Durham Veterans Affairs Health Care System, Department of Surgery, Durham, NC; Department of Urology, University of California - Los Angeles, Los Angeles, CA; Department of Urology, Cedars-Sinai Medical Center, Los Angeles.
Department of Biostatistics and Bioinformatics, Cedars-Sinai Medical Center, Los Angeles, CA.
Urol Oncol. 2024 Jun;42(6):175.e1-175.e8. doi: 10.1016/j.urolonc.2024.02.010. Epub 2024 Mar 15.
To assess whether contemporary risks of biochemical recurrence (BCR) after radical prostatectomy (RP) in the AS era differ from historical estimates due to changes in tumor risk case mix and improvements in risk stratification.
We sampled 6,682 men who underwent RP for clinically localized disease between 2000 and 2017 from the VA SEARCH database. Kaplan Meier analysis was used to calculate incidence of BCR before and after 2010 overall and within tumor risk subgroups. Multivariable Cox proportional hazard regression analysis including an interaction term between era and tumor risk was used to compare risk of BCR before and after 2010 overall and across tumor risk subgroups.
About 3,492 (52%) and 3,190 (48%) men underwent RP before and after 2010, respectively. In a limited multivariable model excluding tumor risk, overall BCR risk was higher post-2010 vs. pre-2010 (HR: 1.15, 95%CI: 1.05-1.25; 40% vs 36% at 8 years post-RP). However, this effect was eliminated after correcting for tumor risk (HR: 0.95, 95%CI: 0.87-1.04), suggesting that differences in tumor risk between eras mediated the change. Yet, within tumor-risk subgroups, BCR risk was significantly lower for favorable intermediate-risk (HR: 0.76, 95%CI:0.60-0.96) and unfavorable intermediate-risk PC (HR: 0.78, 95%CI: 0.67-0.90), but significantly higher for high-risk PC (HR: 1.22, 95%CI: 1.07-1.38) in the post-2010 era. 8-year risks of BCR in the post-2010 era were 21% (95%CI: 16%-25%), 25% (95%CI: 20%-30%), 41% (95%CI: 37%-46%), and 60% (95%CI: 56%-64%) for low-, FIR-, UIR-, and high-risk disease, respectively. Limitations include limited long-term follow-up in the post-2010 subgroup.
Overall BCR risk has increased in the AS era, driven by a higher risk case mix and increased BCR risk among high-risk patients. Physicians should quote contemporary estimates of BCR when counseling patients.
评估在 AS 时代,根治性前列腺切除术 (RP) 后生化复发 (BCR) 的当代风险是否因肿瘤风险病例组合的变化和风险分层的改善而与历史估计值有所不同。
我们从 VA SEARCH 数据库中抽取了 2000 年至 2017 年间接受 RP 治疗局限性疾病的 6682 名男性患者作为样本。使用 Kaplan-Meier 分析计算 2010 年前和后 BCR 的发生率,总体情况以及肿瘤风险亚组内的发生率。使用包括时代和肿瘤风险之间交互项的多变量 Cox 比例风险回归分析,比较 2010 年前和后 BCR 的风险,总体情况以及肿瘤风险亚组内的风险。
分别有 3492 名(52%)和 3190 名(48%)男性在 2010 年前和后接受 RP。在排除肿瘤风险的有限多变量模型中,2010 年后总体 BCR 风险高于 2010 年前(HR:1.15,95%CI:1.05-1.25;RP 后 8 年分别为 40%和 36%)。然而,在纠正肿瘤风险后,这种影响被消除(HR:0.95,95%CI:0.87-1.04),表明肿瘤风险在时代之间的差异介导了这种变化。然而,在肿瘤风险亚组内,低危、中危有利、中危不利和高危 PC 的 BCR 风险分别显著降低(HR:0.76,95%CI:0.60-0.96)和(HR:0.78,95%CI:0.67-0.90),但高危 PC 的 BCR 风险显著升高(HR:1.22,95%CI:1.07-1.38)。2010 年后的 8 年 BCR 风险分别为低危疾病 21%(95%CI:16%-25%)、中危有利 25%(95%CI:20%-30%)、中危不利 41%(95%CI:37%-46%)和高危 60%(95%CI:56%-64%)。
局限性包括 2010 年后亚组的长期随访有限。
在 AS 时代,整体 BCR 风险增加,这是由更高的风险病例组合和高危患者的 BCR 风险增加所驱动的。医生在为患者提供咨询时应引用当代 BCR 的估计值。