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临床试验/NCT04101760
NCT04101760Unknown3 期

Long-acting Versus Short-acting Granulocyte Colony Stimulating Factor for the Prevention of Febrile Neutropenia in Epithelial Ovarian Cancer Patients: A Multicenter Phase 3 Randomized Controlled Study

Lei Li1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2019年10月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
发起方
入组人数
200
试验地点
1
主要终点
Incidence of febrile neutropenia

研究概览

简要总结

This study aims to analyze the effects of long-acting versus short-acting granulocyte colony stimulating factor (G-CSF) on the prevention febrile neutropenia (FN) in epithelial ovarian cancer patients.

Patients receive platinum-based chemotherapy of 3 to 4 weeks. Patients are randomized into study group and control group. In study group, patients accept long-acting G-CSF 48 hours from the chemotherapy. While the control group accept regular or prophylactic treatment of short-acting G-CSF according to National Comprehensive Cancer Network guidelines.

The primary end is the incidence of FN in every course of chemotherapy.

The secondary ends include: the incidences of myelosuppression, doses of G-CSF and its expenses, visits to outpatient and emergency clinics, adverse events related to G-CSF, quality of life, and survival outcomes (progression-free survival and overall survival).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • •With definitive pathological results of epithelial ovarian cancer
  • •With an Eastern Cooperative Oncology Group (ECOG) performance status score of 0-2
  • •Aged 18 or older
  • •Receiving 3-4 weeks per cycle of platinum-based chemotherapy with or without debulking surgery
  • •Regularly followed up in the study centers
  • •Provided consent for participation.

排除标准

  • •Failure to meet all the inclusion criteria
  • •Non-compliance with the study protocols
  • •With a history of chemotherapy or pelvic radiotherapy for malignancies
  • •Presence of immunosuppressive diseases such as organ transplantation or acquired immune deficiency syndrome
  • •Treated with weekly chemotherapy regimens
  • •Presence of hematological disorders

研究组 & 干预措施

Study group

Experimental

Patients in study group accept prophylactic treatment of long-acting granulocyte colony stimulating factor

干预措施: Long-acting granulocyte colony stimulating factor (Drug)

Control group

Active Comparator

Patients in control group accept regular or prophylactic treatment of short-acting granulocyte colony stimulating factor according to current guidelines

干预措施: Short-acting granulocyte colony stimulating factor (Drug)

结局指标

主要结局

Incidence of febrile neutropenia

时间窗: One year

Incidence of febrile neutropenia during each course of chemotherapy

次要结局

  • Adverse events(One years)
  • Progression-free survival(Two years)
  • Overall survival(Two years)
  • Incidence of myelosuppression(One year)
  • Doses of granulocyte colony stimulating factor(One year)
  • Numbers of visits to the hospital(One year)

研究者

发起方
Lei Li
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Lei Li

Professor

Peking Union Medical College Hospital

研究点 (1)

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