Hacisalihoglu Payam, Kucukodaci Zafer, Gundogdu Gokcen, Bilgic Bilge
Yeni Yuzyil University, Medical Faculty, Gaziosmanpasa Hospital, Department of Pathology, Istanbul, Turkey.
Turk Neurosurg. 2017;27(5):682-689. doi: 10.5137/1019-5149.JTN.16832-15.1.
To observe the correlation between 1p/19q codeletion, isocytrate dehydrogenase-1 (IDH1) mutation and p53 protein overexpression and their prognostic value in Turkish anaplastic oligodendroglioma patients who were treated with adjuvant radiotherapy and temozolomide chemotherapy.
We retrospectively evaluated 41 patients who were diagnosed as anaplastic oligodendroglioma. Thirty-five patients received standard radiotherapy. Twenty-six patients received standard temozolomide chemoterapy concurrent to radiotherapy.
Chromosome 1p/19q codeletion was observed in 19 of 41 patients (46%) via Fluorescent In Situ Hybridisation (FISH) technique. Twenty-six patients (63%) showed positive immunoreaction with anti-IDH1 antibody. Six patients (15%) showed positive immunoreaction with anti-p53 antibody. A statistically significant correlation was determined between chromosome 1p/19q codeletion and IDH1 mutation (p < 0.0001). The patients who had tumors with chromosome 1p/19q codeletion and p53 overexpression were mutually exclusive. The mean estimated Progression Free Survival (PFS) of the patients who had tumors with chromosome 1p/19q codeletion and/or IDH1 mutation was determined to be significantly longer than that of the patients without these genetic changes, regardless of the treatment modality (p=0.006, p=0.004). PFS of the patients who received adjuvant chemotherapy and whose tumors had chromosome 1p/19q codeletion or IDH1 mutation was significantly longer than that of the patients without these genetic changes (p=0.001, p < 0.0001).
Chromosome 1p/19q codeletion and/or IDH1 mutation are favorable prognostic factors in anaplastic oligodendroglioma patients, in terms of PFS.
观察1p/19q共缺失、异柠檬酸脱氢酶-1(IDH1)突变与p53蛋白过表达之间的相关性及其在接受辅助放疗和替莫唑胺化疗的土耳其间变性少突胶质细胞瘤患者中的预后价值。
我们回顾性评估了41例被诊断为间变性少突胶质细胞瘤的患者。35例患者接受了标准放疗。26例患者在放疗的同时接受了标准替莫唑胺化疗。
通过荧光原位杂交(FISH)技术在41例患者中的19例(46%)观察到染色体1p/19q共缺失。26例患者(63%)抗IDH1抗体免疫反应呈阳性。6例患者(15%)抗p53抗体免疫反应呈阳性。确定染色体1p/19q共缺失与IDH1突变之间存在统计学显著相关性(p < 0.0001)。染色体1p/19q共缺失且p53过表达的肿瘤患者相互排斥。无论治疗方式如何,染色体1p/19q共缺失和/或IDH1突变的肿瘤患者的平均无进展生存期(PFS)被确定显著长于无这些基因改变的患者(p = 0.006,p = 0.004)。接受辅助化疗且肿瘤有染色体1p/19q共缺失或IDH1突变的患者的PFS显著长于无这些基因改变的患者(p = 0.001,p < 0.0001)。
就PFS而言,染色体1p/19q共缺失和/或IDH1突变是间变性少突胶质细胞瘤患者的有利预后因素。