Norris Joseph M, Simmons Lucy A M, Kanthabalan Abi, Freeman Alex, McCartan Neil, Moore Caroline M, Punwani Shonit, Whitaker Hayley C, Emberton Mark, Ahmed Hashim U
UCL Division of Surgery & Interventional Science, University College London, London, UK.
Department of Urology, University College London Hospitals NHS Foundation Trust, London, UK.
Eur Urol Open Sci. 2021 Jun 15;30:16-24. doi: 10.1016/j.euros.2021.06.003. eCollection 2021 Aug.
Multiparametric magnetic resonance imaging (mpMRI) has improved risk stratification for suspected prostate cancer in patients following prior biopsy. However, not all significant cancers are detected by mpMRI. The PICTURE study provides the ideal opportunity to investigate cancer undetected by mpMRI owing to the use of 5 mm transperineal template mapping (TTPM) biopsy.
To summarise attributes of cancers systematically undetected by mpMRI in patients with prior biopsy.
PICTURE was a paired-cohort confirmatory study in which men requiring repeat biopsy underwent mpMRI followed by TTPM biopsy.
Attributes were compared between cancers detected and undetected by mpMRI at the patient level. Four predefined histopathological thresholds were used as the target condition for TTPM biopsy. Application of prostate-specific antigen density (PSAD) was explored.
When nonsuspicious mpMRI was defined as Likert score 1-2, 2.9% of patients (3/103; 95% confidence interval [CI] 0.6-8.3%) with definition 1 disease (Gleason ≥ 4 + 3 of any length or maximum cancer core length [MCCL] ≥ 6 mm of any grade) had their cancer not detected by mpMRI. This proportion was 6.5% (11/168; 95% CI 3.3-11%) for definition 2 disease (Gleason ≥ 3 + 4 of any length or MCCL ≥ 4 mm of any grade), 4.8% (7/146; 95% CI 2.0-9.6%) for any amount of Gleason ≥ 3 + 4 cancer, and 9.3% (20/215; 95% CI 5.8-14%) for any cancer. Definition 1 cancers undetected by mpMRI had lower overall Gleason score ( = 0.02) and maximum Gleason score ( = 0.01) compared to cancers detected by mpMRI. Prostate cancers undetected by mpMRI had shorter MCCL than cancers detected by mpMRI for every cancer threshold: definition 1, 6 versus 8 mm ( = 0.02); definition 2, 5 versus 6 mm ( = 0.04); any Gleason ≥ 3 + 4, 5 versus 6 mm ( = 0.03); and any cancer, 3 versus 5 mm ( = 0.0009). A theoretical PSAD threshold of 0.15 ng/ml/ml reduced the proportion of patients with undetected disease on nonsuspicious mpMRI to 0% (0/105; 95% CI 0-3.5%) for definition 1, 0.58% (1/171; 95% CI 0.01-3.2%) for definition 2, and 0% (0/146) for any Gleason ≥ 3 + 4.
Few significant cancers are undetected by mpMRI in patients requiring repeat prostate biopsy. Undetected tumours are of lower overall and maximum Gleason grade and shorter cancer length compared to cancers detected by mpMRI.
In patients with a previous prostate biopsy, magnetic resonance imaging (MRI) overlooks few prostate cancers, and these tend to be smaller and less aggressive than cancer that is detected.
多参数磁共振成像(mpMRI)改善了既往活检后疑似前列腺癌患者的风险分层。然而,并非所有显著癌症都能通过mpMRI检测到。PICTURE研究提供了一个理想的机会,可用于研究因采用5毫米经会阴模板映射(TTPM)活检而未被mpMRI检测到的癌症。
总结既往活检患者中未被mpMRI系统检测到的癌症的特征。
设计、设置和参与者:PICTURE是一项配对队列验证性研究,其中需要重复活检的男性先接受mpMRI检查,随后进行TTPM活检。
在患者层面比较了mpMRI检测到和未检测到的癌症之间的特征。四个预定义的组织病理学阈值被用作TTPM活检的目标条件。探索了前列腺特异性抗原密度(PSAD)的应用。
当将非可疑mpMRI定义为李克特评分为1 - 2分时,对于定义1疾病(任何长度的Gleason≥4 + 3或任何分级的最大癌芯长度[MCCL]≥6毫米),2.9%的患者(3/103;95%置信区间[CI] 0.6 - 8.3%)的癌症未被mpMRI检测到。对于定义2疾病(任何长度的Gleason≥3 + 4或任何分级的MCCL≥4毫米),这一比例为6.5%(11/168;95% CI 3.3 - 11%),对于任何量的Gleason≥3 + 4癌症,为4.8%(7/146;95% CI 2.0 - 9.6%),对于任何癌症,为9.3%(20/215;95% CI 5.8 - 14%)。与mpMRI检测到的癌症相比,未被mpMRI检测到的定义1癌症的总体Gleason评分更低(P = 0.02),最大Gleason评分更低(P = 0.01)。对于每个癌症阈值,未被mpMRI检测到的前列腺癌的MCCL比mpMRI检测到的癌症更短:定义1,6毫米对8毫米(P = 0.02);定义2,5毫米对6毫米(P = 0.04);任何Gleason≥3 + 4,5毫米对6毫米(P = 0.03);任何癌症,3毫米对5毫米(P = 0.0009)。理论上PSAD阈值为0.15 ng/ml/ml时,对于定义1,非可疑mpMRI上未检测到疾病的患者比例降至0%(0/105;95% CI 0 - 3.5%),对于定义2,降至0.58%(1/171;95% CI 0.01 - 3.2%),对于任何Gleason≥3 + 4,降至0%(0/146)。
在需要重复前列腺活检的患者中,很少有显著癌症未被mpMRI检测到。与mpMRI检测到的癌症相比,未检测到的肿瘤总体和最大Gleason分级更低,癌长度更短。
在既往有前列腺活检的患者中,磁共振成像(MRI)漏诊的前列腺癌很少,而且这些癌症往往比检测到的癌症更小、侵袭性更低。