作者
Kerri Beckmann,Aida Santaolalla,Jozien Helleman,Peter R. Carroll,Byung Ha Chung,Lui Shiong Lee,Antoinette S. Perry,J. Rubio‐Briones,Mikio Sugimoto,Bruce J. Trock,Riccardo Valdagni,Prokar Dasgupta,Mieke Van Hemelrijck,Oussama Elhage,Bruce J. Trock,Behfar Ehdaie,Peter R. Carroll,Christopher P. Filson,Christopher J. Logothetis,Todd M. Morgan,Laurence Klotz,Tom Pickles,Eric Hyndman,Caroline M. Moore,Vincent J. Gnanapragasam,Mieke Van Hemelrijck,Prokar Dasgupta,Chris H. Bangma,Monique J. Roobol,Arnauld Villers,G. Robert,Axel Semjonow,Antti Rannikko,Riccardo Valdagni,Antoinette S. Perry,Jonas Hugosson,J. Rubio‐Briones,Anders Bjartell,Lukas Hefermehl,Lee Lui Shiong,Mark Frydenberg,Phillip D. Stricker,Mikio Sugimoto,Byung Ha Chung,Theo van der Kwast,Wim van der Linden,Tim Hulsen,Boris Ruwe,Peter van Hooft,Ewout Steyerberg,Daan Nieboer,Kerri Beckmann,Brian T. Denton,Andrew Hayen,Paul C. Boutros,Wei Guo,Nicole Benfante,Janet E. Cowan,Dattatraya Patil,Lauren Park,Stephanie Ferrante,Alexandre Mamedov,Vincent Lapointe,Trafford Crump,Vasilis Stavrinides,Jenna Kimberly-Duffell,Aida Santaolalla,Daan Nieboer,Jonathan Olivier,T. Rancati,Helén Ahlgren,Juanma Mascarós,Annica Löfgren,Kurt Lehmann,Chin‐Chung Lin,Thomas W. Cusick,Hiromi Hirama,Kwang Suk Lee,Guido Jenster,Anssi Auvinen,Anders Bjartell,Masoom A. Haider,Kees van Bochove,Michelle M. Kouspou,Kellie Paich,Chris H. Bangma,Monique J. Roobol,Jozien Helleman
摘要
Studies of active surveillance (AS) for prostate cancer (PCa) have focussed predominantly on Caucasian populations. Little is known about the experience of Asian men, while suitability for men of African descent has been questioned.To compare baseline characteristics, follow-up, and outcomes for men on AS for PCa, according to ethnicity.The study cohort included 13 centres from the GAP3 consortium that record ethnicity (categorised broadly as Caucasian/white, African/Afro-Caribbean/black, Asian, mixed/other, and unknown). Men with biopsy grade group >2, prostate-specific antigen (PSA) >20 ng/ml, T stage ≥cT3, or age >80 yr were excluded.Clinical characteristics, follow-up schedules, outcome status, and reasons for discontinuation were compared across ethnic groups. Risk of upgrading, potential disease progression (grade group ≥3 or T stage ≥3), suspicious indications (any upgrading, number of positive cores >3, T stage ≥cT3, PSA >20 ng/ml, or PSA density >0.2 ng/ml/cc2), and conversion to treatment were assessed using mixed-effect regression models.The eligible cohort (n = 9158) comprised 83% Caucasian men, 6% men of African descent, 5% Asian men, 2% men of mixed/other ethnicity, and 4% men of unknown ethnicity. Risks of suspicious indicators (hazard ratio = 1.27; 95% confidence interval [CI] 1.12-1.45), upgrading (odds ratio [OR] = 1.40; 95% CI 1.14-1.71), and potential progression (OR = 1.46; 95% CI 1.06-2.01) were higher among African/black than among Caucasian/white men. Risk of transitioning to treatment did not differ by ethnicity. More Asian than Caucasian men converted without progression (42% vs 26%, p < 0.001). Heterogeneity in surveillance protocols and racial makeup limit interpretation.This multinational study found differences in the risk of disease progression and transitioning to treatment without signs of progression between ethnic groups. Further research is required to determine whether differences are due to biology, sociocultural factors, and/or clinical practice.This international study compared prostate cancer active surveillance outcomes by ethnicity. Risks of upgrading and disease progression were higher among African than among Caucasian men. Transitioning to treatment without progression was highest among Asian men. Understanding of these differences requires further investigation.