Nuclear Medicine Unit, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Department of Health Sciences (DISSAL), University of Genoa, Genoa, Italy.
Eur J Nucl Med Mol Imaging. 2024 Feb;51(3):864-870. doi: 10.1007/s00259-023-06490-z. Epub 2023 Nov 8.
Phase III evidence showed that next-generation imaging (NGI), such as prostate-specific membrane antigen positron emission tomography/computed tomography (PSMA PET/CT), provides higher diagnostic accuracy than bone scan and contrast-enhanced computed tomography (conventional imaging, CI) in the primary staging of intermediate-to-high-risk prostate cancer (PCa) patients. However, due to the lack of outcome data, the introduction of NGI in routine clinical practice is still debated. Analysing the oncological outcome of patients upstaged by NGI (though managed according to CI) might shed light on this issue, supporting the design of randomised trials comparing the effects of treatments delivered based on NGI vs. CI.
We prospectively enrolled a cohort of 100 biopsy-proven intermediate-to-high-risk PCa patients staged with CI and PSMA PET/CT (though managed according to the CI stage), to assess the frequency of the stage migration phenomenon. Stage migration was then assessed as biochemical recurrence-free survival (bRFS) predictor.
Three patients were lost at follow-up after imaging. PSMA PET/CT upstaged 26.8% of patients compared to CI, while it downstaged 6.1% of patients. Notably, 50% of patients excluded from surgery due to the presence of bone metastases at CI would have been treated with radical-intent approaches if PSMA PET/CT had guided the treatment choice. After a median follow-up of 6 months of surgically treated patients, 22/83 (26.5%) had biochemical recurrence (BCR). PSMA PET/CT-driven upstaging determined a significant risk increase for BCR (HR:3.41, 95%CI:1.21-9.56, p = 0.019). Including stage migration in a univariable and multivariable model identified PSMA PET/CT-upstaging as an independent predictor of bRFS.
In conclusion, implementing NGI for staging purposes improves the prediction of bRFS. Although phase III evidence is still needed, this advancement suggests that NGI may better identify patients who would benefit from local treatments than those who may achieve better oncological outcomes through systemic treatment.
III 期证据表明,下一代成像(NGI),如前列腺特异性膜抗原正电子发射断层扫描/计算机断层扫描(PSMA PET/CT),在中高危前列腺癌(PCa)患者的初始分期中,比骨扫描和对比增强计算机断层扫描(常规成像,CI)提供更高的诊断准确性。然而,由于缺乏结局数据,NGI 在常规临床实践中的引入仍存在争议。分析因 NGI 而升级(尽管根据 CI 进行管理)的患者的肿瘤学结局可能有助于解决这个问题,为比较基于 NGI 与 CI 的治疗效果的随机试验设计提供支持。
我们前瞻性纳入了一组 100 名经活检证实的中高危 PCa 患者,这些患者接受 CI 和 PSMA PET/CT 分期(尽管根据 CI 分期进行管理),以评估分期迁移现象的频率。然后,将分期迁移评估为生化无复发生存(bRFS)的预测因素。
在影像学检查后有 3 名患者失访。与 CI 相比,PSMA PET/CT 将 26.8%的患者分期升级,而将 6.1%的患者分期降级。值得注意的是,如果 PSMA PET/CT 指导治疗选择,那么由于 CI 存在骨转移而被排除手术的 50%的患者将接受根治性治疗。在接受手术治疗的患者中位随访 6 个月后,83 名患者中有 22 名(26.5%)出现生化复发(BCR)。PSMA PET/CT 驱动的分期升级显著增加了 BCR 的风险(HR:3.41,95%CI:1.21-9.56,p=0.019)。在单变量和多变量模型中纳入分期迁移,确定 PSMA PET/CT 分期升级是 bRFS 的独立预测因素。
总之,实施 NGI 进行分期可提高 bRFS 的预测准确性。尽管仍需要 III 期证据,但这一进展表明,NGI 可能比 CI 更好地识别出那些通过局部治疗受益更多的患者,而不是那些通过系统治疗获得更好肿瘤学结局的患者。