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临床试验/NCT02608346
NCT02608346已完成不适用

Circulating Tumor DNA and Follow-up of BRCA1 Mutation Carriers (CirCa 01)

Institut Curie8 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2014年11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
200
试验地点
8
主要终点
Sensitivity of plasma TP53 mutation detection as a test to detect any tumor growth (relapse and/or new tumor) during the follow-up of women known to carry BRCA1 germline mutation

研究概览

简要总结

BRCA1 carriers who are at high risk of developing either a relapse and/or a new cancer growth will be included. These patients will be followed up during 30 months (2,5 years) with mutated TP53 mutation detection or during 42 months (3,5 years) with mutated TP53 mutation detection and circulating tumor cells detection (CTC) performed at each hospital visit (for technical reason only patients included at Institut Curie will be proposed to participate to the CTC substudy).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • Patient with no evidence of any invasive tumor mass at inclusion (clinical and, if any, radiological exams)
  • Carriers of known germline BRCA1 deleterious mutation (a personal history of cancer is NOT mandatory).
  • Age ≥ 30 years for patient with personal previous history of cancer
  • Age ≥ 40 years for patient without personal previous history of cancer
  • Patient who a follow-up visit is scheduled in the including center at least once a year
  • Patient having health care insurance
  • Signed informed consent by patient

排除标准

  • Patient presenting with invasive tumor masses (e.g. stage IV cancer or localized cancer not yet surgically removed)
  • Carriers of germline BRCA1 variant of unknown significance
  • Carriers of germline BRCA2 deleterious mutation or variant
  • Individuals with a low risk of BRCA1-related tumor growth, i.e. women who underwent prophylactic bilateral mastectomy AND adnexectomy.
  • Any medical or other condition that in the Investigator's opinion rendered the patient unsuitable for this study
  • Patient deprived from ability to decide on her own.
  • Patient unable to have a regular follow up for geographical, social or psychological reasons.

结局指标

主要结局

Sensitivity of plasma TP53 mutation detection as a test to detect any tumor growth (relapse and/or new tumor) during the follow-up of women known to carry BRCA1 germline mutation

时间窗: Up to 42 months

Sensitivity = % of patients with detectable levels of mutated TP53 ctDNA among those who experience a new tumor growth (relapse and/or new tumor).

Specificity of plasma TP53 mutation detection as a test to detect any tumor growth (relapse and/or new tumor) during the follow-up of women known to carry BRCA1 germline mutation

时间窗: Up to 42 months

Specificity = % of patients with undetectable levels of mutated TP53 ctDNA among those who don't experience a new tumor growth (diagnosed within 6 months after the blood draw).

次要结局

  • Specificity of circulating tumor cells detection as a test to detect any tumor growth (relapse and/or new tumor) during the follow-up of women known to carry BRCA1 germline mutation(Up to 42 months)
  • Positive predictive value for circulating tumor cells(Up to 42 months)
  • Positive predictive value for mutated TP53 ctDNA(Up to 42 months)
  • Sensitivity of circulating tumor cells detection as a test to detect any tumor growth (relapse and/or new tumor) during the follow-up of women known to carry BRCA1 germline mutation(Up to 42 months)
  • Negative predictive value for circulating tumor cells(Up to 42 months)
  • Negative predictive value for mutated TP53 ctDNA(Up to 42 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (8)

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