Braga Isaac, Gonçalves-Monteiro Salomé, Calisto Rita, Rangel Marta, Medeiros Eduardo, Cunha José Luís, Rosinha Alina, Oliveira Ângelo, Fialho Ana Cristina, Santos Susana, Redondo Patrícia, Bento Maria José
Department of Urology, Portuguese Oncology Institute of Porto/Porto Comprehensive Cancer Centre & Health Research Network@Research Center of Portuguese Oncology Institute of Porto, 4200-072 Porto, Portugal.
Outcomes Research Lab, Portuguese Oncology Institute of Porto, 4200-072 Porto, Portugal.
Oncol Lett. 2024 Jun 7;28(2):362. doi: 10.3892/ol.2024.14495. eCollection 2024 Aug.
Despite the high prevalence of localised prostate cancer (LPC) and locally advanced prostate cancer (LAPC), evidence on the characteristics of patients, treatments and clinical outcomes stratified by disease risk is limited. The PEarlC study was conducted to characterise a cohort of patients with early-stage prostate cancer that included real-world clinical outcomes. Retrospective data from a cohort of patients diagnosed with LPC/LAPC between 2015 and 2017 and followed up until December 2020 at a Portuguese comprehensive cancer centre (IPO Porto) was analysed. Patients were classified as LPC (high- or non-high-risk) or LAPC according to European Association of Urology guidelines, were eligible if diagnosed at stage I-III and followed up in Urology, Medical Oncology or Radiation Oncology outpatient clinics of IPO Porto. Data was collected from the medical/administrative records database. Clinical outcomes included prostate-specific antigen (PSA) progression-free survival, metastasis-free survival, disease-free survival, progression-free survival, overall survival (OS), PSA response (palliative) and no evidence of residual tumour (prostatectomy). Time-to-event outcomes were compared between subgroups using the log-rank test. A total of 790 patients were included (54.8% non-high-risk LPC, 30.9% high-risk LPC, 14.3% LAPC) and the median follow-up was 46.7 months. Patients had a median age of 68.0 years. The majority of patients were stage II (52.9%) and Eastern Cooperative Oncology Group 0-1 (99.9%) and received treatment with curative intent (85.4%). The median was only achieved in progression-free survival (29.9 months; 95% CI, 26.5-41.0 months), as evaluated in palliative patients. At year 5, 82.9% were free of PSA progression (curative), 87.5% were metastasis-free, 83.7% were disease-free, all patients in palliative treatment progressed and the 5-year OS rate was 92.9% (CI 95%, 90.2-95.7%). Among patients with LPC, OS was worse in high-risk vs. non-high-risk patients (5-year OS rate, 88.8% vs. 96.8%; hazard ratio=3.34, CI 95%, 1.64-7.05; P=0.001). PSA response rate was 81.4% in the palliative setting. There was no evidence of residual tumour in 61.6% of patients who underwent prostatectomy. Although most patients with early-stage prostate cancer treated at IPO Porto showed positive 5-year real-world outcomes, patients with high-risk LPC showed worse OS compared with patients with non-high-risk LPC and therefore a poorer prognosis. The present large-sample real-world study is an important contribution to reducing the evidence gap on prostate cancer.
尽管局限性前列腺癌(LPC)和局部晚期前列腺癌(LAPC)的发病率很高,但按疾病风险分层的患者特征、治疗方法和临床结局的证据有限。PEarlC研究旨在对一组早期前列腺癌患者进行特征描述,包括真实世界的临床结局。分析了2015年至2017年间在葡萄牙一家综合癌症中心(波尔图肿瘤研究所)诊断为LPC/LAPC并随访至2020年12月的一组患者的回顾性数据。根据欧洲泌尿外科学会指南,患者被分类为LPC(高危或非高危)或LAPC,在I-III期诊断且在波尔图肿瘤研究所泌尿外科、医学肿瘤学或放射肿瘤学门诊接受随访的患者符合条件。数据从医疗/行政记录数据库中收集。临床结局包括前列腺特异性抗原(PSA)无进展生存期、无转移生存期、无病生存期、无进展生存期、总生存期(OS)、PSA反应(姑息性)和无残留肿瘤证据(前列腺切除术)。使用对数秩检验比较亚组之间的事件发生时间结局。共纳入790例患者(54.8%为非高危LPC,30.9%为高危LPC,14.3%为LAPC),中位随访时间为46.7个月。患者的中位年龄为68.0岁。大多数患者为II期(52.9%)且东部肿瘤协作组状态为0-1(99.9%),并接受了根治性治疗(85.4%)。仅在姑息性患者中评估的无进展生存期达到了中位值(29.9个月;95%CI,26.5-41.0个月)。在第5年,82.9%的患者无PSA进展(根治性),87.5%的患者无转移,83.7%的患者无病,所有接受姑息治疗的患者均出现疾病进展,5年总生存率为92.9%(95%CI,90.2-95.7%)。在LPC患者中,高危患者的总生存期比非高危患者差(5年总生存率,88.8%对96.8%;风险比=3.34,95%CI,1.64-7.05;P=0.001)。姑息治疗中的PSA反应率为81.4%。在接受前列腺切除术的患者中,61.6%没有残留肿瘤的证据。尽管在波尔图肿瘤研究所接受治疗的大多数早期前列腺癌患者显示出良好的5年真实世界结局,但高危LPC患者与非高危LPC患者相比总生存期更差,因此预后更差。这项目前的大样本真实世界研究对缩小前列腺癌证据差距做出了重要贡献。