SURGE: Supporting Utility and Representation in Genomics-based cancer trial Enrollment (Intervention)

ENROLLING
Protocol # :
21-709
Conditions
Gastrointestinal Cancer
Hematologic Cancer
Thoracic Cancer
Phase
Not Applicable
Disease Sites
Gastroesophageal Junction
Gallbladder/Biliary
Stomach
Small Intestine
Colon
Other Digestive Organ
Lung
Other Respiratory and Intrathoracic Organs
Prostate
Other Hematopoietic
Non-Hodgkin's Lymphoma
Hodgkin's Lymphoma
Multiple Myeloma
Lymphoid Leukemia
Myeloid and Monocytic Leukemia
Leukemia, other
Principal Investigator
McCleary, Nadine, J

Trial Description

SURGE aims to increase equity in clinical trial enrollment by addressing barriers to
genomic testing, which is increasingly needed to assess precision clinical trial
eligibility and access standard precision therapies. The study is an interventional pilot
meant primarily to assess the feasibility of the intervention. The intervention is
comprised of a patient navigator, text message questionnaire, and informational video.

Eligibility Requirements

Inclusion Criteria:

- Adult (age 18 years or older)

- Black, Latinx, OR older adult (age 70 years or older)

- Scheduled for a new patient consultation

- Suspected or confirmed advanced malignancy (requiring active treatment)

- Gastrointestinal, hematologic, or thoracic cancer

- DFCI patient at Longwood/Chestnut Hill, DFCI satellite at St. Elizabeth's Medical
Center, or DFCI satellite at Merrimack Valley

Exclusion Criteria:

- Malignancy or former malignancy that requires only surveillance

- Not continuing care at a participating DFCI site

- Speaks a language other than English or Spanish

- Unable to provide consent

21-709