Clinical and Laboratory Analysis of Familial Cancer

National Cancer Institute (NCI)

Status: Completed

Conditions: Cancer

Study type: Observational

Funder types: NIH

Identifiers

NCT02565004

150204

15-C-0204

Details and patient eligibility

About

Background:

DNA makes up the instruction book for people s cells. Cancer is a disease caused by DNA changes that build up and affect cell function. Researchers want to learn more about what may cause cancer by testing the DNA of people with the disease and their family members.

Objective:

To find DNA changes that may be inherited and may cause or influence whether a person gets cancer. To study families with clusters of cancer to find out if there is a DNA mutation specific to certain cancers.

Eligibility:

People 18 years of age and older who:

Participated in the familial genetic part of NIH study 09-C-0079, a previous study or had family members enrolled in this study

Design:

Participants may have been screened in the previous study. They will give permission for researchers to use their data and their tissue or blood samples collected in the study.

Participants may give blood samples.

At each stage of testing, participants will meet with a genetics health care provider. The provider will explain the tests and answer questions.

If researchers find a DNA change that might increase the risk for cancer or other health issues, they will confirm this result in a testing lab. This will require a blood sample.

Participants personal DNA data and health information will be put in a database for research purposes.

Full description

Background:

• This study is to continue the analysis begun on 09C0079 which was focused on identification of the genetic mutation associated with a new gastric polyposis syndrome, Gastric Adenocarcinoma and Proximal Polyposis of the Stomach (GAPPS).
• GAPPS is an autosomal dominant gastric polyposis syndrome that confers a substantial risk for gastric adenocarcinoma and has been found to be associated with germline point variants in APC promoter 1B.
• At this time, any non-gastric phenotype associated with GAPPS is unknown and is being explored using a phenotyping survey interview.

Objective

• To specifically investigate families with clusters of cancer to determine if there is a potential familial genetic mutation specific to a particular cancer and if present, to compare these genetic abnormalities with individuals from the same family without cancer.

Eligibility:

• Participants must meet one of the following:

  • Have been previously enrolled on the familial genetic analysis arm of NIH study 09-C-0079; OR
  • Be family members of patients previously enrolled on the familial genetic analysis arm of 09-C-0079; OR
  • Have a documented pathogenic germline APC promotor 1B variant from a CLIA approved laboratory.

• Participants must be 10 years of age or older

Design:

• This protocol was originally opened to continue same use of research that was approved under protocol 09-C-0079, to analyze the data for publication, and to provide participants with any results of clinical and analytic validity and clinical utility.
• In a subsequent amendment carriers of a germline APC promoter 1B variant will participate in a phenotyping assessment survey interview to assess the phenotype of Gastric Adenocarcinoma and Proximal Polypopsis of the Stomach (GAPPS).

Enrollment: 19 patients

Sex: All

Ages: 10+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

• INCLUSION CRITERIA:

• Participants must meet one of the following:

  • Have been previously enrolled on the familial genetic analysis arm of NIH study 09-C-0079; OR
  • Be family members of patients previously enrolled on the familial genetic analysis arm of 09-C-0079; OR
  • Have a documented pathogenic germline APC promotor 1B variant from a CLIA approved laboratory.

• Participants must be 10 years of age or older

EXCLUSION CRITERIA:

Inability to provide informed consent.

Trial design

19 participants in 2 patient groups

1

Description:

Patients who were enrolled on protocol 09-C-0079, or family members of patients who were enrolled on protocol 09-C-0079

2

Description:

Individuals found to harbor a germline APC promoter 1B variant not previously enrolled in Cohort l.