Murray Nigel P, Fuentealba Cinthia, Reyes Eduardo, Salazar Anibal, Guzman Eghon, Orrego Shenda
Facultad de Medicina. Universidad Finis Terrae. Providencia. Santiago. Chile. Departamento de Medicina. Hospital de Carabineros de Chile. Ñuñoa. Santiago. Chile.
Departamento de Urología. Hospital de Carabineros de Chile. Ñuñoa. Santiago. Chile.
Arch Esp Urol. 2021 Jul;74(6):554-563.
To compare the classification CAPRA (based on clinical-pathological findings) and minimal residual disease (MRD) (based on biological characteristics) to predict biochemical failure (BF).
The clinical-pathological findings of the prostate biopsy were used to determine the CAPRA score, classifying patients into low, intermediate and high risk. Blood and bone marrow samples to detect circulating prostate cells (CPCs) and micro-metastasis were taken. The samples were classified as positive if ≥1 prostate cell was detected, forming three subgroups; Group A (MRD negative), Group B (micro-metastasis positive, CPC negative) and Group C (CPC positive). Patients were followed-up for 10 yearsor BF. Kaplan-Meier biochemical failure free survival (BFFS) curves, a predictive flexible parameter survival model and mean restricted survival times (MRST) were determined.
347 men participated, BF risk increased with increasing CAPRA score, HR 1.21 intermediate, 1.64 high risk; versus MRD HR 1.91 and 4.43 for Groups Band C. After 10 years the BFFS and MRST were 76%, 50% and 17% and 9, 7 and 5 years respectively for CAPRA versus 94%, 57% and 26% and 10, 9 and 6 years respectively for MRD. The concordance between observed and predicted BFFS was acceptable for CAPRA (Harrell´s C 0.64) and very good (0.92) for MRD. The BFFS curves for MRD were not proportional with time, they were similar for 5 years for Groups A and B, with increasing BFFS in Group B there after.The CAPRA score did not distinguish between Groups A and B, one third of low risk CAPRA patients had CPCs detected.
The MRD classification was superior to CAPRA, differentiating between early and late failure.
比较基于临床病理结果的CAPRA分类和基于生物学特征的微小残留病(MRD),以预测生化复发(BF)。
前列腺活检的临床病理结果用于确定CAPRA评分,将患者分为低、中、高风险组。采集血液和骨髓样本以检测循环前列腺细胞(CPC)和微转移。如果检测到≥1个前列腺细胞,则样本分类为阳性,形成三个亚组;A组(MRD阴性)、B组(微转移阳性,CPC阴性)和C组(CPC阳性)。对患者进行10年随访或直至发生BF。确定Kaplan-Meier无生化复发生存率(BFFS)曲线、预测性灵活参数生存模型和平均受限生存时间(MRST)。
347名男性参与研究,BF风险随CAPRA评分增加而增加,中风险组HR为1.21,高风险组HR为1.64;而MRD中B组和C组的HR分别为1.91和4.43。10年后,CAPRA的BFFS和MRST分别为76%、50%和17%以及9年、7年和5年,而MRD分别为94%、57%和26%以及10年、9年和6年。CAPRA观察到的和预测的BFFS之间的一致性尚可(Harrell's C为0.64),而MRD的一致性非常好(0.92)。MRD的BFFS曲线与时间不成比例,A组和B组在5年内相似,此后B组的BFFS增加。CAPRA评分无法区分A组和B组,三分之一的低风险CAPRA患者检测到CPC。
MRD分类优于CAPRA,可区分早期和晚期复发。