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临床试验/NCT01317108
NCT01317108已完成3 期

Adjuvant Chemotherapy in Node-negative Breast Cancer: Chemo N0

Universitätsklinikum Hamburg-Eppendorf0 个研究点目标入组 689 人开始时间: 1993年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
689
主要终点
The benefit of adjuvant chemotherapy in high-risk group according to uPA/PAI-1: Number of patients disease-free vs. those relapsed at the given time points

研究概览

简要总结

Chemo-N0 (1993-1998) is the first prospective randomized multicenter trial in N0 BC designed to prospectively evaluate the clinical utility of a biomarker. It used uPA/PAI 1 as stratification criteria and randomized high-risk patients to chemotherapy versus observation; low-risk patients remained without any systemic therapy. The trial was designed to answer two principle questions:

  1. Can the reported prognostic impact of uPA and PAI 1 be validated in a prospective multicenter therapy trial? Does low uPA/PAI 1 identify those low-risk N0 patients who are candidates for being spared necessity and burden of adjuvant chemotherapy?
  2. Do uPA/PAI 1 high-risk patients benefit from adjuvant CMF chemotherapy?

研究设计

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

入排标准

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

入选标准

  • N0 breast cancer patients tumor size >/= 1 and </= 5 cm in diameter undergoing standard loco-regional treatment

排除标准

  • M1 status

研究组 & 干预措施

B1

Active Comparator

High uPA/PAi-1: CMF chemotherapy

干预措施: CMF Chemotherapy (Drug)

结局指标

主要结局

The benefit of adjuvant chemotherapy in high-risk group according to uPA/PAI-1: Number of patients disease-free vs. those relapsed at the given time points

时间窗: DFS at 3, 5, and 10 years (depending on analysis time point)

Interim analyses planned at 4.5, 6.5, and 8.5 years after first patient in. Final analysis scheduled at 10.5 years after last patient in.

Prognostic impact of uPA/PAI-1: Number of patients disease-free in low vs. high risk groups according to uPA/PAI-1

时间窗: DFS at 3, 5, and 10 years (depending on analysis time point)

Interim analyses planned at 4.5, 6.5, and 8.5 years after first patient in. Final analysis scheduled at 10.5 years after last patient in.

次要结局

  • Overall survival(at 3, 5, and 10 years (depending on analysis time point).)

研究者

申办方类型
Other
责任方
Sponsor

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Prognostic and Predictive Impact of uPA/PAI-1 | 临床试验