Pathology Unit, Department of Woman and Child's Health Sciences and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy; Pathology Unit, Department of Advanced Biomedical Sciences, Federico II University of Naples, Naples, Italy.
Division of Gynaecology and Human Reproduction Physiopathology, Department of Medical and Surgical Sciences (DIMEC), IRCCS Azienda Ospedaliera Univeristaria Di Bologna. S. Orsola Hospital, University of Bologna, Bologna, Italy.
Pathol Res Pract. 2022 Sep;237:154019. doi: 10.1016/j.prp.2022.154019. Epub 2022 Jul 13.
Endometrial clear cell carcinoma (CCC) shows morphological overlap with endometrioid and serous carcinoma. We aimed to assess the accuracy of immunohistochemical diagnostic markers of CCC, i.e. HNF1β, Napsin A and P504S/Alpha-Methylacyl-CoA Racemase (AMACR). A systematic review and meta-analysis was conducted by searching 4 electronic databases from their inception to April 2022 for all studies assessing HNF1β, Napsin A and/or AMACR in endometrial CCC vs endometrioid/serous carcinomas. Diagnostic accuracy was assessed as sensitivity, specificity, positive and negative likelihood ratios (LR+ and LR-), diagnostic odds ratio (DOR) and area under the curve (AUC) on sROC curves. Eleven studies were included. HNF1β positivity (any expression) showed sensitivity= 0.78; specificity= 0.81; LR+ =2.46; LR-= 0.38; DOR= 5.96; AUC= 0.79. Diffuse HNF1β expression showed sensitivity= 0.53; specificity= 0.95; LR+ =9.68; LR-= 0.51; DOR= 18.02; AUC= 0.40. Napsin A positivity (any expression) showed sensitivity= 0.76; specificity= 0.97; LR+ =18.79; LR-= 0.27; DOR= 73.31; AUC= 0.81. Diffuse Napsin A expression showed sensitivity= 0.52; specificity= 0.99; LR+ =14.50; LR-= 0.55; DOR= 24.93; AUC= 0.98. AMACR positivity (any expression) showed sensitivity= 0.76; specificity= 0.86; LR+ =4.86; LR-= 0.30; DOR= 13.56; AUC was not assessable due to the presence of only 2 studies. In conclusion, HNF1β, Napsin A and AMACR show moderate accuracy in identifying endometrial CCC. Considering only a diffuse expression of these markers as positive leads to high specificity but low sensitivity. In particular, Napsin A appears as the most specific marker of endometrial CCC.
子宫内膜透明细胞癌(CCC)在形态上与子宫内膜样癌和浆液性癌重叠。我们旨在评估 HNF1β、Napsin A 和 P504S/Alpha-Methylacyl-CoA Racemase(AMACR)等 CCC 的免疫组织化学诊断标志物的准确性。通过从开始到 2022 年 4 月在 4 个电子数据库中搜索所有评估子宫内膜 CCC 与子宫内膜样/浆液性癌中 HNF1β、Napsin A 和/或 AMACR 的研究,进行了系统评价和荟萃分析。诊断准确性评估为灵敏度、特异性、阳性和阴性似然比(LR+和 LR-)、诊断比值比(DOR)和 sROC 曲线下面积(AUC)。纳入了 11 项研究。HNF1β 阳性(任何表达)的灵敏度=0.78;特异性=0.81;LR+=2.46;LR-=0.38;DOR=5.96;AUC=0.79。弥漫性 HNF1β 表达的灵敏度=0.53;特异性=0.95;LR+=9.68;LR-=0.51;DOR=18.02;AUC=0.40。Napsin A 阳性(任何表达)的灵敏度=0.76;特异性=0.97;LR+=18.79;LR-=0.27;DOR=73.31;AUC=0.81。弥漫性 Napsin A 表达的灵敏度=0.52;特异性=0.99;LR+=14.50;LR-=0.55;DOR=24.93;AUC=0.98。AMACR 阳性(任何表达)的灵敏度=0.76;特异性=0.86;LR+=4.86;LR-=0.30;DOR=13.56;由于仅存在 2 项研究,AUC 不可评估。总之,HNF1β、Napsin A 和 AMACR 在识别子宫内膜 CCC 方面具有中等准确性。仅考虑这些标志物的弥漫性表达为阳性会导致高特异性和低灵敏度。特别是,Napsin A 似乎是子宫内膜 CCC 最特异的标志物。