Patel Neal A, Barocas Daniel A, Lin Daniel W, Wu Xian, Green David, Kensler Kevin H, Shoag Jonathan, Al Hussein Al Awamlh Bashir
Department of Urology, Weill Cornell Medicine, New York, New York.
Department of Urology, Vanderbilt University Medical Center, Nashville, Tennessee.
JAMA Oncol. 2025 Jul 31. doi: 10.1001/jamaoncol.2025.2304.
Advocates for removing the cancer label from grade group 1 (GG1) prostate cancer detected on biopsy primarily base their argument on the observation that when only GG1 is detected on prostatectomy, rates of metastasis are rare. However, the frequency with which GG1 prostate cancer on biopsy is associated with adverse clinical features and the long-term cancer outcomes in this context are poorly defined.
To assess cancer-specific outcomes of localized GG1 prostate cancer stratified by risk category.
DESIGN, SETTING, AND PARTICIPANTS: A population-based cohort study using Surveillance, Epidemiology, and End Results data was performed to assess cancer-specific outcomes in 117 162 men with localized GG1 prostate cancer stratified by National Comprehensive Cancer Network risk groups between January 1, 2010, and December 31, 2020. Competing risk analyses and multivariable regression determined rates of prostate cancer-specific mortality and associations with prostatectomy adverse pathology. Data were analyzed from July 1, 2024, to October 1, 2024.
Prostate cancer-specific mortality and risk of adverse pathology at surgery in GG1 prostate cancer.
Among 117 162 men with biopsy GG1 prostate cancer, 10 440 (9%) had favorable intermediate-risk disease, 3145 (3%) had unfavorable intermediate-risk disease, and 4539 (4%) had high-risk disease. Median age was 64 years (IQR, 58-69 years). A total of 867 men with high-risk GG1 prostate cancer (60%) had adverse pathology at prostatectomy. The prostate cancer-specific mortality rates for unfavorable intermediate-risk GG1 and for high-risk GG1 were 2.4% and 4.7%, respectively, comparable to the prostate cancer-specific mortality rates for favorable intermediate-risk GG2 and unfavorable intermediate-risk greater than or equal to GG2, which were 2.1% and 4.0%, respectively. In adjusted analyses, favorable intermediate-risk GG1 (adjusted hazard ratio [AHR], 1.60; 95% CI, 1.30-1.96), unfavorable intermediate-risk GG1 (AHR, 2.10; 95% CI, 1.53-2.89), and high-risk GG1 (AHR, 3.58; 95% CI, 2.93-4.38) were associated with increased risk of prostate cancer-specific mortality compared with low-risk GG1.
This cohort study found that approximately 1 in 6 men with GG1 prostate cancer has intermediate-risk or high-risk disease. Biopsy GG1 prostate cancer has heterogeneous long-term outcomes that are reflected in adverse pathology and prostate cancer-specific mortality. These data indicate that not all GG1 prostate cancer follows an indolent course. A subset of men with biopsy GG1 prostate cancer have outcomes comparable to those of men with higher-grade intermediate-risk prostate cancer, a group that often undergoes treatment. These findings should be considered in the reclassification debate.
活检时检测到的1级(GG1)前列腺癌的癌症标签取消倡导者主要基于这样的观察结果来立论,即前列腺切除术中仅检测到GG1时,转移率很低。然而,活检时GG1前列腺癌与不良临床特征相关的频率以及在此背景下的长期癌症结局定义尚不明确。
评估按风险类别分层的局限性GG1前列腺癌的癌症特异性结局。
设计、设置和参与者:使用监测、流行病学和最终结果数据进行了一项基于人群的队列研究,以评估2010年1月1日至2020年12月31日期间117162名局限性GG1前列腺癌男性按美国国立综合癌症网络风险组分层后的癌症特异性结局。竞争风险分析和多变量回归确定了前列腺癌特异性死亡率以及与前列腺切除术后不良病理的关联。数据于2024年7月1日至2024年10月1日进行分析。
GG1前列腺癌的前列腺癌特异性死亡率和手术时不良病理的风险。
在117162名活检为GG1前列腺癌的男性中,10440名(9%)患有有利的中危疾病,3145名(3%)患有不利的中危疾病,4539名(4%)患有高危疾病。中位年龄为64岁(四分位间距,58 - 69岁)。共有867名高危GG1前列腺癌男性(60%)在前列腺切除术中出现不良病理。不利的中危GG1和高危GG1的前列腺癌特异性死亡率分别为2.4%和4.7%,与有利的中危GG2和大于或等于GG2的不利中危的前列腺癌特异性死亡率分别为2.1%和4.0%相当。在多因素分析中,与低危GG1相比,有利的中危GG1(调整后风险比[AHR],1.60;95%置信区间,1.30 - 1.96)、不利的中危GG1(AHR,2.10;95%置信区间,1.53 - 2.89)和高危GG1(AHR,3.58;95%置信区间,2.93 - 4.38)与前列腺癌特异性死亡风险增加相关。
这项队列研究发现,每6名GG1前列腺癌男性中约有1人患有中危或高危疾病。活检GG1前列腺癌具有异质性的长期结局,这在不良病理和前列腺癌特异性死亡率中有所体现。这些数据表明并非所有GG1前列腺癌都呈惰性病程。一部分活检为GG1前列腺癌的男性的结局与中危前列腺癌分级较高的男性相当,而这一群体通常接受治疗。在重新分类的辩论中应考虑这些发现。