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临床试验/NCT03304990
NCT03304990撤回不适用

Panomics Relationships in the Epidemiology of Cancer Through In Silico Expression (PRECISE)

Greater Baltimore Medical Center1 个研究点 分布在 1 个国家开始时间: 2018年11月29日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Panomics Relationships in the Epidemiology of Cancer through In Silico Expression (PRECISE)

研究概览

简要总结

PRECISE is a study to discover new detection, prognosis and treatment biomarkers for cancer. This is a prospective, multi-center, observational study designed to collect de-identified biospecimens and clinical data from a large cohort of participants from clinical research networks in the United States. In this study, the investigators propose creating a large-scale normalized panomics dataset specifically designed for deep learning-based in silico analysis for biomarker discovery.

详细描述

This study will enroll all subjects who are eligible and willing to participate with a goal of enrolling at least 10,000 in several categories: (i) Patients with Family History of Cancer, (ii) Patients with Clinical and Environmental Risk Factors for Cancer, and (iii) Patients with a Suspected or Confirmed Diagnosis of 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

  • Patients with Family History of Cancer
  • Ages 18 or older
  • Either of the following:
  • Patients with two or more first, second or third degree blood relatives on the same side of the family diagnosed with cancer
  • Patients with one or more first, second or third degree blood relative with male breast cancer
  • Patients with a first, second, or third degree blood relative with a known BRCA1 or BRCA2 mutation
  • Patients with a first, second, or third degree blood relative who has had colorectal or endometrial cancer diagnosed before age 50 years
  • Patients with first degree relatives with a known deleterious APC, MEN1, MUTYH, PTEN, RET, STK11, TP53, or VHL gene mutation
  • Patients of Ashkenazi Jewish descent with one or more first degree relatives or two or more second degree relatives with breast, ovarian or colorectal cancer
  • The patient has signed the appropriate Institutional Review Board approved Informed Consent Form
  • Patients with Clinical & Environmental Risk Factors for Cancer
  • Either of the following:
  • Women 21 or older
  • Men 75-85, with a history of smoking
  • At least one guideline recommended cancer screening test documented in the medical record, if indicated for age and gender (eg, pap smear, mammography, low dose chest CT and/or colonoscopy)
  • The patient has signed the appropriate Institutional Review Board approved Informed Consent Form Cancer Patients
  • Ages 18 or older
  • Either of the following:
  • New diagnosis of histologically confirmed cancer (any stage I-IV, as well as carcinoma in situ (CIS)), across multiple solid tumor types with no prior systemic cancer therapy and scheduled for surgical resection or non-surgical management
  • Or, subjects with a high suspicion for cancer diagnosis by clinical and radiological assessment, but without preceding histologic diagnosis, are eligible, if they have not received prior systemic cancer therapy and are scheduled for surgery
  • Has or will have a medically obtained pathological tumor specimen from core needle or surgical biopsy and/or surgical resection within 4 weeks (28 days) of study blood draw and pre-treatment
  • The patient has signed the appropriate Institutional Review Board approved Informed Consent Form

排除标准

  • Blood or blood product transfusion in the preceding 2 months
  • Cognitive impairment as determined by clinical history
  • Pregnant women (by self-report of pregnancy status)
  • Inability to speak English
  • Previous diagnosis of cancer except: non-melanomatous skin cancer
  • Poor health status or unfit to tolerate blood draw

结局指标

主要结局

Panomics Relationships in the Epidemiology of Cancer through In Silico Expression (PRECISE)

时间窗: 5 years

● Discover and validate new detection, prognosis and treatment biomarkers for cancer

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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