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临床试验/NCT02178475
NCT02178475已完成不适用

Prospective Observational Study of Febrile Neutropenia (FN) and Pegfilgrastim Primary Prophylaxis in Breast Cancer and Non-Hodgkin's Lymphoma Patients Receiving High (>20%) FN-risk Chemotherapy

Amgen1 个研究点 分布在 1 个国家目标入组 943 人开始时间: 2014年7月18日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Amgen
入组人数
943
试验地点
1
主要终点
Percentage of Participants With Febrile Neutropenia

研究概览

简要总结

To estimate the incidence of febrile neutropenia in patients with breast cancer and non-Hodgkin's lymphoma receiving high (> 20%) FN-risk chemotherapy and pegfilgrastim primary prophylaxis.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

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

入选标准

  • Age ≥ 18 years old.
  • Any stage NHL or breast cancer and received the first cycle of a new chemotherapy course.
  • Received the first cycle of a permitted standard dose chemotherapy regimens with an estimated high (> 20%) FN risk according to published data or guidelines (dose modifications +/-10% in Cycle 1 are allowable).
  • Initiated treatment in Cycle 1 with pegfilgrastim according to the pegfilgrastim summary of product characteristics. (SmPC). Enrolment must occur after the first pegfilgrastim dosing in Cycle 1 and before the second day of Cycle 2.

排除标准

  • Ongoing or planned concurrent participation in any clinical study involving Investigational Product that has not been approved by the national competent authorities for any indication.
  • Ongoing or planned concurrent participation in any clinical study where the administration of Colony Stimulating Factor (CSF) is determined by the protocol (clinical trials on an approved drug and observational trials are permitted as long as these do not mandate how neutropenia should be treated).

结局指标

主要结局

Percentage of Participants With Febrile Neutropenia

时间窗: Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.

Febrile neutropenia (FN) was defined as an absolute neutrophil count (ANC) of \< 0.5 x 10\^9/L, or \< 1.0 x 10\^9/L predicted to fall below 0.5 x 10\^9/L within 48 hours with fever or clinical signs of sepsis; fever and ANC were measured the same day or within ± 1 calendar day.

次要结局

  • Number of Participants Who Discontinued Pegfilgrastim Prophylaxis(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Reasons for Discontinuation of Pegfilgrastim Prophylaxis(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Reasons for Discontinuation of G-CSF Prophylaxis(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Number of Participants Who Permanently Switched From Pegfilgrastim Prophylaxis to Other G-CSF Prophylaxis(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Characteristics of Participants Who Discontinued G-CSF Prophylaxis(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Number of Cycles With No G-CSF Prophylaxis in Which Febrile Neutropenia Events Occurred(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Number of Febrile Neutropenia Events That Occurred During Cycles With No G-CSF Prophylaxis(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Number of Participants Who Experienced Febrile Neutropenia During Cycles With No G-CSF Prophylaxis(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Characteristics of Participants Who Received On-schedule Pegfilgrastim Primary Prophylaxis(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Number of Participants Who Discontinued G-CSF Prophylaxis(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Number of Cycles With no G-CSF Prophylaxis(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Percentage of Participants Who Experienced Complications of Febrile Neutropenia(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Number of Participants Who Experienced Complications of Febrile Neutropenia During Cycles With No G-CSF Prophylaxis(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Characteristics of Participants Who Discontinued Pegfilgrastim Prophylaxis(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Number of Cycles With No Pegfilgrastim Prophylaxis(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)
  • Number of Cycles With No G-CSF Prophylaxis in Which Complications of Febrile Neutropenia Occurred(Participants were followed for up to 8 cycles of chemotherapy; the average observation time was 4.1 months.)

研究者

发起方
Amgen
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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