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

Primary Purpose

Aplastic Anemia

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Rabbit ATG, (Genzyme)
Cy
CsA
Cord blood
Sponsored by
Jinan Military General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Aplastic Anemia focused on measuring Cyclophosphamide, Umbilical Cord Blood, ATG

Eligibility Criteria

1 Year - 60 Years (Child, Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • The General Hospital Of Jinan Military Command

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

ATG, Cy and cord blood transfusion group

ATG and CSA group

Arm Description

ATG 3mg/kg/d for 5 days Cy 50mg/kg/d for 2 days CSA Started from 5mg/kg/d and adjusted to maintain trough serum concentration of 200-400ng/ml One unit of cord blood having no more than 3 HLA-A,B and DRB1 mismatches is transfused 24h after last dose of ATG administration. Intervention: Drug: Rabbit ATG, Thymoglobuline (Genzyme) plus Cyclophosphamide plus CSA Biological: Cord blood transfusion

ATG 3mg/kg/d for 5 days CSA started from 5mg/kg/d and adjusted to maintain trough serum concentration of 200-400ng/ml Intervention: Drug: Rabbit ATG, Thymoglobuline (Genzyme) plus CSA

Outcomes

Primary Outcome Measures

The total response rate
Response 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 Outcome Measures

Neutrophil recovery time
The 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 rates
Overall survival
Treatment related mortality

Full Information

First Posted
July 6, 2016
Last Updated
January 31, 2017
Sponsor
Jinan Military General Hospital
Collaborators
Shandong University of Traditional Chinese Medicine, Jining Medical University, Weifang Medical University, Guangzhou First People's Hospital, Harbin Hematology and Oncology Institute, Shandong Jining No.1 People's Hospital, JIANGXI Provincal People's Hospital, Jinhua Central Hospital, Linyi People's Hospital, Shandong Cord Blood Bank, Qingdao Hiser Medical Group, Qingdao University, Taian City Central Hospital, Yantai Yuhuangding Hospital, Yishui Central Hospital of LINYI, Institute of Hematology & Blood Diseases Hospital, China, Shengjing Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02838992
Brief Title
ATG Combined With Cyclophosphamide And Cord Blood Transfusion in Treating Patients With Severe Aplastic Anemia
Official Title
Multi-center Clinical Study of Immunosuppressants, Cyclophosphamide, And Cord Blood Transfusion in Treating Patients With Severe Aplastic Anemia
Study Type
Interventional

2. Study Status

Record Verification Date
January 2017
Overall Recruitment Status
Unknown status
Study Start Date
February 2017 (Anticipated)
Primary Completion Date
December 2018 (Anticipated)
Study Completion Date
July 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Jinan Military General Hospital
Collaborators
Shandong University of Traditional Chinese Medicine, Jining Medical University, Weifang Medical University, Guangzhou First People's Hospital, Harbin Hematology and Oncology Institute, Shandong Jining No.1 People's Hospital, JIANGXI Provincal People's Hospital, Jinhua Central Hospital, Linyi People's Hospital, Shandong Cord Blood Bank, Qingdao Hiser Medical Group, Qingdao University, Taian City Central Hospital, Yantai Yuhuangding Hospital, Yishui Central Hospital of LINYI, Institute of Hematology & Blood Diseases Hospital, China, Shengjing Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aplastic Anemia
Keywords
Cyclophosphamide, Umbilical Cord Blood, ATG

