It is not particularly clear to me how ORIEN will differ from NCCN...is it the manner of data collection and sharing? Will the 2 networks ultimately become identical in participants?
"Nearly 150,000 patients, including almost every OSU cancer patient, have agreed to be part of the database. They donate blood and tumor tissue samples for research studies and consent to make their records available to all ORIEN participants. They also agree to be contacted should a clinical study arise."