IDH突变胶质瘤患者长期生存的决定因素。

IF 3.2 2区 医学 Q2 CLINICAL NEUROLOGY
Sophie Katzendobler, Sebastian Niedermeyer, Jens Blobner, Christoph Trumm, Patrick N Harter, Louisa von Baumgarten, Veit M Stoecklein, Joerg-Christian Tonn, Michael Weller, Niklas Thon, Jonathan Weller
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引用次数: 0

摘要

背景:IDH突变胶质瘤患者的生存期长短不一,可长达数十年。许多研究提供的是无进展生存期而非总生存期,预后因素仍未明确。在此,我们探讨了长期随访患者队列中短期和长期幸存者的特征:这项单中心病例对照研究纳入了在 1998 年至 2023 年间确诊的 86 名患者,他们要么在确诊后 6 年内死亡,要么存活至少 15 年。患者特征和预后因素按短期--分层:回顾性纳入了47例星形细胞瘤患者(55%)和39例少突胶质细胞瘤患者(45%)。幸存者的中位随访时间为 16.6 年(15-28.9 年不等)。数据库关闭时已报告34例死亡病例(40%)。长期生存率与中枢神经系统 WHO 2 级相关(P 结论:T2 肿瘤体积大、造影剂增强与中枢神经系统 WHO 2 级相关:T2肿瘤体积大和对比度增强可能是导致生存期缩短的重要风险因素,而年龄的重要性可能较低。等待和扫描策略可能会使一些星形细胞瘤患者获得良好的长期生存。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determinants of long-term survival in patients with IDH-mutant gliomas.

Background: Survival times of patients with IDH-mutant gliomas are variable and can extend to decades. Many studies provide progression-free rather than overall survival times and prognostic factors remain ill-defined. Here we explored characteristics of short- and long-term survivors within a cohort of patients with extended follow-up.

Methods: This single-center, case-control study included 86 patients diagnosed between 1998 and 2023 who either died within 6 years after diagnosis or survived at least 15 years. Patient characteristics and prognostic factors were stratified by short- (< 6 years) versus long-term (≥ 15 years) survival.

Results: Forty-seven patients (55%) diagnosed with astrocytoma and 39 patients (45%) with oligodendroglioma were included retrospectively. Median follow-up of the survivors was 16.6 years (range 15-28.9). Thirty-four deaths (40%) had been reported at database closure. Long-term survival was associated with CNS WHO grade 2 (p < 0.01), smaller tumor volumes (p = 0.01), lack of contrast enhancement (p < 0.01), wait-and-scan strategies (p < 0.01) and female sex (p = 0.04). In multivariate analyses for oligodendroglioma, larger T2 tumor volumes were associated with shorter survival (HR 1.02; 95% CI 1.01-1.05; p = 0.04). In patients with astrocytoma, lack of contrast enhancement (HR 0.38; 95% CI 0.15-0.94; p = 0.04) and wait-and-scan strategies (HR 5.75; 95% CI 1.66-26.61; p = 0.01) were associated with longer survival.

Conclusion: Large T2 tumor volume and contrast enhancement may be important risk factors for shorter survival, while age might be of lesser importance. Wait-and-scan strategies may yield excellent long-term survival in some patients with astrocytoma.

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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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