Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital, 171 76, Stockholm, Sweden.
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Virchows Arch. 2024 Jun;484(6):995-1003. doi: 10.1007/s00428-024-03810-y. Epub 2024 Apr 29.
A 5-tier grouping of Gleason scores has recently been proposed. Studies have indicated prognostic heterogeneity within these groups. We assessed prostate cancer-specific mortality (PCSM) and all-cause mortality (ACM) for men diagnosed with Gleason score 3 + 5 = 8, 4 + 4 = 8 and 5 + 3 = 8 acinar adenocarcinoma on needle biopsy in a population-based national cohort. The Prostate Cancer data Base Sweden 5.0 was used for survival analysis with PCSM and ACM at 5 and 10 years as endpoints. Multivariable Cox regression models controlling for socioeconomic factors, stage and primary treatment type were used for PCSM and ACM. Among 199,620 men reported with prostate cancer in 2000-2020, 172,112 were diagnosed on needle biopsy. In 18,281 (11%), there was a Gleason score of 8 in needle biopsies, including a Gleason score of 3 + 5, 4 + 4 and 5 + 3 in 11%, 86% and 2.3%, respectively. The primary treatment was androgen deprivation therapy (55%), deferred treatment (8%), radical prostatectomy (16%) or radical radiotherapy (21%). PCSM in men with Gleason scores of 3 + 5, 4 + 4 and 5 + 3 at 5 years of follow-up was 0.10 (95% CI 0.09-0.12), 0.22 (0.22-0.23) and 0.32 (0.27-0.36), respectively, and at 10 years 0.19 (0.17-0.22), 0.34 (0.33-0.35) and 0.44 (0.39-0.49), respectively. There was a significantly higher PCSM after 5 and 10 years in men with Gleason score 5 + 3 cancers than in those with 4 + 4 and in Gleason score 4 + 4 cancers than in those with 3 + 5. Grouping of Gleason scores will eliminate the prognostic granularity of Gleason scoring, thus diminishing the prognostic significance of this proposed grading system.
最近提出了一种 5 级 Gleason 评分分组。研究表明,这些组内存在预后异质性。我们评估了在基于人群的全国队列中,经针吸活检诊断为 Gleason 评分 3+5=8、4+4=8 和 5+3=8 腺泡腺癌的男性的前列腺癌特异性死亡率 (PCSM) 和全因死亡率 (ACM)。使用前列腺癌数据库瑞典 5.0 进行生存分析,以 PCSM 和 ACM 在 5 年和 10 年的终点。多变量 Cox 回归模型控制了社会经济因素、分期和主要治疗类型,用于 PCSM 和 ACM。在 2000-2020 年报告的 199620 名男性前列腺癌患者中,172112 名患者经针吸活检诊断。在 18281 名患者 (11%) 中,在针吸活检中存在 Gleason 评分 8,包括 3+5、4+4 和 5+3 的分别为 11%、86%和 2.3%。主要治疗方法为雄激素剥夺疗法 (55%)、延迟治疗 (8%)、根治性前列腺切除术 (16%)或根治性放疗 (21%)。在 5 年随访时,Gleason 评分分别为 3+5、4+4 和 5+3 的男性的 PCSM 分别为 0.10(95%CI 0.09-0.12)、0.22(0.22-0.23)和 0.32(0.27-0.36),在 10 年随访时分别为 0.19(0.17-0.22)、0.34(0.33-0.35)和 0.44(0.39-0.49)。在 Gleason 评分 5+3 癌症患者中,5 年和 10 年后的 PCSM 明显高于 Gleason 评分 4+4 癌症患者,而 Gleason 评分 4+4 癌症患者的 PCSM 又明显高于 Gleason 评分 3+5 癌症患者。Gleason 评分分组将消除 Gleason 评分的预后粒度,从而降低该拟议分级系统的预后意义。