A Lifetime Partnership With Patients Who Have or May be at Risk of Having Cancer

The Oncology Research Information Exchange Network (ORIEN) hopes to establish a unique
collection of blood, tissue, other biological samples and their associated data (survey data,
medical records data, cancer registry data, and other related data) from thousands of
patients with cancer or at risk of having cancer. Their hope is to, over time, facilitate new
clinical trials, technology, informatics solutions, and personalized medicine to each cancer
patient.

Inclusion Criteria:

1. 18 years of age and older.

2. Diagnosed with cancer, or may be at risk for cancer.

3. Able to understand and sign the TCCP Informed Consent and Research Authorization form
directly or through a legally authorized representative (LAR).

Non-English speaking subjects will also be invited to participate in the TCCP study, in
accordance with COMIRB's short-form consent use.

Exclusion Criteria:

1. Members of vulnerable populations including neonates (birth to 30 days), children (under
age 18), wards of the State, prisoners or those on probation or alternate sentencing, or
decisionally challenged (adults or children that are cognitively impaired, incompetent to
consent, proxy consent, or consenting in life threatening situations).