Geboers Bart, Gondoputro William, Thompson James E, Reesink Daan J, van Riel Luigi A M J G, Zhang David, Blazevski Alexandar, Doan Paul, Agrawal Shikha, Matthews Jayne, Haynes Anne-Maree, Liu Zhixin, Delprado Warrick, Shnier Ron, de Reijke Theo M, Lawrentschuk Nathan, Stijns Pascal E F, Yaxley John W, Scheltema Matthijs J, Stricker Phillip D
Garvan Institute of Medical Research and The Kinghorn Cancer Centre, Darlinghurst, Sydney, NSW, Australia; Department of Urology, St. Vincent's Prostate Cancer Research Centre, Darlinghurst, Sydney, NSW, Australia; Department of Radiology and Nuclear Medicine, Amsterdam University Medical Centers (location VUmc), Free University, Amsterdam, The Netherlands.
Garvan Institute of Medical Research and The Kinghorn Cancer Centre, Darlinghurst, Sydney, NSW, Australia; Department of Urology, St. Vincent's Prostate Cancer Research Centre, Darlinghurst, Sydney, NSW, Australia.
Eur Urol Focus. 2022 Nov;8(6):1591-1598. doi: 10.1016/j.euf.2022.04.010. Epub 2022 May 14.
Accurate monitoring following focal treatment of prostate cancer (PCa) is paramount for timely salvage treatment or retreatment.
To evaluate the diagnostic accuracy of multiparametric magnetic resonance imaging (mpMRI) to detect residual PCa in the short-term follow-up of focal treatment with irreversible electroporation (IRE) using transperineal or transrectal template ± targeted biopsies.
DESIGN, SETTING, AND PARTICIPANTS: A retrospective international multicenter study of men with biopsy-proven PCa, treated with focal IRE, and followed by mpMRI (index-test) and template biopsies (reference-test) between February 2013 and January 2021, was conducted.
Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of mpMRI were calculated for in- and outfield residual disease based on two definitions of significant PCa: University College London (UCL) 1-International Society of Urological Pathology (ISUP) ≥3 or ISUP ≥1 with maximum cancer core length (MCCL) ≥6 mm, and UCL2-ISUP ≥2 or ISUP ≥1 with MCCL ≥4 mm.
A total of 303 patients from five focal therapy centers were treated with primary IRE. The final analysis was performed on 217 men (median age 67, median prostate-specific antigen 6.2, 81% ISUP 2/3) who underwent both mpMRI and template biopsies. Multiparametric MRI missed 38/57 (67%) positive biopsy locations (UCL1) in 22 patients. Sensitivity, specificity, PPV, and NPV of mpMRI to detect whole gland residual disease (UCL1) were 43.6% (95% confidence interval [CI]: 28-59), 80.9% (95% CI: 75-86), 33.3% (95% CI: 21-47), and 86.7% (95% CI: 81-91), respectively. Based on UCL2, sensitivity, specificity, PPV, and NPV were 35.8% (95% CI: 25-48), 82.0% (95% CI: 75-88), 47.1% (95% CI: 34-61), and 74.1% (95% CI: 67-80), respectively. Limitations are the retrospective nature and short follow-up.
The diagnostic accuracy of mpMRI to detect residual clinically significant PCa following IRE was low. Follow-up template biopsies should be performed, regardless of mpMRI results.
We investigated the accuracy of magnetic resonance imaging (MRI) to detect residual prostate cancer after treatment with irreversible electroporation. The accuracy of MRI is insufficient, and we emphasize the importance of confirmatory prostate biopsies.
前列腺癌(PCa)局部治疗后的准确监测对于及时进行挽救性治疗或再次治疗至关重要。
评估多参数磁共振成像(mpMRI)在经会阴或经直肠模板±靶向活检的不可逆电穿孔(IRE)局部治疗短期随访中检测残留PCa的诊断准确性。
设计、设置和参与者:进行了一项回顾性国际多中心研究,研究对象为2013年2月至2021年1月间经活检证实患有PCa、接受局部IRE治疗、随后接受mpMRI(索引测试)和模板活检(参考测试)的男性。
基于两种临床显著PCa的定义,计算mpMRI检测场内和场外残留疾病的敏感性、特异性、阳性预测值(PPV)和阴性预测值(NPV):伦敦大学学院(UCL)1-国际泌尿病理学会(ISUP)≥3或ISUP≥1且最大癌芯长度(MCCL)≥6mm,以及UCL2-ISUP≥2或ISUP≥1且MCCL≥4mm。
来自五个聚焦治疗中心的303例患者接受了初次IRE治疗。对217名男性(中位年龄67岁,中位前列腺特异性抗原6.2,81%为ISUP 2/3)进行了最终分析,这些男性同时接受了mpMRI和模板活检。多参数MRI在22例患者中遗漏了38/57(67%)个阳性活检部位(UCL1)。mpMRI检测全腺残留疾病(UCL1)的敏感性、特异性、PPV和NPV分别为43.6%(95%置信区间[CI]:28-59)、80.9%(95%CI:75-86)、33.3%(95%CI:21-47)和86.7%(95%CI:81-91)。基于UCL2,敏感性、特异性、PPV和NPV分别为35.8%(95%CI:25-48)、82.0%(95%CI:75-88)、47.1%(95%CI:34-61)和74.1%(95%CI:67-80)。局限性在于研究的回顾性性质和随访时间短。
mpMRI检测IRE后残留的临床显著PCa的诊断准确性较低。无论mpMRI结果如何,都应进行随访模板活检。
我们研究了磁共振成像(MRI)检测不可逆电穿孔治疗后残留前列腺癌的准确性。MRI的准确性不足,我们强调了确认性前列腺活检的重要性。