Department of Pathology, University of Michigan Medical School, 2800 Plymouth Road, Building 35, Ann Arbor, MI, USA.
Department of Hematology/Oncology, University of Michigan, Ann Arbor, MI, USA.
Med Oncol. 2021 Feb 14;38(3):26. doi: 10.1007/s12032-021-01473-2.
Neuroendocrine transdifferentiation of high-grade prostate cancer (PCA-NT) comprises a morphologic and immunophenotypic transition from conventional adenocarcinoma towards high-grade neuroendocrine/small cell carcinoma. This phenomenon is frequently observed post androgen deprivation and/or radiotherapy, but de novo instances are increasingly recognized. Herein, we report a series of de novo PCA-NT focusing on characteristic morphologic, immunophenotypic and clinical features. Treatment naïve PCA-NT were identified. IHC for PSA, NKX3.1, Chromogranin, Synaptophysin, Cyclin D1, RB and Ki67 were performed. Radiology, treatment and follow-up data were reviewed. Sixteen patients were included. Apart from focal areas of high-grade prostate cancer with acinar features (reminiscent of Grade Group 5 disease), extensive areas with sheets of cells with deep amphophilic/basophilic cytoplasm, enlarged, hyperchromatic nuclei with granular chromatin and inconspicuous to prominent nucleoli with high mitotic activity were identified. Immunohistochemistry showed patchy NKX3.1, patchy PSA, variable Synaptophysin and Chromogranin; RB and CyclinD1 showed loss of expression. Ki67 showed high proliferative index, in most cases. Adverse radiologic findings and metastases were documented in most cases. Two patients died of disease. De novo PCA-NT exhibits high-grade nuclei, high mitotic activity, reduced PSA expression with high Ki67 and functional inactivation of RB1 pathway, suggesting transition from androgen-driven to proliferation-driven phenotype. Most cases presented at advanced stage with adverse radiological findings, metastasis at time of diagnosis, and high mortality. In light of their prognostic and therapeutic implications, pathologists may need to maintain a sensitive threshold for performing immunostains-in particular, Ki67 and CyclinD1-when presented with such cases in their day to day clinical practice.
神经内分泌前列腺癌(PCA-NT)的转化包括从常规腺癌向高级别神经内分泌/小细胞癌的形态和免疫表型转变。这种现象在雄激素剥夺和/或放射治疗后经常观察到,但越来越多的是新出现的病例。在此,我们报告了一系列新出现的 PCA-NT,重点关注其特征性的形态、免疫表型和临床特征。我们鉴定了未经治疗的 PCA-NT。进行了 PSA、NKX3.1、嗜铬粒蛋白、突触素、Cyclin D1、RB 和 Ki67 的免疫组化染色。回顾了影像学、治疗和随访数据。纳入了 16 名患者。除了具有腺泡特征的局灶性高级别前列腺癌(类似于 5 级疾病)外,还广泛存在大片细胞呈片状排列,细胞质深嗜碱性/嗜酸性,细胞核增大、深染,染色质颗粒状,核仁不明显至明显,有高有丝分裂活性。免疫组化显示 NKX3.1 呈斑片状、PSA 呈斑片状、突触素和嗜铬粒蛋白呈可变表达;RB 和 CyclinD1 显示表达缺失。Ki67 显示高增殖指数,大多数情况下。大多数病例均有不良的影像学发现和转移。两名患者死于疾病。新出现的 PCA-NT 表现为高级别核、高有丝分裂活性、PSA 表达减少,Ki67 表达高,RB1 通路功能失活,提示从雄激素驱动型向增殖驱动型表型的转变。大多数病例在晚期出现,影像学表现不良,诊断时出现转移,死亡率高。鉴于其预后和治疗意义,病理学家在日常临床实践中遇到此类病例时,可能需要保持对进行免疫组化染色的敏感阈值,特别是 Ki67 和 CyclinD1。