低级别脊髓星形细胞瘤的最佳治疗策略:日本神经脊髓协会的回顾性多中心分析。

IF 2.9 2区 医学 Q2 CLINICAL NEUROLOGY Journal of neurosurgery. Spine Pub Date : 2024-09-20 DOI:10.3171/2024.5.SPINE24457
Seiji Shigekawa, Akihiro Inoue, Toshiki Endo, Jun Muto, Tomoo Inoue, Ryo Kanematsu, Takafumi Mitsuhara, Daisuke Umebayashi, Masaki Mizuno, Kazutoshi Hida, Takeharu Kunieda
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引用次数: 0

摘要

目的:原发性脊髓胶质瘤非常罕见,其中星形细胞瘤(世卫组织 II 级)更为罕见。因此,最佳治疗策略仍不明确。作者在日本神经脊柱学会(NSJ)的领导下开展了一项多中心研究,分析治疗政策和结果。目的是介绍脊髓星形细胞瘤的最佳治疗方法,并找出预示更好疗效的因素:在隶属于 NSJ 的 58 个中心接受手术治疗的 1033 例脊髓髓内肿瘤患者中,有 57 例患者被诊断为弥漫性星形细胞瘤(WHO II 级),并被纳入本研究。在这 57 名患者中,作者分析了治疗方法、疗效和通过 MIB-1 染色指数(SI)评估的肿瘤增殖率,并确定了脊髓星形细胞瘤(II 级)的最佳治疗方法。此外,作者还寻找了预测更好治疗效果的因素:脊髓星形细胞瘤的治疗包括三种方法:30例患者单纯手术,13例患者辅助放疗,13例患者辅助化放疗。生存率分析中排除了一名未接受手术的患者。与辅助化学放疗相比,单纯手术治疗或手术加放疗的总生存期和无进展生存期明显更长。放疗患者的MIB-1 SI高于单纯手术患者。肿瘤切除范围往往与较长的生存期相关。与此相反,术后神经功能恶化则呈反序。在全部病例和复发病例中,辅助化放疗与最短的生存期相关。MIB-1 SI的最佳临界值小于4.0%,可预测单纯手术治疗的较长生存期:脊髓星形细胞瘤的最佳治疗方法是在不影响神经功能的情况下最大限度地切除肿瘤。结论:脊髓星形细胞瘤的最佳治疗方法是在不影响神经功能的情况下最大限度地切除肿瘤。当 MIB-1 SI 小于 4.0% 的患者仍有部分肿瘤残留时,最佳治疗方法是静观其变。如果 MIB-1 SI 高于 4.0%,建议进行局部放疗。不建议在治疗 II 级脊髓星形细胞瘤时采用辅助化疗。
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Optimal treatment strategy for low-grade spinal cord astrocytoma: a retrospective, multicenter analysis by the Neurospinal Society of Japan.

Objective: Primary spinal cord gliomas are rare, and among these astrocytomas (WHO grade II) are much rarer. The optimal treatment strategy thus remains unclear. The authors conducted a multicenter study led by the Neurospinal Society of Japan (NSJ) to analyze treatment policies and outcomes. The aim was to present optimal treatment methods for spinal cord astrocytoma and to identify predictors of better outcomes.

Methods: Among 1033 consecutive cases of spinal cord intramedullary tumors treated surgically at 58 centers affiliated with the NSJ, 57 patients were diagnosed with diffuse astrocytoma (WHO grade II) and were enrolled in the present study. Among these 57 patients, treatment methods, outcomes, and tumor proliferation rate as evaluated by the MIB-1 staining index (SI) were analyzed, and the optimal treatment method for spinal cord astrocytomas (grade II) was determined. In addition, the authors searched for factors predicting better treatment outcomes.

Results: Treatment for spinal cord astrocytoma comprised three methods: surgery alone in 30 patients, adjuvant radiation therapy in 13 patients, and adjuvant chemoradiotherapy in 13 patients. One patient who did not undergo surgery was excluded from survival analysis. Treatment with surgery alone or surgery with radiotherapy was associated with significantly longer overall and progression-free survivals than that with adjuvant chemoradiotherapy. Patients treated with radiation therapy had a higher MIB-1 SI than those treated with surgery alone. The extent of tumor resection tended to correlate with longer survival. In contrast, postoperative neurological worsening showed the inverse order. Adjuvant chemoradiotherapy was associated with the shortest survival in both total cases and recurrent cases. The optimal cutoff value of MIB-1 SI for predicting longer survival by surgery alone was less than 4.0%.

Conclusions: The optimal treatment for spinal cord astrocytoma is maximal tumor resection without neurological impairment. When some tumor remains in patients with an MIB-1 SI less than 4.0%, a wait-and-see approach is optimal. If the MIB-1 SI is higher than 4.0%, local radiation therapy is recommended. Adjuvant chemotherapy is not recommended for the treatment of grade II spinal cord astrocytoma.

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来源期刊
Journal of neurosurgery. Spine
Journal of neurosurgery. Spine 医学-临床神经学
CiteScore
5.10
自引率
10.70%
发文量
396
审稿时长
6 months
期刊介绍: Primarily publish original works in neurosurgery but also include studies in clinical neurophysiology, organic neurology, ophthalmology, radiology, pathology, and molecular biology.
期刊最新文献
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