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
130 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ATG, Cy and cord blood transfusion group
Arm Type
Experimental
Arm Description
ATG 3mg/kg/d for 5 days Cy 50mg/kg/d for 2 days CSA Started from 5mg/kg/d and adjusted to maintain trough serum concentration of 200-400ng/ml One unit of cord blood having no more than 3 HLA-A,B and DRB1 mismatches is transfused 24h after last dose of ATG administration. Intervention: Drug: Rabbit ATG, Thymoglobuline (Genzyme) plus Cyclophosphamide plus CSA Biological: Cord blood transfusion
Arm Title
ATG and CSA group
Arm Type
Active Comparator
Arm Description
ATG 3mg/kg/d for 5 days CSA started from 5mg/kg/d and adjusted to maintain trough serum concentration of 200-400ng/ml Intervention: Drug: Rabbit ATG, Thymoglobuline (Genzyme) plus CSA
Intervention Type
Drug
Intervention Name(s)
Rabbit ATG, (Genzyme)
Other Intervention Name(s)
Thymoglobuline, Anti-thymoeyteGlobulin
Intervention Description
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
Intervention Type
Drug
Intervention Name(s)
Cy
Other Intervention Name(s)
Cyclophosphamide, Cytophosphane
Intervention Description
Cyclophosphamide is a medication mainly used in chemotherapy. It is an alkylating agent of the nitrogen mustard type
Intervention Type
Drug
Intervention Name(s)
CsA
Other Intervention Name(s)
Ciclosporin A, Cyclosporine
Intervention Description
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
Intervention Type
Biological
Intervention Name(s)
Cord blood
Other Intervention Name(s)
Umbilical cord blood
Intervention Description
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
Primary Outcome Measure Information:
Title
The total response rate
Description
Response 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)
Time Frame
Every 3 months to 24 months
Secondary Outcome Measure Information:
Title
Neutrophil recovery time
Description
The 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 .
Time Frame
From day 0 until the first of 3 consecutive days
Title
Infection rates
Time Frame
1 year
Title
Overall survival
Time Frame
2 years
Title
Treatment related mortality
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female ,under the age of 60. Diagnosis of SAA and VSAA in accordance with the <aplastic anemia, diagnosis and treatment expert consensus> Camitta standard (see appendix 1). Confirmed of heavy and very heavy aplastic anemia within 6 months. 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 Clear understanding, voluntary to participate in the study, and signed informed consent document by the patient or the legal guardian Willingness and ability to comly with the treatment plan, follow-up and laboratory tests as required Exclusion Criteria: Congenital aplastic anemia Pregnancy or breastfeeding Participated in other clinical trials within three months Presence of Any fatal disease, including respiratory failure, heart failure, liver or kidney failure, et al Aplastic anemia caused by the treatment of other malignant tumor treatment With severe mental illness With other malignant tumor Severe infection or the infection difficult to be controlled Received ATG or cyclosporine A within six months Severely allergic to biological agents Any other situation judged by the investigator that the patients inappropriate for entry into this study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fang Zhou, MD
Phone
86-0531-51665316
Email
zhoufang1@medmail.com.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Zhe Yu, MD
Phone
86-0531-51665781
Email
doctoryu1120@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fang Zhou, MD
Organizational Affiliation
The General Hospital Of Jinan Military Command
Official's Role
Study Chair
Facility Information:
Facility Name
The General Hospital Of Jinan Military Command
City
Jinan
State/Province
Shandong
ZIP/Postal Code
250031
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fang Zhou, MD
Phone
86-0531-51665316
Email
zhoufang1@medmail.com.cn
First Name & Middle Initial & Last Name & Degree
Zhe Yu, MD
Phone
86-0531-51665781
Email
doctoryu1120@163.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
26568159
Citation
Killick SB, Bown N, Cavenagh J, Dokal I, Foukaneli T, Hill A, Hillmen P, Ireland R, Kulasekararaj A, Mufti G, Snowden JA, Samarasinghe S, Wood A, Marsh JC; British Society for Standards in Haematology. Guidelines for the diagnosis and management of adult aplastic anaemia. Br J Haematol. 2016 Jan;172(2):187-207. doi: 10.1111/bjh.13853. Epub 2015 Nov 16. No abstract available. Erratum In: Br J Haematol. 2016 Nov;175(3):546.
Results Reference
background
PubMed Identifier
21663651
Citation
Zhou F, Ge L, Yu Z, Fang Y, Kong F. Clinical observations on intensive immunosuppressive therapy combined with umbilical cord blood support for the treatment of severe aplastic anemia. J Hematol Oncol. 2011 Jun 10;4:27. doi: 10.1186/1756-8722-4-27.
Results Reference
result
PubMed Identifier
24838091
Citation
Xie LN, Fang Y, Yu Z, Song NX, Kong FS, Liu XM, Zhou F. Increased immunosuppressive treatment combined with unrelated umbilical cord blood infusion in children with severe aplastic anemia. Cell Immunol. 2014 May-Jun;289(1-2):150-4. doi: 10.1016/j.cellimm.2014.03.014. Epub 2014 Apr 3.
Results Reference
result
PubMed Identifier
25932194
Citation
Yu Z, Zhou F, Ge LF, Liu XM, Fang Y, Xie LN, Kong FS, Song NX, Yu QQ. Mechanism of immunosuppressants combined with cord blood for severe aplastic anemia. Int J Clin Exp Med. 2015 Feb 15;8(2):2484-94. eCollection 2015.
Results Reference
result
PubMed Identifier
26622526
Citation
Xie LN, Zhou F. Unexpected unrelated umbilical cord blood stem cell engraft in two patients with severe aplastic anemia that received immunosuppressive treatment: A case report and literature review. Exp Ther Med. 2015 Oct;10(4):1563-1565. doi: 10.3892/etm.2015.2698. Epub 2015 Aug 21.
Results Reference
result

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

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