FOR PHYSICIANS

CHANGE HAPPENS
WHEN WE ALL
WORK TOGETHER

When it comes to curing cancer, the power is in the numbers. Not one oncologist or clinic can do it alone. Joining our national effort helps patients, advances cancer research, and builds the unified oncology database that is needed.

HELP BUILD A NATIONAL ONCOLOGY DATABASE THAT BENEFITS EVERYONE.

A SHARED EFFORT

Working together as an oncology community
We can build something more powerful than anything we could build as individuals. Shared data increases research potential and value to advance care.

A PARTNERSHIP MODEL

Clinics are treated as partners Partner clinics directly access data for research. They also share in any net revenue the data provides. There is transparency in data sharing and usage.

AN INNOVATIVE AND POWERFUL PROTOCOL AND DATABASE

Data must be complete and accurate Data must be collected in the right manner to be valuable. ROOT and its associated case report forms, data dictionary, molecular classification, data entry portal, training, and clinical flow provide regulatory-grade data.

PATIENT CONSENT

Patients are asked to participate This protects them and ensures all data sharing is compliant with new privacy laws. Patients can be contacted about further research opportunities.
JOIN THE EFFORT TODAY.