Public reporting burden for this collection of information is estimated to average 1 hour per response, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing this collection of information. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden to Washington Headquarters Services, Directorate for Information Operations and Reports, 1215 Jefferson Davis Highway, Suite 1204, Arlington. VA 22202-4302, and During the past year, we obtained IRB approval from the DOD to begin data collection in December, 2001. However, the practice of the Breast Health Center, where the study was planned, had changed. Because randomization of patients according to core biopsy scheduling was no longer, we had a series of meetings with the Breast Health Center and Siteman Cancer Center administrators. At these discussions, we decided to revise the protocol. The revised protocol is submitted. Patients will still be randomized into different groups based on the informed consent process, but the timing of the core biopsy would not be manipulated. We still plan to collect observational data on this variable, however. Currently, we are seeking IRB approval of the revised protocol. Once this protocol is approved by the IRB's of both Washington University and DOD, we can begin data collection. The revision of the protocol has led to significant delays in the second phase of this project.