This study is a randomized controlled, open and multi-center clinical study. Patients who meet the selection criteria and do not meet the exclusion criteria are randomly given PEG-rhG-CSF with a fixed dose of 12mg when white blood cells reach the lowest point, or given rhG-CSF with a daily mobilization of 5-10μ g/kg until the collection is completed, so as to evaluate the effectiveness and safety of PEG-rhG-CSF in mobilizing autologous stem cells for lymphoma and multiple myeloma.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
174
Subcutaneous injection with a fixed dose of 12 mg
Inject rhG-CSF 5-10 μg/kg subcutaneously every day
Chongqing University Cancer Hospital
Chongqing, Chongqing Municipality, China
RECRUITINGThe proportion of patients with CD34+ cells ≥2×106/kg
The proportion of patients with CD34+ cells ≥2×106/kg
Time frame: 28 days
CD34+cell count
CD34+cell count
Time frame: 28 days
Acquisition times
The number of times a patient needs to collect a sufficient number of CD34+ cells
Time frame: 28 days
Mobilization time
Time interval from mobilization to collection
Time frame: 28 days
Hematopoietic reconstruction time after transplantation
Hematopoietic reconstruction time after transplantation
Time frame: 3 months
complication
complication
Time frame: 3 months
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