“…Based on this prior experience, as well as that of the Australasian Oncofertility registry, 36 FertiPROTEKT registry, 37 and Japanese FP registry, 38 in an effort to create a central repository for U.S. data regarding patients who have undergone OTC, the PIN Research Committee has decided to proceed with an effort to create a central repository for data regarding patients who have undergone OTC by: (1) revising all OTC data collection sheets into an updated centralized database to maximize information collected regarding the specifics of treatment, surgery, endocrine function, and obstetrical outcomes; (2) transitioning the database to a centralized site where there is institutional support for this endeavor with a research coordinator, database manager, designated legal team, and local grant funding for the longevity of the program; and (3) promoting vigorous academic output by encouraging each participating site to take ownership and submit research ideas, commit to participating in the chosen research idea, and have equal opportunity for authorship on every publication resulting from the database.…”