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Race, tumor location, and disease progression among low‐risk prostate cancer patients

BACKGROUND: The relationship between race, prostate tumor location, and BCR‐free survival is inconclusive. This study examined the independent and joint roles of patient race and tumor location on biochemical recurrence‐free (BCR) survival. METHODS: A retrospective cohort study was conducted among m...

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Detalles Bibliográficos
Autores principales: Mygatt, Justin G., Cullen, Jennifer, Streicher, Samantha A., Kuo, Huai‐Ching, Chen, Yongmei, Young, Denise, Gesztes, William, Williams, Grant, Conti, Galen, Porter, Christopher, Stroup, Sean P., Rice, Kevin R., Rosner, Inger L., Burke, Allen, Sesterhenn, Isabell
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064097/
https://www.ncbi.nlm.nih.gov/pubmed/31965751
http://dx.doi.org/10.1002/cam4.2864
Descripción
Sumario:BACKGROUND: The relationship between race, prostate tumor location, and BCR‐free survival is inconclusive. This study examined the independent and joint roles of patient race and tumor location on biochemical recurrence‐free (BCR) survival. METHODS: A retrospective cohort study was conducted among men with newly diagnosed, biopsy‐confirmed, NCCN‐defined low risk CaP who underwent radical prostatectomy (RP) at the Walter Reed National Military Medical Center from 1996 to 2008. BCR‐free survival was modeled using Kaplan‐Meier estimation curves and multivariable Cox proportional hazards (PH) analyses. RESULTS: There were 539 eligible patients with low‐risk CaP (25% African American, AA; 75% Caucasian American, CA). Median age at CaP diagnosis and post‐RP follow‐up time was 59.2 and 8.1 years, respectively. Kaplan‐Meier analyses showed no significant association between race (P = .52) or predominant tumor location (P = .98) on BCR‐free survival. In Cox PH multivariable analysis, neither race (HR = 1.18; 95% CI = 0.68‐2.02; P = .56) nor predominant tumor location (HR = 1.13; 95% CI = 0.59‐2.15; P = .71) was an independent predictor of BCR‐free survival. CONCLUSIONS: Neither race nor predominant tumor location was associated with adverse oncologic outcome.