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四期高危神经母细胞瘤:分子、组织学和免疫组织化学特征以及 MYCN 蛋白过表达的 2 种不同模式的存在——来自儿童肿瘤协作组的报告。

Stage 4S Neuroblastoma: Molecular, Histologic, and Immunohistochemical Characteristics and Presence of 2 Distinct Patterns of MYCN Protein Overexpression-A Report From the Children's Oncology Group.

机构信息

Department of Diagnostic Pathology, Graduate School of Medicine, Chiba University, Chiba, Japan.

Departments of Pathology.

出版信息

Am J Surg Pathol. 2021 Aug 1;45(8):1075-1081. doi: 10.1097/PAS.0000000000001647.

Abstract

Stage 4S neuroblastoma (4SNB) is associated with spontaneous tumor regression and an excellent prognosis. However, a small group of the patients have a poor prognosis. One hundred eighty-five stage 4SNB cases filed at the Children's Oncology Group Neuroblastoma Pathology Reference Laboratory were studied. MYCN oncogene status [non-amplified (NA) vs. Amplified (A)] determined by fluorescence in situ hybridization, MYC-family (MYCN/MYC) protein expression [no-overexpression(-)/(+/-) vs. overexpression(+)] by immunohistochemistry and histopathology by International Neuroblastoma Pathology Classification [Favorable Histology (FH) vs. Unfavorable Histology (UH)] with particular attention to nucleolar hypertrophy [NH(-) vs. (+)] were assessed with patient survival. One hundred forty-seven (79.5%) tumors were MYCN-NA, FH, MYC-family protein(-)/(+/-), and NH(-) with a good prognosis [88.5±3.1% 3-y event-free survival (EFS); 94.1±2.3% 3-y overall survival (OS)]. Among MYCN-NA tumors, 11 demonstrated MYCN protein(+) with a moderate and uniform (M/U) staining pattern: they were FH(10/11), NH(-), 1 showed MYC protein(+) simultaneously, and all patients are alive. Also found were 5 MYC protein(+) and MYCN(-)/(+/-) tumors; they were FH without NH (4/5), and all patients are alive. Among MYCN-A tumors, 18 had MYCN protein(+) with a strong and heterogeneous (S/H) staining pattern, 9 had UH (44.4±23.4% EFS/OS) and 9 had FH (68.6±19.2% EFS/OS), and 15 showed NH(+). Two tumors had MYCN protein(-)/(+/-) despite MYCN-A; both were FH and NH(-), and 1 patient died. S/H staining pattern of MYCN protein overexpression by immunohistochemistry was associated with MYCN amplification, NH(+) and a poor prognosis. In contrast, the M/U staining pattern was associated with MYCN nonamplification and NH(-), and had no adverse prognostic effects for the stage 4SNB patients.

摘要

4S 期神经母细胞瘤(4SNB)与自发性肿瘤消退和极好的预后相关。然而,一小部分患者预后较差。研究了儿童肿瘤组神经母细胞瘤病理参考实验室存档的 185 例 4S 期神经母细胞瘤病例。通过荧光原位杂交确定 MYCN 癌基因状态[非扩增(NA)与扩增(A)],通过免疫组织化学确定 MYC 家族(MYCN/MYC)蛋白表达[无过度表达(-)/(+/)与过度表达(+)],并通过国际神经母细胞瘤病理分类进行组织病理学评估[良好组织学(FH)与不良组织学(UH)],特别注意核仁肥大[NH(-)与(+)],并评估患者的生存情况。147 例(79.5%)肿瘤为 MYCN-NA、FH、MYC 家族蛋白(-)/(+/)和 NH(-),预后良好[88.5±3.1%3 年无事件生存率(EFS);94.1±2.3%3 年总生存率(OS)]。在 MYCN-NA 肿瘤中,有 11 例 MYCN 蛋白阳性,且呈均匀(M/U)染色模式:均为 FH(10/11)、NH(-),1 例同时显示 MYC 蛋白阳性,所有患者均存活。还发现 5 例 MYC 蛋白阳性且 MYCN-/-/(+/)肿瘤;均无 NH(4/5),所有患者均存活。在 MYCN-A 肿瘤中,有 18 例 MYCN 蛋白阳性,且呈强异质性(S/H)染色模式,9 例为 UH(44.4±23.4%EFS/OS),9 例为 FH(68.6±19.2%EFS/OS),15 例为 NH(+)。有 2 例 MYCN 蛋白阴性(-)/(+/),尽管 MYCN-A 阳性;均为 FH 和 NH(-),1 例患者死亡。免疫组织化学检测到的 MYCN 蛋白过表达的 S/H 染色模式与 MYCN 扩增、NH(+)和不良预后相关。相比之下,M/U 染色模式与 MYCN 非扩增和 NH(-)相关,对 4S 期神经母细胞瘤患者没有不利的预后影响。

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