Li Eric V, Busza Anna M, Siddiqui Mohammad R, Aguiar Jonathan A, Keeter Mary-Kate, Neill Clayton, Kumar Sai K, Mi Xinlei, Schaeffer Edward M, Patel Hiten D, Ross Ashley E
Department of Urology, Northwestern University, Feinberg School of Medicine, Chicago, IL, 60611, USA.
Department of Preventive Medicine-Division of Biostatistics, Northwestern University, Feinberg School of Medicine, Chicago, IL, 60611, USA.
Prostate Cancer Prostatic Dis. 2024 Jun 10. doi: 10.1038/s41391-024-00853-9.
Multiparametric prostate MRI (mpMRI) is being increasingly adopted for work-up of prostate cancer. For patients selected to omit biopsy, we identified factors associated with repeat MRI, eventual prostate biopsy, and subsequent detection of clinically significant prostate cancer (csPCa, Grade Group ≥2).
We identified biopsy-naïve men presenting with PSA 2-20 ng/mL (March 2018-June 2021) undergoing initial mpMRI with PIRADS 1-3 lesions who were not selected for biopsy with ≥6 months follow-up. We examined factors associated with repeat mpMRI, progression to biopsy, and subsequent detection of csPCa with univariable and multivariable logistic regression.
Of 1494 men, 31% (463/1494) did not pursue biopsy. PSA density (PSAD) ≤ 0.1, prostate health index (PHI) < 55, and PIRADS 1-2 were associated with omission of prostate biopsy. csPCa diagnosis-free survival was 97.6% (326/334) with median follow up of 23.1 months (IQR 15.1-34.6 months). Black race, PSA, PHI, PSA density, and PSA and PHI velocity were significant predictors of undergoing repeat mpMRI (15.6%, 52/334) and subsequent biopsy (8.4%, 28/334). 8 men were subsequently diagnosed with csPCa (N = 7 on prostate biopsy; N = 1 incidentally on holmium enucleation of prostate). All patients diagnosed with csPCa had PIRADS 4-5 on repeat mpMRI.
The subsequent detection rate of csPCa among patients not initially biopsied after mpMRI was low at 2.4%. Decisions to omit biopsy after initial reassuring PHI, PSAD, and mpMRI appear safe with subsequent reassuring serum biomarkers and for cause mpMRI during follow-up.
多参数前列腺磁共振成像(mpMRI)在前列腺癌检查中的应用越来越广泛。对于选择不进行活检的患者,我们确定了与重复MRI、最终前列腺活检以及随后检测到临床意义重大的前列腺癌(csPCa,分级组≥2)相关的因素。
我们确定了2018年3月至2021年6月期间出现前列腺特异性抗原(PSA)为2 - 20 ng/mL且未接受过活检的男性,他们接受了初次mpMRI检查,结果为前列腺影像报告和数据系统(PIRADS)1 - 3级病变,且未被选择进行活检,并进行了至少6个月的随访。我们通过单变量和多变量逻辑回归分析了与重复mpMRI、进展为活检以及随后检测到csPCa相关的因素。
在1494名男性中,31%(463/1494)未进行活检。PSA密度(PSAD)≤0.1、前列腺健康指数(PHI)<55以及PIRADS 1 - 2与未进行前列腺活检相关。无csPCa诊断的生存率为97.6%(326/334),中位随访时间为23.1个月(四分位间距15.1 - 34.6个月)。黑人种族、PSA、PHI、PSA密度以及PSA和PHI变化率是进行重复mpMRI(15.6%,52/334)和随后活检(8.4%,28/334)的重要预测因素。8名男性随后被诊断为csPCa(7名通过前列腺活检确诊;1名在钬激光前列腺剜除术中偶然发现)。所有被诊断为csPCa的患者在重复mpMRI检查中结果为PIRADS 4 - 5级。
mpMRI后最初未进行活检的患者中,csPCa的后续检出率较低,为2.4%。在初次PHI、PSAD和mpMRI结果令人放心后决定不进行活检,在后续血清生物标志物令人放心以及随访期间因其他原因进行mpMRI检查时,似乎是安全的。