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临床试验/NCT02270931
NCT02270931已完成不适用

A Prospective Longitudinal Study of CA 15-3 as an Aid in Monitoring Recurrence or Progressive Disease in Patients With Breast Cancer

Fujirebio Diagnostics, Inc.3 个研究点 分布在 1 个国家目标入组 130 人开始时间: 2014年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
130
试验地点
3
主要终点
Measure CA 15-3 in Breast Cancer Patients

研究概览

简要总结

The purpose of this study is to obtain sufficient specimens and correlating clinical data from a well-controlled prospective clinical trial collecting longitudinal specimens from subjects diagnosed with any stage of breast cancer.

详细描述

The study objectives are described below:

  1. Obtain serum and plasma specimens longitudinally collected from a minimum of 130 subjects diagnosed with breast cancer and are about to or are currently undergoing treatment and follow-up. Specimens will be used to evaluate CA 15-3 assays, currently under development, as an aid for monitoring recurrence or progressive disease.
  2. To store any remaining specimens for use in future cancer research and to evaluate as yet undetermined biomarkers for the development of IVDs, including additional CA 15-3 assays, for monitoring the course of disease and therapy in subjects diagnosed with breast cancer.

研究设计

研究类型
Observational
观察模型
Cohort
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

  • Males and females, age≥ 18 years
  • Histologic/pathologic confirmation of breast cancer
  • Any stage of disease: Newly diagnosed, stable, disease progression, surveillance
  • Any treatment time point: Treatment naïve, currently receiving or completed therapy for breast cancer including active monitoring.
  • Individuals with a history of malignant disease other than breast cancer that was resected greater than 5 years ago and are currently in remission are eligible.
  • Able to understand and willing to provide informed consent

排除标准

  • Males and females, age <18 years
  • No histologic/pathologic confirmation of breast cancer
  • Any concurrent malignancy other than basal or squamous cell skin cancers, in-situ cervical cancer, or breast cancer.
  • Treatment plan with fewer than three visits expected in 3 years' time
  • Unable to provide informed consent

结局指标

主要结局

Measure CA 15-3 in Breast Cancer Patients

时间窗: 3 years

130 patients with Recurrence or Progressive Breast Cancer.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (3)

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