Overview
Cost-Effectiveness Study of PEG-rhG-CSF in Prophylactic Treatment of Neutropenia After Chemotherapy in Lymphoma
Status:
Recruiting
Recruiting
Trial end date:
2022-04-01
2022-04-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
This is a pharmacoeconomic research to explore the cost-effectiveness of PEG-rhG-CSF and rhG-CSF in prophylactic treatment of neutropenia in lymphoma patients. It should provide more scientific basis for clinical decision-making.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Ruijin Hospital
Criteria
Inclusion Criteria:- 18-65 years
- histologically confirmed de novo Non Hodgkin's lymphoma (except highly aggressive
lymphoma such as lymphoblastic lymphoma and Burkitt lymphoma)
- plan to be given 6-8 cycles of cyclophosphamide, doxorubicin, vincristine, and
prednisone (CHOP) ± Rituximab (R)
- KPS ≥70
- plan continuous PEG-rhG-CSF or rhG-CSF adiministration after at least 3 cycles of
treatment for neutropenia prophylactic treatment
- absolute neutrophil count≥1.5×109/L,platelet count ≥100× 109/L,hemoglobin≥90g/L,while
blood cell count≥3.0×109/L,without bleeding signs
- adquate liver and renal function as protocol discribed
- no serious cardiovascular disease as protocol discribed
- under good mental conditions and informed consented
- potential benefit for subjects based on investigators' decision
Exclusion Criteria:
- history of hematopoetic stem cell transplantationor organ transplantation
- uncontrollable infection
- allergic to study drugs or ingredients
- accepted any other investigational drug or participated another interventional study
within 30 days during screening period
- other uncontrollable conditions judged by the investigator
- breast-feeding , pregnant or plan to be pregnant during study observation period