| Literature DB >> 33531479 |
Matthew P Goetz1,2, Keith L Knutson3, Nadine Norton4, Bahaaeldin Youssef5, David W Hillman6, Aziza Nassar7, Xochiquetzal J Geiger7, Brian M Necela5, Heshan Liu6, Kathryn J Ruddy1, Mei-Yin C Polley6, James N Ingle1, Fergus J Couch6,8, Edith A Perez9, Minetta C Liu1,8, Jodi M Carter8, Roberto A Leon-Ferre1, Judy C Boughey10, Elizabeth B Somers11, Krishna R Kalari6, Daniel W Visscher8.
Abstract
Triple negative breast cancer (TNBC) comprises 15-20% of all invasive breast cancer and is associated with a poor prognosis. As therapy options are limited for this subtype, there is a significant need to identify new targeted approaches for TNBC patient management. The expression of the folate receptor alpha (FRα) is significantly increased in patients with TNBC and is therefore a potential biomarker and therapeutic target. We optimized and validated a FRα immunohistochemistry method, specific to TNBC, to measure FRα expression in a centrally confirmed cohort of 384 patients with TNBC in order to determine if expression of the protein is associated with invasive disease-free survival (IDFS) and overall survival (OS). The FRα IHC demonstrated exceptional performance characteristics with low intra- and interassay variability as well as minimal lot-to-lot variation. FRα expression, which varied widely from sample to sample, was detected in 274 (71%) of the TNBC lesions. In a multivariable model adjusted for baseline characteristics, FRα expression was associated with improved IDFS (HR = 0.63, p = 0.01) but not with OS. The results demonstrate the potential of targeting the FRα in the majority of TNBC patients and suggest that variable expression may point to a need to stratify on FRα expression in clinical studies.Year: 2020 PMID: 33531479 DOI: 10.1038/s41523-020-0147-1
Source DB: PubMed Journal: NPJ Breast Cancer ISSN: 2374-4677