Clinical and neuropathological criteria for distinguishing between IDH-mutant astrocytomas of WHO grade 2 and 3.

IF 3.1 2区 医学 Q2 CLINICAL NEUROLOGY
Journal of Neuro-Oncology Pub Date : 2025-11-01 Epub Date: 2025-07-23 DOI:10.1007/s11060-025-05173-z
Jens Blobner, Viktoria Ruf, Jonathan Weller, Nico Teske, Robert Forbrig, Niklas Thon, Nathalie L Albert, Louisa von Baumgarten, Stephan Schoenecker, Joerg-Christian Tonn, Florian Ringel, Patrick N Harter, Philipp Karschnia
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Abstract

Background: The 2021 WHO classification of CNS tumors allows flexibility in the grading of IDH-mutant astrocytic gliomas, leading to some ambiguity. Following the approval of vorasidenib for WHO grade 2 astrocytomas and oligodendrogliomas based on the positive Phase III INDIGO trial, identifying prognostic criteria to differentiate between grade 2 and grade 3 tumors has become increasingly important.

Methods: We retrospectively searched our institutional database for patients meeting the diagnostic criteria for IDH-mutant astrocytomas (grade 2 and 3) according to the WHO 2021 classification. Clinical, radiological and molecular data were collected; outcome was compared using log-rank analysis and prognostic markers were subsequently forwarded in a multivariate model.

Results: We identified 91 patients with IDH-mutant astrocytomas with available neuropathological and clinical data, including 61 WHO grade 2 (67.0%) and 30 WHO grade 3 (33.0%) tumors. At a median follow-up of 89 months, median progression-free survival was 67 months for WHO grade 2 and 53 months for WHO grade 3 tumors. Median overall survival was 216 months for WHO grade 3 tumors, while it was not reached for WHO grade 2 tumors. Univariate analysis showed that higher WHO grade, increased mitotic count, elevated Ki67 indices and preoperative contrast enhancement were associated with poorer outcomes; however, only contrast enhancement retained prognostic significance on multivariate analysis (p = 0.03 for overall survival, p = 0.02 for progression-free survival).

Conclusion: While our findings await confirmation in larger prospective cohorts, neuropathological grading criteria might need to be accompanied by clinical information including contrast enhancement to prognostically distinguish grade 2 from grade 3 tumors.

Abstract Image

Abstract Image

区分WHO 2级和3级idh突变星形细胞瘤的临床和神经病理学标准。
背景:2021年WHO对中枢神经系统肿瘤的分类允许对idh突变型星形细胞胶质瘤的分级具有灵活性,从而导致一些模糊性。基于INDIGO III期阳性试验,vorasidenib被批准用于WHO 2级星形细胞瘤和少突胶质细胞瘤,鉴别2级和3级肿瘤的预后标准变得越来越重要。方法:根据WHO 2021分类,我们回顾性检索了符合idh突变星形细胞瘤(2级和3级)诊断标准的机构数据库。收集临床、放射学和分子资料;结果采用对数秩分析进行比较,预后指标随后在多变量模型中转发。结果:我们确定了91例具有可用神经病理和临床资料的idh突变星形细胞瘤患者,其中61例WHO分级2级(67.0%)和30例WHO分级3级(33.0%)肿瘤。在中位随访89个月时,WHO 2级肿瘤的中位无进展生存期为67个月,WHO 3级肿瘤的中位无进展生存期为53个月。WHO 3级肿瘤的中位总生存期为216个月,而WHO 2级肿瘤的中位总生存期未达到。单因素分析显示,较高的WHO分级、有丝分裂计数增加、Ki67指数升高和术前对比增强与较差的预后相关;然而,在多变量分析中,只有对比增强保留了预后意义(总生存期p = 0.03,无进展生存期p = 0.02)。结论:虽然我们的研究结果有待更大的前瞻性队列的证实,但神经病理分级标准可能需要伴随着临床信息,包括对比增强,以在预后上区分2级和3级肿瘤。
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来源期刊
Journal of Neuro-Oncology
Journal of Neuro-Oncology 医学-临床神经学
CiteScore
6.60
自引率
7.70%
发文量
277
审稿时长
3.3 months
期刊介绍: The Journal of Neuro-Oncology is a multi-disciplinary journal encompassing basic, applied, and clinical investigations in all research areas as they relate to cancer and the central nervous system. It provides a single forum for communication among neurologists, neurosurgeons, radiotherapists, medical oncologists, neuropathologists, neurodiagnosticians, and laboratory-based oncologists conducting relevant research. The Journal of Neuro-Oncology does not seek to isolate the field, but rather to focus the efforts of many disciplines in one publication through a format which pulls together these diverse interests. More than any other field of oncology, cancer of the central nervous system requires multi-disciplinary approaches. To alleviate having to scan dozens of journals of cell biology, pathology, laboratory and clinical endeavours, JNO is a periodical in which current, high-quality, relevant research in all aspects of neuro-oncology may be found.
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