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临床试验/NCT02944604
NCT02944604已完成4 期

The Efficacy and Safety of PEG-rhG-CSF(Pegylated Recombinant Human Granulocyte Colony Stimulating Factor)in Patients With Breast Cancer Who Were Treated With Intensive Chemotherapy

Peking University1 个研究点 分布在 1 个国家目标入组 240 人开始时间: 2016年9月8日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
240
试验地点
1
主要终点
Incidence of chemotherapy delay

研究概览

简要总结

The purpose of the study is to evaluate the efficacy and safety of PEG-rhG-CSF in patients with breast cancer who were treated with intensive chemotherapy for prevention of neutrophil reduction.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 1.18-65 years old, gender no limited.
  • 2.Breast cancer diagnosed by pathology.
  • 3.Did not receive chemotherapy previously and plans to receive 4 cycles intensive EC (epirubicin, cyclophosphamide) treatment.
  • 4.No obvious blood system disease, ANC(absolute neutrophil count)≥ 1.5 × 10^9/L, PLT(Platelet)≥80×10^9 /L, Hb(hemoglobin)≥75g/L, WBC(White blood cell )≥3×109/L, and no bleeding tendency.
  • 5.KPS (Karnofsky performance status) score≥
  • 6.Expected survival≥3 months.
  • 7.Written informed consent are acquired.

排除标准

  • Severe or uncontrolled infection.
  • Sensitive to the product or other genetically engineered biological products from Escherichia coli strains.
  • Mental or nervous system disorders.
  • Severe heart, lung and central nervous system disorders.
  • Pregnant or lactating women.
  • TBIL(total bilirubin ), ALT(alanine aminotransferase),AST(glutamic-oxalacetic transaminase) > 2.5×ULN(upper limit of normal); if it were caused by liver metastases, TBIL, ALT,AST >5×ULN.
  • Cr(creatinine) >1.5×ULN.

研究组 & 干预措施

PEG-rhG-CSF

Experimental

Patients with breast cancer who were treated with intensive chemotherapy received PEG-rhG-CSF.

干预措施: PEG-rhG-CSF (Drug)

结局指标

主要结局

Incidence of chemotherapy delay

时间窗: 60 days after the first chemotherapy

次要结局

未报告次要终点

研究者

发起方
Peking University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Tao OUYANG

Chairman of Breast Center

Peking University

研究点 (1)

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