PMID- 36993723 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230529 DP - 2023 Mar 16 TI - The Impact of Race and Age on Response to Neoadjuvant Therapy and Long-Term Outcomes in Black and White Women with Early-Stage Breast Cancer. LID - rs.3.rs-2667554 [pii] LID - 10.21203/rs.3.rs-2667554/v1 [doi] AB - PURPOSE: There are a paucity of data and a pressing need to evaluate response to neoadjuvant chemotherapy (NACT) and determine long-term outcomes in young Black women with early-stage breast cancer (EBC). METHODS: We analyzed data from 2,196 Black and White women with EBC treated at the University of Chicago over the last 2 decades. Patients were divided into groups based on race and age at diagnosis: Black women 40 years, White women 40 years, Black women 55 years, and White women 55 years. Pathological complete response rate (pCR) was analyzed using logistic regression. Overall survival (OS) and disease-free survival (DFS) were analyzed using Cox proportional hazard and piecewise Cox models. RESULTS: Young Black women had the highest risk of recurrence, which was 22% higher than young White women (p=0.434) and 76% higher than older Black women (p=0.008). These age/racial differences in recurrence rates were not statistically significant after adjusting for subtype, stage, and grade. In terms of OS, older Black women had the worst outcome. In the 397 women receiving NACT, 47.5% of young White women achieved pCR, compared to 26.8% of young Black women (p=0.012). CONCLUSIONS: Black women with EBC had significantly worse outcomes compared to White women in our cohort study. There is an urgent need to understand the disparities in outcomes between Black and White breast cancer patients, particularly in young women where the disparity in outcome is the greatest. FAU - Terman, Elizabeth AU - Terman E AUID- ORCID: 0000-0002-7378-4171 AD - Pritzker School of Medicine, The University of Chicago. FAU - Sheade, Jori AU - Sheade J AD - Department of Medicine, Section of Hematology and Oncology, The University of Chicago. FAU - Zhao, Fangyuan AU - Zhao F AD - Department of Public Health Sciences, The University of Chicago. FAU - Howard, Frederick M AU - Howard FM AD - Department of Medicine, Section of Hematology and Oncology, The University of Chicago. FAU - Jaskowiak, Nora AU - Jaskowiak N AD - Department of Surgery, The University of Chicago. FAU - Tseng, Jennifer AU - Tseng J AD - Department of Surgery, City of Hope Orange County. FAU - Chen, Nan AU - Chen N AD - Department of Medicine, Section of Hematology and Oncology, The University of Chicago. FAU - Hahn, Olwen AU - Hahn O AD - Department of Medicine, Section of Hematology and Oncology, The University of Chicago. FAU - Fleming, Gini AU - Fleming G AD - Department of Medicine, Section of Hematology and Oncology, The University of Chicago. FAU - Huo, Dezheng AU - Huo D AD - Department of Public Health Sciences, The University of Chicago. FAU - Nanda, Rita AU - Nanda R AUID- ORCID: 0000-0001-5248-0876 AD - Department of Medicine, Section of Hematology and Oncology, The University of Chicago. LA - eng GR - R25 CA240134/CA/NCI NIH HHS/United States PT - Preprint DEP - 20230316 PL - United States TA - Res Sq JT - Research square JID - 101768035 UIN - Breast Cancer Res Treat. 2023 Apr 29;:. PMID: 37120458 PMC - PMC10055663 COIS- Competing Interests Dr. Nanda has received funding from Arvinas, AstraZeneca, Celgene, Corcept Therapeutics, Genentech/Roche, Gilead/Immunomedics, Merck, OBI Pharma, OncoSec, Pfizer, Relay, Seattle Genetics, Sun Pharma, Taiho. She serves on the advisory board of AstraZeneca, BeyondSpring, Fujifilm, GE, Gilead, Infinity, iTeos, Merck, OBI, Oncosec, Sanofi, Seagen. Dr. Fleming serves as an institutional PI of an industry sponsored study for Roche, Iovance, Sermonix, Campugen, Celldex, Corcept, AstraZeneca, Molecular Templates, Astellas, K group beta, and Pfizer. The following companies supported a CME event organized by Dr. Fleming: DSI, Merck, Caris, Eisai, AZ. The remaining authors have no relevant financial or non-financial interests to disclose. EDAT- 2023/03/31 06:00 MHDA- 2023/03/31 06:01 PMCR- 2023/03/29 CRDT- 2023/03/30 02:54 PHST- 2023/03/31 06:01 [medline] PHST- 2023/03/30 02:54 [entrez] PHST- 2023/03/31 06:00 [pubmed] PHST- 2023/03/29 00:00 [pmc-release] AID - rs.3.rs-2667554 [pii] AID - 10.21203/rs.3.rs-2667554/v1 [doi] PST - epublish SO - Res Sq [Preprint]. 2023 Mar 16:rs.3.rs-2667554. doi: 10.21203/rs.3.rs-2667554/v1.