跳至主要内容
临床试验/NL-OMON23853
NL-OMON23853已完成未知

Development of a more sensitive method to predict breast cancer recurrence after 5-years of endocrine treatment making use of diagnostic leukapheresis to detect circulating tumor cells

KWF0 个研究点目标入组 87 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
87

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational non invasive

入排标准

年龄范围
18 至 64(—)

入选标准

  • 1. Female 2. Age >18 years 3. Diagnosed with ER+ Her2-negative lymph node positive, primary breast cancer 4. Received at least 4.5 - 5.5 years of adjuvant ET for breast cancer including those who are <6 months after finishing endocrine therapy. 5. No clinical signs of locoregional or distant recurrence. 6. At least one adequate peripheral vein in both arms as access for leukapheresis. 7. Provided written informed consent.

排除标准

  • 1. Prior non-breast malignancies <5 years of inclusion, except for basal or squamous cell carcinoma of the skin 2. Pre-existing lymphedema, quantified by specialist 3. Known hypersensitivity to the used anticoagulant (ACD) 4. Inadequate cardiac function or severe cardiovascular comorbidity (heart failure NYHA class III/IV) 5. Coagulation disorders as defined by one of the following: NOTE: the use of all types of anticoagulant therapy is permitted o Coagulation disorder in medical history o Platelet count < 40 x 109/L; Patients not on anticoagulant therapy which affects PT or APTT if: o PT > 1.5 x ULN or PT-INR > 1.5 x ULN o APTT > 1.5 x ULN Patients who take anticoagulant therapy which affects PT or APTT if: o PT or APTT > 1.5 x the upper limit of the desired therapeutic window o Total bilirubin > 2.5 x ULN 6. BMI = 35 kg/m2

研究者

发起方
KWF

相似试验

Development of a more sensitive method to predict... | 临床试验