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Prophylactic administration of mecapegfilgrastim after chemotherapy in patients with lymphoma

Prophylactic administration of mecapegfilgrastim after chemotherapy in patients with lymphoma

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100048123
Enrollment
Unknown
Registered
2021-07-03
Start date
2018-01-01
Completion date
Unknown
Last updated
2022-03-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Febrile Neutropenia

Interventions

Sponsors

Shanxi Tumor Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients with HL or NHL who received at least one cycle of chemotherapy were enrolled. All patients signed informed consent forms. Aged >=18 years; the ability to complete at least one cycle of chemotherapy as planned (patients with an intermediate risk of FN needed to have more than one risk factor); a normal bone marrow hematopoietic function with no bleeding tendency; absolute neutrophil count (ANC) >=2.0x10^9/L, serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) <=1.5 ULN, serum total bilirubin (TBIL) <=1.5 ULN, serum creatinine (Scr) <=1.5 ULN.

Exclusion criteria

Exclusion criteria: Presence of acute infection and receipt of systemic anti-infection treatment in the 72 hours before chemotherapy; presence of hematological diseases affecting the hematopoietic function of bone marrow; patients who had bone marrow or stem-cell transplantation within the past 3 months; presence of other uncured or brain metastatic malignant tumors; presence of allergic reaction or intolerance to the study drugs; presence of mental or nervous system disorders; women who were pregnant or breast feeding; women of childbearing age who refused contraceptive use; patients who had previously received PEG-rhG-CSF; and some special cases that the investigators determined should be excluded.

Design outcomes

Secondary

MeasureTime frame
Biochemicaltests;

Primary

MeasureTime frame
ANC;

Countries

China

Contacts

Public ContactSu Liping

Shanxi Tumor Hospital

sulp@163.com+86 13834141851

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026