University School and Cleveland Clinic Department of Anatomic Pathology, USA.
University School and Cleveland Clinic Department of Anatomic Pathology, USA.
Ann Diagn Pathol. 2020 Dec;49:151653. doi: 10.1016/j.anndiagpath.2020.151653. Epub 2020 Oct 25.
In 2016, the World Health Organization recommended that isocitrate dehydrogenase (IDH) mutation status be included in the classification of diffuse astrocytic gliomas. IDH mutations are part of the current definition of oligodendrogliomas and are predictive of a better outcome in diffuse astrocytic gliomas. A few studies, examining the role of routine IDH testing in older patients, came to differing conclusions and made differing recommendations regarding a routine IDH testing algorithm with respect to patient age. The purpose of this study was to examine IDH mutations in a series of diffuse astrocytic gliomas [N = 381; 53 diffuse astrocytomas (WHO grade II), 66 anaplastic astrocytomas (WHO grade III) and 262 glioblastomas (WHO grade IV)], paying particular attention to age of patient and any relationship between age and IDH status. IDH status was evaluated by immunohistochemistry with IDH-1 (R132H) antibody and if negative staining was noted, followup polymerase chain reaction (PCR) testing assessing for IDH-1 and IDH-2 mutations was performed. Overall, IDH mutations were discovered in 50.1% of grade II tumors, 54.4% of grade III tumors and 15.1% of grade IV tumors. Of tumors studied, 224 tumors (58.8%) arose in patients 55 years or older. Higher rates of IDH mutations were observed in the patient group less than 55 years of age versus those 55 years or older. By PCR testing in patients 55 years or older, non IDH-1 (R132H) mutations were noted in 0/4 grade II tumors, 3/11 grade III tumors and 26/37 grade IV tumors. The results of this study suggest that although IDH mutations in diffuse astrocytic gliomas are more frequently encountered in patients less than 55 years of age, a significant subset of older patients have mutations that would not be discovered on routine immunohistochemistry and therefore, followup PCR testing is recommended for all patients whose tumors are negative by immunohistochemistry.
2016 年,世界卫生组织建议将异柠檬酸脱氢酶(IDH)突变状态纳入弥漫性星形细胞瘤的分类。IDH 突变是目前少突胶质细胞瘤定义的一部分,并可预测弥漫性星形细胞瘤的更好预后。一些研究检查了常规 IDH 检测在老年患者中的作用,得出了不同的结论,并就患者年龄的常规 IDH 检测算法提出了不同的建议。本研究的目的是检查一系列弥漫性星形细胞瘤中的 IDH 突变[N=381;53 例弥漫性星形细胞瘤(WHO 二级),66 例间变性星形细胞瘤(WHO 三级)和 262 例胶质母细胞瘤(WHO 四级)],特别注意患者年龄以及年龄与 IDH 状态之间的任何关系。IDH 状态通过 IDH-1(R132H)抗体的免疫组织化学评估,如果未发现阴性染色,则进行后续聚合酶链反应(PCR)检测以评估 IDH-1 和 IDH-2 突变。总体而言,二级肿瘤中发现 IDH 突变占 50.1%,三级肿瘤占 54.4%,四级肿瘤占 15.1%。在所研究的肿瘤中,224 个肿瘤(58.8%)发生在 55 岁或以上的患者中。年龄小于 55 岁的患者中 IDH 突变率高于年龄大于 55 岁的患者。在年龄大于 55 岁的患者中,通过 PCR 检测发现非 IDH-1(R132H)突变分别见于 0/4 例二级肿瘤、3/11 例三级肿瘤和 26/37 例四级肿瘤。本研究结果表明,尽管 IDH 突变在年龄小于 55 岁的弥漫性星形细胞瘤患者中更为常见,但相当一部分老年患者存在免疫组织化学无法发现的突变,因此建议对所有免疫组织化学阴性的患者进行后续 PCR 检测。