Korshunov A, Golanov A
Department of Neuropathology, Neurosurgical NN Burdenko Institute, Moscow, Russia.
J Neurooncol. 2001 Mar;52(1):63-72. doi: 10.1023/a:1010648006319.
Pleomorphic xanthoastrocytomas (PXAs) are characterized as a well-delineated tumor entity with clear peculiarities in clinico-radiological picture, pathological appearance and biological behavior. Usually the PXAs are associated with relatively good prognosis. Nevertheless, up to 35% of patients die following one and more recurrence with or without tumor malignant transformation. Till now, there is no agreement on what histopathological features constitute to objective and reliable signs of PXAs malignancy and clinical outcome. Thirty-four PXAs were subdivided on three subsets: typical (Grade I) - tumors without mitoses per 20 high power fields, proliferating (Grade II) tumors with mitoses but without necroses, and malignant (Grade III) - tumors with elevated mitotic index and necrotic foci. Also, immunohistochemical investigation with various tumor-associated antigens was performed. All PXAs subtypes showed differences in clinical outcomes. There were no recurrences and death among the tumors Grade I. Five out of 14 (36%) Grade II PXAs have recurred and one of them died. All 5 patients with PXAs Grade III have rapidly recurred and four of them died. Immunohistochemical variables, such as Ki-S1, p27/Kip1, vascular endothelial growth factor expression, p53 immunoreactivity and apoptotic index also exhibited significant differences among the three PXAs grades. The progression-free survival was significantly reduced for PXAs grade and presence of mitoses, whereas overall survival was reduced for mitotic index >or= 3 and presence of necroses. No one from immunohistochemical variables reached significant value. In summary, the three-tiered PXAs subdivision proposed by us is carrying some element of rationality but, undoubtedly, requires further prospective studies.
多形性黄色星形细胞瘤(PXAs)的特征是一种界限清楚的肿瘤实体,在临床放射学表现、病理外观和生物学行为方面具有明显的独特性。通常,PXAs的预后相对较好。然而,高达35%的患者在一次或多次复发后死亡,无论是否发生肿瘤恶变。到目前为止,对于哪些组织病理学特征构成PXAs恶性和临床结果的客观可靠指标尚无共识。34例PXAs被分为三个亚组:典型(I级)——每20个高倍视野无有丝分裂的肿瘤;增殖性(II级)——有有丝分裂但无坏死的肿瘤;恶性(III级)——有丝分裂指数升高和坏死灶的肿瘤。此外,还进行了各种肿瘤相关抗原的免疫组化研究。所有PXAs亚型在临床结果上均有差异。I级肿瘤无复发和死亡。14例II级PXAs中有5例(36%)复发,其中1例死亡。所有5例III级PXAs均迅速复发,其中4例死亡。免疫组化变量,如Ki-S1、p27/Kip1、血管内皮生长因子表达、p53免疫反应性和凋亡指数在三个PXAs级别之间也表现出显著差异。PXAs级别和有丝分裂的存在使无进展生存期显著缩短,而有丝分裂指数≥3和坏死的存在使总生存期缩短。免疫组化变量中没有一个达到显著值。总之,我们提出的三层PXAs细分具有一定的合理性,但无疑需要进一步的前瞻性研究。