Buelens Sarah, Poelaert Filip, Dhondt Bert, Fonteyne Valérie, De Visschere Pieter, Ost Piet, Verbeke Sofie, Villeirs Geert, De Man Kathia, Rottey Sylvie, Decaestecker Karel, Lumen Nicolaas
Department of Urology, Ghent University Hospital, Ghent, Belgium; Department of Radiation Oncology and Experimental Cancer Research, Cancer Research Institute Ghent, Ghent University, Ghent, Belgium.
Department of Urology, Ghent University Hospital, Ghent, Belgium; Department of Radiation Oncology and Experimental Cancer Research, Cancer Research Institute Ghent, Ghent University, Ghent, Belgium.
Urol Oncol. 2018 Apr;36(4):158.e13-158.e20. doi: 10.1016/j.urolonc.2017.12.009. Epub 2018 Jan 12.
No uniformity exists in the definition of metastatic burden in metastatic hormone-naive prostate cancer (mHNPC) across clinical trials making their comparison challenging. We explored definition agreement and prognostic significance of bulky mHNPC according to the CHAARTED and LATITUDE trial.
Since 2014, 95 patients with newly diagnosed mHNPC were prospectively registered. For this study, they were categorized as having high-volume (HVD) vs. low-volume (LVD) and high-risk (HRD) vs. low-risk disease (LRD) according to the definition of CHAARTED and LATITUDE, respectively. Agreement was tested using Cohen's κ coefficient. The Kaplan-Meier method was used to compare castration-resistant prostate cancer-free survival (CRPC-FS) and overall survival (OS). Prognostic significance was analyzed using Cox regression models.
In total, 44 (46%) and 46 (48%) patients showed HVD and HRD, respectively. Cohen's κ coefficient was 0.83 indicating "almost perfect" agreement (P<0.001). Median CRPC-FS was 40 (95% CI: 25-55) vs. 11 months (95% CI: 8-14) for LVD and HVD (P = 0.001); 40 (95% CI: 27-53) vs. 11 months (95% CI: 8-14) for LRD and HRD (P<0.001), respectively. Median OS was not reached vs. 51 months (95% CI: 0-102) for LVD and HVD (P = 0.001); not reached vs. 51 months (95% CI: 2-100) for LRD and HRD (P = 0.003), respectively. The prognostic significance of both definitions remained significant in the multivariate model for CRPC-FS (P = 0.012 and P = 0.003).
There is an excellent agreement between the definitions of bulky mHNPC in the CHAARTED and LATITUDE trial. Both definitions have significant prognostic value for predicting worse CRPC-FS and OS.
在转移性激素初治前列腺癌(mHNPC)中,转移性负担的定义在各项临床试验中并不统一,这使得它们之间的比较具有挑战性。我们根据CHAARTED和LATITUDE试验探讨了大块mHNPC的定义一致性和预后意义。
自2014年起,前瞻性登记了95例新诊断的mHNPC患者。在本研究中,根据CHAARTED和LATITUDE的定义,分别将他们分为高体积(HVD)与低体积(LVD)以及高风险(HRD)与低风险疾病(LRD)。使用Cohen's κ系数检验一致性。采用Kaplan-Meier方法比较去势抵抗性前列腺癌无进展生存期(CRPC-FS)和总生存期(OS)。使用Cox回归模型分析预后意义。
总共44例(46%)和46例(48%)患者分别表现为HVD和HRD。Cohen's κ系数为0.83,表明“几乎完美”的一致性(P<0.001)。LVD和HVD的CRPC-FS中位数分别为40个月(95%CI:25-55)和11个月(95%CI:8-14)(P = 0.001);LRD和HRD的CRPC-FS中位数分别为4个月(95%CI:27-53)和11个月(95%CI:8-14)(P<0.001)。LVD和HVD的OS中位数未达到,而LVD为51个月(95%CI:0-102)(P = 0.001);LRD和HRD的OS中位数未达到,而LRD为51个月(95%CI:2-100)(P = 0.003)。在CRPC-FS的多变量模型中,两种定义的预后意义均仍然显著(P = 0.012和P = 0.003)。
CHAARTED和LATITUDE试验中大块mHNPC的定义之间具有极好的一致性。两种定义对于预测较差的CRPC-FS和OS均具有显著的预后价值。