Differences in the Prognostic Role of Age, Extent of Resection, and Tumor Grade between Astrocytoma IDHmt and Oligodendroglioma: A Single-Center Cohort Study.

IF 10 1区 医学 Q1 ONCOLOGY Clinical Cancer Research Pub Date : 2024-09-03 DOI:10.1158/1078-0432.CCR-24-0901
Thijs van der Vaart, Maarten M J Wijnenga, Karin van Garderen, Hendrikus J Dubbink, Pim J French, Marion Smits, Clemens M F Dirven, Johan M Kros, Arnaud J P E Vincent, Martin J van den Bent
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Abstract

Purpose: IDH-mutant glioma is classified as oligodendroglioma or astrocytoma based on 1p19q-codeletion. Whether prognostic factors are similar between these tumor types is not well understood.

Experimental design: Retrospective cohort study. Molecular characterization was performed with targeted next-generation sequencing. Tumor volumes were calculated using semiautomatic 3D segmentation on all pre- and post-operative MRI scans. Overall survival was assessed with the Cox-proportional hazards model.

Results: A total of 383 patients with newly diagnosed IDH-mutant glioma were followed up for a median of 7.2 years. Grades 3 and 4 patients had significantly lower Karnofsky performance, with tumors having more contrast enhancement. Patients also received more aggressive postsurgery treatment. Postoperative tumor volume is significantly and independently associated with survival (HR, per cm3 1.19; 95% CI, 1.03-1.39) in IDH-mutant glioma. A separate analysis of oligodendroglioma and astrocytoma showed a significant association of postoperative tumor volume in astrocytoma but not in oligodendroglioma. Higher age and histologic tumor grade were associated with worse survival in patients with oligodendroglioma but not with astrocytoma.

Conclusions: Our data support an initial strategy of extensive resection in patients with oligodendroglioma and astrocytoma. Other important prognostic factors differ between these tumor types, urging researchers and clinicians to keep treating these tumors as separate entities.

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星形细胞瘤IDHmt和少突胶质细胞瘤在年龄、切除范围和肿瘤分级方面的预后作用差异:一项单中心队列研究。
目的:IDH突变型胶质瘤根据1p19q码列分为少突胶质瘤和星形细胞瘤。实验设计:回顾性队列研究:实验设计:回顾性队列研究。采用靶向新一代测序技术进行分子特征描述。通过对所有术前和术后磁共振成像扫描进行半自动三维分割计算肿瘤体积。采用Cox比例危险模型评估总生存率:对383名新确诊的IDH突变胶质瘤患者进行了中位7.2年的随访。3级和4级患者的Karnofsky表现明显较低,肿瘤的对比度增强程度更高。患者术后也接受了更积极的治疗。术后肿瘤体积与IDH突变胶质瘤患者的生存率有明显的独立相关性(每立方厘米HR值为1.19,95% CI为1.03 - 1.39)。对少突胶质细胞瘤和星形细胞瘤的单独分析显示,星形细胞瘤的术后肿瘤体积与生存率有显著相关性,而少突胶质细胞瘤则没有。年龄越大、肿瘤组织学分级越高,少突胶质细胞瘤患者的生存率越低,而星形细胞瘤患者的生存率则越低:我们的数据支持对少突胶质细胞瘤和星形细胞瘤患者采取广泛切除的初步策略。这些肿瘤类型的其他重要预后因素也不尽相同,因此研究人员和临床医生应继续将这些肿瘤作为独立的实体进行治疗。
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来源期刊
Clinical Cancer Research
Clinical Cancer Research 医学-肿瘤学
CiteScore
20.10
自引率
1.70%
发文量
1207
审稿时长
2.1 months
期刊介绍: Clinical Cancer Research is a journal focusing on groundbreaking research in cancer, specifically in the areas where the laboratory and the clinic intersect. Our primary interest lies in clinical trials that investigate novel treatments, accompanied by research on pharmacology, molecular alterations, and biomarkers that can predict response or resistance to these treatments. Furthermore, we prioritize laboratory and animal studies that explore new drugs and targeted agents with the potential to advance to clinical trials. We also encourage research on targetable mechanisms of cancer development, progression, and metastasis.
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