells representing \< 30% of residual cells * No prior hematopoietic stem cell transplantation. * Age: no limits. * Performance status: ECOG 0-2. * Patients must be free of significant functional deficits in major organs, but the following eligibility criteria may be modified in individual cases. * Heart: a shortening fraction \> 30%, ejection fraction \> 45%. * Liver: total bilirubin \< 2 × upper limit of normal; ALT \< 3 × upper limit of normal. * Kidney: creatinine \<2 × normal or a creatinine clearance (GFR) \> 60 ml/min/1.73m2. * Patients must lack any active viral infections or active fungal infection. * No appropriate donor * Appropriate cord blood is available: matched at least in 4/6 of A, B, DR loci. * Patients (or one of parents if patients age \< 19) should sign informed consent.

Exclusion criteria

* Pregnant or nursing women. * Malignant or nonmalignant illness that is uncontrolled or whose control may be jeopardized by complications of study therapy. * Psychiatric disorder that would preclude compliance. * Congenital aplastic anemia including Fanconi anemia.

Design outcomes

Primary

MeasureTime frame
To evaluate the engraftment potential of fludarabine, busulfan plus thymoglobulin conditioning regimen for cord blood transplantation (CBT) in severe aplastic anemia.From Oct 2008. to Sep 2011

Secondary

MeasureTime frame
To evaluate overall and event free survival rateFrom Oct 2008. to Sep 2011
To evaluate acute and chronic GVHDFrom Oct 2008. to Sep 2011
To evaluate immunologic recovery after CBTFrom Oct 2008. to Sep 2011
To evaluate the incidence and severity of toxicity and treatment related mortalityFrom Oct 2008. to Sep 2011

Countries

South Korea

Contacts

Primary ContactHyoung Jin Kang, M.D, Ph.D
kanghj@snu.ac.kr82 2 2072 3304
Backup ContactJi Won Lee, M.D
agnesjw@hanmail.net82 2 2072 0177

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026