[Federal Register: February 25, 1999 (Volume 64, Number 37)] [Notices] [Page 9337-9338] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr25fe99-72] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Government-Owned Inventions; Availability for Licensing AGENCY: National Institutes of Health, Public Health Service, DHHS. ACTION: Notice. ----------------------------------------------------------------------- SUMMARY: The invention listed below is owned by an agency of the U.S. Government and is available for licensing in the U.S. in accordance with 35 U.S.C. 207 to achieve expeditious commercialization of results of federally funded research and development. ADDRESS: Licensing information and a copy of the U.S. patent application referenced below may be obtained by contacting J.R. Dixon, Ph.D., at the Office of Technology Transfer, National Institutes of Health, 6011 Executive Boulevard, Suite 325, Rockville, Maryland 20852- 3804 (telephone 301/496-7056 ext 206; fax 301/402-0220; E-Mail: jd212g@NIH.GOV). A signed Confidential Disclosure Agreement is required to receive a copy of any patent application. Entitled: Methods for Determining the Prognosis of Breast Cancer Using Antibodies Specific for Thymidylate Synthase Inventors: Drs. Patrick G. Johnston (NCI) and Carmen J. Allegra (NCI), Serial No. 09/152,647 filed 14 September 1998. Thymidylate synthase provides the sole de novo source of thymidylate for DNA synthesis. It is also a critical therapeutic target for the fluoropyrimidine cytotoxic drugs, such as fluorouracil (``5- FU'') and flurodeoxyureidine (``FudR''). In pre-clinical and clinical studies increased expression of thymidylate synthase protein has been associated with resistance to 5-FU. The quantitation of thymidylate synthase has traditionally been performed using enzymatic biochemical assays; however, these assays have major limitations when applied to human tumor tissue samples. Recently, monoclonal antibodies have been developed to human thymidylate synthase that have the required sensitivity and specificity to detect and quantitate thymidylate synthase enzyme in formalin-fixed tissue sections. Hence, this invention provides a method for determining the prognosis of a patient afflicted with breast cancer, by obtaining a solid breast tumor tissue sample, measuring the level of thymidylate synthase expression in the [[Page 9338]] tissue sample using antibody specific for thymidylate synthase. This invention further provides a method for predicting the benefit of chemotherapy for a patient afflicted with breast cancer. The above mentioned invention is derived from the discovery that high thymidylate synthase expression is associated with a poor prognosis in node- positive, but not in node-negative, breast cancer patients. Further, with some 2,504 patients, thymidylate synthase expression was not found to be correlated with other prognostic factors including tumor size, ER status, PR Status, tumor grade, vessel invasion, and histology. The above mentioned invention is available for licensing on an exclusive or non-exclusive basis. Dated: February 16, 1999. Jack Spiegel, Director, Division of Technology Development and Transfer, Office of Technology Transfer. [FR Doc. 99-4658 Filed 2-24-99; 8:45 am] BILLING CODE 4140-01-M