Skip to content

ATG Combined With Cyclophosphamide And Cord Blood Transfusion in Treating Patients With Severe Aplastic Anemia

Multi-center Clinical Study of Immunosuppressants, Cyclophosphamide, And Cord Blood Transfusion in Treating Patients With Severe Aplastic Anemia

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02838992
Enrollment
130
Registered
2016-07-20
Start date
2017-02-28
Completion date
2019-07-31
Last updated
2017-02-01

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

Conditions

Aplastic Anemia

Keywords

Cyclophosphamide, Umbilical Cord Blood, ATG

Brief summary

To assess whether ATG Combined With Cyclophosphamide and cord blood infusion can accelerate hematopoietic reconstruction in severe aplastic anemia patients and improve clinical curative effect and safety

Detailed description

Aplastic Anemia( AA), is a set of bone marrow hematopoietic dysfunction caused by a variety of causes, with hyperplasia of bone marrow hematopoietic cells to reduce whole blood cells and peripheral blood at the characteristics of clinical main performance for anemia, bleeding and infection. According to the severity of the bone marrow failure and the progress of the clinical course ,it is divided into Severe Aplastic Anemia (SAA) and the Non - Severe Aplastic Anemia (NSAA).Severe Aplastic Anemia can be divided into two categories: Very Severe Aplastic Anemia (VSAA) and Severe Aplastic Anemia (SAA), with the characteristics of rapid progress, refractory, poor prognosis, high mortality .The natural course is six months or so, and most patients die in a year . Hematopoietic stem cell transplantation and immunosuppressive therapy are two main treatment . The former is by far the only possible cure. It is recommended as first-line treatments, if patients have a matched sibling donor. The recommended age limit is 40 years old. But for those who have no sibling donor or patients older than 40 years old, it is recommend the immunosuppressive therapy. The investigators have already summarized the effectiveness of rabbit antithymocyte immunoglobulin (ATG), cyclophosphamide (Cy) and cyclosporine, A (CsA) and the combination of the umbilical cord blood infusion for SAA/VSAA patients without suitable donor, with short duration, without long-term immunosuppressive therapy history. The total effectiveness rates has improved to 88%, with shorter immunosuppressive maintaining therapy , rapid hematopoietic reconstruction, fewer complications. The aim of this study is to further explore whether this solution can accelerate hematopoietic reconstruction of SAA/VSAA patients and its clinical curative effect and security. This study scheme has been approved by the Jinan military region general hospital medical ethics committee.

Interventions

DRUGRabbit ATG, (Genzyme)

ATG is an infusion of rabbit-derived antibodies against human T cells, which is used in the prevention and treatment of acute rejection in organ transplantation and therapy of aplastic anemia

DRUGCy

Cyclophosphamide is a medication mainly used in chemotherapy. It is an alkylating agent of the nitrogen mustard type

DRUGCsA

CsA is an immunosuppressant drug widely used in organ transplantation to prevent rejection. It reduces the activity of the immune system by interfering with the activity and growth of T cells

BIOLOGICALCord blood

Cord blood is blood that remains in the placenta and in the attached umbilical cord after childbirth. Cord blood is collected because it contains stem cells, which can be used to treat hematopoietic and genetic disorders

Sponsors

Shandong University of Traditional Chinese Medicine
CollaboratorOTHER
Jining Medical University
CollaboratorOTHER
Weifang Medical University
CollaboratorOTHER
Guangzhou First People's Hospital
CollaboratorOTHER
Harbin Hematology and Oncology Institute
CollaboratorOTHER
Jining First People's Hospital
CollaboratorOTHER
JIANGXI Provincal People's Hospital
CollaboratorUNKNOWN
Jinhua Central Hospital
CollaboratorOTHER
Linyi People's Hospital
CollaboratorOTHER
Shandong Cord Blood Bank
CollaboratorUNKNOWN
Qingdao Hiser Medical Group
CollaboratorOTHER
Qingdao University
CollaboratorOTHER
Taian City Central Hospital
CollaboratorOTHER
Yantai Yuhuangding Hospital
CollaboratorOTHER
Yishui Central Hospital of LINYI
CollaboratorUNKNOWN
Institute of Hematology & Blood Diseases Hospital, China
CollaboratorOTHER
Shengjing Hospital
CollaboratorOTHER
Jinan Military General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

1. Male or female ,under the age of 60. 2. Diagnosis of SAA and VSAA in accordance with the \<aplastic anemia, diagnosis and treatment expert consensus\> Camitta standard (see appendix 1). 3. Confirmed of heavy and very heavy aplastic anemia within 6 months. 4. No obvious abnormal liver and kidney function: ALT, AST,≤2.5 times the upper limit of normal , serum Creatinine and BUN ≤1.25 times the upper limit of normal 5. Clear understanding, voluntary to participate in the study, and signed informed consent document by the patient or the legal guardian 6. Willingness and ability to comly with the treatment plan, follow-up and laboratory tests as required

Exclusion criteria

1. Congenital aplastic anemia 2. Pregnancy or breastfeeding 3. Participated in other clinical trials within three months 4. Presence of Any fatal disease, including respiratory failure, heart failure, liver or kidney failure, et al 5. Aplastic anemia caused by the treatment of other malignant tumor treatment 6. With severe mental illness 7. With other malignant tumor 8. Severe infection or the infection difficult to be controlled 9. Received ATG or cyclosporine A within six months 10. Severely allergic to biological agents 11. Any other situation judged by the investigator that the patients inappropriate for entry into this study

Design outcomes

Primary

MeasureTime frameDescription
The total response rateEvery 3 months to 24 monthsResponse rate is the ratio of CR and PR patients to all evaluated patients at the time point. CR,PR,NR and relapse is evaluated according to the guidelines for the diagnosis and management of adult aplastic anaemia from British Committee for Standards in Haematology (BCSH)

Secondary

MeasureTime frameDescription
Neutrophil recovery timeFrom day 0 until the first of 3 consecutive daysThe neutrophil recovery day is defined from day 0 until the first of 3 consecutive days during which the absolute neutrophil count (ANC) is \>0.5×10\^9/L, without G-CSF administration .
Infection rates1 year
Overall survival2 years
Treatment related mortality2 years

Countries

China

Contacts

Primary ContactFang Zhou, MD
zhoufang1@medmail.com.cn86-0531-51665316
Backup ContactZhe Yu, MD
doctoryu1120@163.com86-0531-51665781

Outcome results

None listed

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