PEG-rhG-CSF in Lymphoma Patients After Autologous Hematopoietic Stem Cell Transplantation

Peking University96 enrolled

Overview

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.

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Lymphoma

Interventions

PEG-rhG-CSFDRUG

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.

rhG-CSFDRUG

rhG-CSF was given day +1 after transplantation with a dose of 5μg/kg once per day

Eligibility

Sex: ALLMin age: 18 YearsMax age: 65 Years

Medical Language ↔ Plain English

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. \-

Locations (1)

Peking University Cancer Hospital

Beijing, China

RECRUITING

Outcomes

Primary Outcomes

Time to neutrophil engraftment

Time frame: 30days

Central Contacts

Jun Zhu, MD

CONTACT

+86-10-88196596 zj@bjcancer.org

Data from ClinicalTrials.gov

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