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成年患者中枢神经系统WHO 2级少突胶质细胞瘤的长期预后:单机构经验

Long-term outcomes of CNS WHO grade 2 oligodendroglioma in adult patients: a single-institution experience.

作者信息

Byeon Yukyeng, Lee Chaejin, Jeon Juhee, Kim Gung Ju, Chong Sangjoon, Kim Young-Hoon, Cho Young Hyun, Hong Seok Ho, Hong Chang-Ki, Kim Jeong Hoon, Song Sang Woo

机构信息

Department of Neurological Surgery, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea.

Department of Neurosurgery, Kyungpook National University Hospital, Daegu, 41944, South Korea.

出版信息

Discov Oncol. 2024 Jul 6;15(1):268. doi: 10.1007/s12672-024-01136-4.

Abstract

PURPOSE

Oligodendrogliomas (ODGs) are a subtype of diffuse lower-grade gliomas with overall survival of > 10 years. This study aims to analyze long-term outcomes and identify prognostic factors in patients with WHO grade 2 ODG.

METHODS

We retrospectively reviewed 138 adult patients diagnosed with 1p/19q co-deleted ODG who underwent surgical resection or biopsy between 1994 and 2021, analyzing clinical data, treatment details, and outcomes. Progression-free survival (PFS) and overall survival (OS) were evaluated using Kaplan-Meier analysis. Univariate and multivariate Cox regression analyses were utilized to identify significant prognostic factors.

RESULTS

In the gross total resection (GTR) group, 63 (45.7%) underwent observation and 5 (3.6%) received postoperative treatment; in the non-GTR group, 37 (26.8%) were observed and 33 (23.9%) received postoperative treatment. The median PFS and OS were 6.8 and 18.4 years, respectively. Between adjuvant treatment and observation, there was no significant difference in PFS or OS. However, GTR or STR with less than 10% residual tumor exhibited significantly better PFS and OS compared to PR or biopsy (p = 0.022 and 0.032, respectively). Multivariate analysis revealed that contrast enhancement on MRI was associated with worse PFS (HR = 2.36, p < 0.001) and OS (HR = 5.89, p = 0.001). And the presence of seizures at presentation was associated with improved OS (HR = 0.28, p = 0.006).

CONCLUSION

This study underscores favorable long-term outcomes for patients with 1p/19q co-deleted ODG WHO grade 2. Our findings indicate that the EOR plays a crucial role as a significant prognostic factor in enhancing PFS and OS outcomes in WHO grade 2 ODG.

摘要

目的

少突胶质细胞瘤(ODG)是弥漫性低级别胶质瘤的一种亚型,总体生存期超过10年。本研究旨在分析世界卫生组织(WHO)2级ODG患者的长期预后并确定预后因素。

方法

我们回顾性分析了1994年至2021年间138例诊断为1p/19q共缺失ODG且接受手术切除或活检的成年患者,分析临床资料、治疗细节和预后。采用Kaplan-Meier分析评估无进展生存期(PFS)和总生存期(OS)。运用单因素和多因素Cox回归分析确定显著的预后因素。

结果

在全切除(GTR)组中,63例(45.7%)接受观察,5例(3.6%)接受术后治疗;在非GTR组中,37例(26.8%)接受观察,33例(23.9%)接受术后治疗。PFS和OS的中位数分别为6.8年和18.4年。辅助治疗和观察之间,PFS或OS无显著差异。然而,与部分切除(PR)或活检相比,GTR或残留肿瘤小于10%的次全切除(STR)的PFS和OS显著更好(分别为p = 0.022和0.032)。多因素分析显示,MRI上的强化与较差的PFS(风险比[HR] = 2.36,p < 0.001)和OS(HR = 5.89,p = 0.001)相关。并且发病时存在癫痫与改善的OS相关(HR = 0.28,p = 0.006)。

结论

本研究强调了WHO 2级1p/19q共缺失ODG患者良好的长期预后。我们的研究结果表明,切除范围(EOR)作为一个重要的预后因素,在提高WHO 2级ODG的PFS和OS结局方面起着关键作用。

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