Lymphoma
Conditions
Brief summary
The purpose of the study is to evaluate the efficacy and safety of PEG-rhG-CSF on the recovery of hematopoietic function after autologous stem cell transplantation in patients with lymphoma.
Detailed description
At present, there is few related research of Recombinant Human Granulocyte Colony-stimulating Factor applying to AHSCT in China. The purpose of the study is to evaluate the efficacy and safety of PEG-rhG-CSF in lymphoma patients after autologous hematopoietic stem cell transplantation. Eligible patients were randomly assigned to PEG-rhG-CSF group or rhG-CSF group. Patients in PEG-rhG-CSF group received PEG-rhG-CSF day +1 after transplantation with a dose of 100μg/kg. Patients with the weight more than 45kg were suggested a dose of 6 mg. Patients in control group received rhG-CSF day +1 after transplantation with a dose of 5μg/kg once per day until the recovery of neutrophil.
Interventions
DRUGPEG-rhG-CSF
PEG-rhG-CSF was given day +1 after autologous stem cell transplantation with a dose of 100μg/kg(bw).For patients more than 45kg, 6mg was suggested.
DRUGrhG-CSF
rhG-CSF was given day +1 after transplantation with a dose of 5μg/kg once per day
Sponsors
Peking University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
1. Patients with age between 18 and 65 years. 2. Lymphoma patients with the requirement for autologous hematopoietic stem cell transplantation. 3. The collected CD34+ cells≥1×10E6/kg. 4. ECOG score ≤2. 5. Heart and lung is normal. 6. Blood creatinine ≤1.5×ULN. 7. ALT, AST, TBIL ≤2 ×ULN 8. Not in pregnancy. 9. Written informed consent are acquired.
Exclusion criteria
1. Had received autologous hematopoietic stem cell transplantation or allogeneic transplantation. 2. Severe or uncontrolled infectious diseases: HIV, HCV, syphilis, ALT, chronic hepatitis B. 3. Serious complications, such as severe infection, heart, lung, liver and kidney dysfunction. 4. LVEF \<55%. 5. Allergic to the product or other biological products from genetically engineered Escherichia coli strains. 6. Refused to take contraceptive measures during the study period and the subsequent 1 years. 7. Severe mental or neurological disorders. 8. Serious heart, lung, central nervous system disorders. 9. Sickle cell anemia, hemolytic anemia and other hematologic diseases. 10. Participate in other drugs clinical trials 30 days before the screening. 11. Other situation that investigators consider as contra-indication for this study. \-
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time to neutrophil engraftment | 30days |
Countries
China
Contacts
Primary ContactJun Zhu, MD
Outcome results
None listed