Departments of Hematopathology, Division of Pathology and Laboratory Medicine.
Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
Am J Surg Pathol. 2018 May;42(5):569-577. doi: 10.1097/PAS.0000000000000970.
Isocitrate dehydrogenase 1 (IDH1) and IDH2 mutations occur in a variety of myeloid neoplasms. Immunohistochemistry (IHC)-based direct visualization of mutant clones of hematopoietic cells can be useful for rapid diagnostic screening and for monitoring treatment response. In this study, we first evaluated the sensitivity and specificity of the IDH1 p.R132H mutation-specific antibody by IHC. All IDH1 wild type cases (n=11) and IDH1 mutant cases with a non-p.R132H mutation (n=30) were negative by IHC, demonstrating 100% antibody specificity. All the initial diagnostic specimens with IDH1 p.R132H mutation including acute myeloid leukemia (n=30), myelodysplastic syndromes (MDS) (n=10), MDS/myeloproliferative neoplasms (MPN) (n=4), and MPN (n=5) were positive by IHC, demonstrating 100% antibody sensitivity. Both immature and mature myeloid cells showed immunoreactivity. Erythroid precursors, lymphoid cells, endothelial cells, and osteoblasts were consistently negative by IHC. We then evaluated the follow-up specimens with a known IDH1 mutation status including acute myeloid leukemia (n=23), MDS (n=2), MDS/MPN (n=2), and MPN (n=2). Thirty-three IDH1 p.R132H mutant cases were positive by IHC and 12 IDH1 mutation negative cases were negative by IHC. However, IHC reactivity in up to 25% of bone marrow cells was noted in 8 of 20 polymerase chain reaction-negative cases, all from patients with a known history of IDH1 p.R132H mutation indicating sampling error or a sensitivity issue with molecular tests. These data indicate that IHC is a highly specific and sensitive tool to detect IDH1 p.R132H mutation in bone marrow involved by myeloid neoplasms. In addition, IDH1 p.R132H IHC also allows localization and assessment of the maturation stage of the clones carrying the mutation.
异柠檬酸脱氢酶 1(IDH1)和 IDH2 突变发生在多种髓系肿瘤中。基于免疫组织化学(IHC)的造血细胞突变克隆的直接可视化可用于快速诊断筛选和监测治疗反应。在这项研究中,我们首先通过 IHC 评估了 IDH1 p.R132H 突变特异性抗体的敏感性和特异性。所有 IDH1 野生型病例(n=11)和 IDH1 非 p.R132H 突变病例(n=30)均通过 IHC 呈阴性,表明抗体特异性为 100%。所有具有 IDH1 p.R132H 突变的初始诊断标本,包括急性髓系白血病(n=30)、骨髓增生异常综合征(MDS)(n=10)、MDS/骨髓增生性肿瘤(MPN)(n=4)和 MPN(n=5),均通过 IHC 呈阳性,表明抗体敏感性为 100%。幼稚和成熟的髓系细胞均显示免疫反应性。红系前体细胞、淋巴样细胞、内皮细胞和成骨细胞通过 IHC 始终呈阴性。然后,我们评估了具有已知 IDH1 突变状态的随访标本,包括急性髓系白血病(n=23)、MDS(n=2)、MDS/MPN(n=2)和 MPN(n=2)。33 例 IDH1 p.R132H 突变病例通过 IHC 呈阳性,12 例 IDH1 突变阴性病例通过 IHC 呈阴性。然而,在 20 例聚合酶链反应阴性病例中,有 8 例高达 25%的骨髓细胞有免疫反应性,这些病例均来自已知 IDH1 p.R132H 突变病史的患者,表明存在取样误差或分子检测的敏感性问题。这些数据表明,IHC 是一种高度特异和敏感的工具,可用于检测骨髓中涉及的髓系肿瘤中的 IDH1 p.R132H 突变。此外,IDH1 p.R132H IHC 还可以定位和评估携带突变的克隆的成熟阶段。