Skip to main content
Clinical Trials/NCT03304990
NCT03304990
Withdrawn
N/A

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

Greater Baltimore Medical Center1 site in 1 countryNovember 29, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Cancer
Sponsor
Greater Baltimore Medical Center
Locations
1
Primary Endpoint
Panomics Relationships in the Epidemiology of Cancer through In Silico Expression (PRECISE)
Status
Withdrawn
Last Updated
5 years ago

Overview

Brief Summary

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.

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
November 29, 2018
End Date
January 1, 2019
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

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

Time Frame: 5 years

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

Study Sites (1)

Loading locations...

Similar Trials