Racial disparities in prostate cancer in the UK and the USA: similarities, differences and steps forwards.

In the USA, Black men are approximately twice as likely to be diagnosed with and to die of prostate cancer than white men. In the UK, despite Black men having vastly different ancestral contexts and health-care systems from Black men in the USA, the lifetime risk of being diagnosed with prostate cancer is two-to-three times higher among Black British men than among white British men and Black British men are twice as likely to die of prostate cancer as white British men. Examination of racial disparities in prostate cancer in the USA and UK highlights systemic, socio-economic and sociocultural factors that might contribute to these differences. Variation by ancestry could affect incidence and tumour genomics. Disparities in incidence might also be affected by screening guidelines and access to and uptake of screening. Disparities in treatment access, continuity of care and outcomes could contribute to survival differences. In both localized and metastatic settings, equal access could diminish the observed disparities in both the USA and the UK. An understanding of behavioural medicine, especially an appreciation of cultural beliefs about illness and treatment, could inform and improve the ways in which health systems can engage with and deliver care to patients in minoritized groups affected by prostate cancer. Methods of promoting equity include targeting systemic barriers including systemic racism, proportional recruitment of patients into clinical trials, diversifying the health-care workforce and facilitating care informed by cultural humility. Actively engaging patients and communities in research and intervention might enable the translation of research into increasingly equitable care for patients with prostate cancer in the UK, the USA and globally.

Nature reviews. Urology. 2024 Oct 18 [Epub ahead of print]

Edward Christopher Dee, Rebecca Todd, Kenrick Ng, Gloryanne Aidoo-Micah, Troy B Amen, Zoe Moon, Randy Vince, Vinayak Muralidhar, Katherine Mutsvangwa, Garth Funston, Luke T A Mounce, Elias Pintus, Kosj Yamoah, Daniel E Spratt, Brandon A Mahal, Jonathan Shamash, Robert Horne, Paul L Nguyen

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA. ., Department of Practice and Policy, Centre for Behavioural Medicine, University College London School of Pharmacy, London, UK., Department of Medical Oncology, Barts Cancer Centre, London, UK., Department of Medical Oncology, Royal Free Hospital NHS Foundation Trust, London, UK., Department of Orthopedic Surgery, Hospital for Special Surgery, New York, NY, USA., Case Western Reserve University, University Hospital Urology Institute, Cleveland, OH, USA., Department of Radiation Oncology, Kaiser Permanente Northwest, Portland, OR, USA., Clinical Commissioning Group, NHS North East London, London, UK., Centre for Cancer Screening, Prevention and Early Diagnosis, Queen Mary University of London, London, UK., Department of Health and Community Sciences, University of Exeter, St Luke's Campus, Heavitree Road, Exeter, UK., Guy's Cancer Centre, Guy's and St Thomas' NHS Foundation Trust, Great Maze Pond, London, UK., Department of Radiation Oncology, H. Lee Moffitt Cancer Center & Research Institutes, Tampa, FL, USA., Department of Radiation Oncology, Case Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH, USA., Department of Radiation Oncology, University of Miami Miller School of Medicine, Miami, FL, USA., Department of Radiation Oncology, Dana-Farber Cancer Institute/Harvard Cancer Center, Boston, MA, USA.