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IDH 野生型胶质母细胞瘤的立体定向放射外科治疗:一项国际多中心研究。

Stereotactic radiosurgery for IDH wild type glioblastoma: an international, multicenter study.

机构信息

Department of Neurosurgery, University of Virginia, Charlottesville, VA, USA.

Department of Neurosurgery, NYU Langone Health, New York, USA.

出版信息

J Neurooncol. 2021 Dec;155(3):343-351. doi: 10.1007/s11060-021-03883-8. Epub 2021 Nov 19.

Abstract

OBJECTIVE

Isocitrate dehydrogenase (IDH) mutation status is recommended used for diagnosis and prognostication of glioblastoma patients. We studied efficacy and safety of stereotactic radiosurgery (SRS) for patients with recurrent IDH-wt glioblastoma.

METHODS

Consecutive patients treated with SRS for IDH-wt glioblastoma were pooled for this retrospective observational international multi-institutional study from institutions participating in the International Radiosurgery Research Foundation.

RESULTS

Sixty patients (median age 61 years) underwent SRS (median dose 15 Gy and median treatment volume: 7.01 cm) for IDH-wt glioblastoma. All patients had histories of surgery and chemotherapy with temozolomide, and 98% underwent fractionated radiation therapy. MGMT status was available for 42 patients, of which half of patients had MGMT mutant glioblastomas. During median post-SRS imaging follow-up of 6 months, 52% of patients experienced tumor progression. Median post-SRS progression free survival was 4 months. SRS prescription dose of > 14 Gy predicted longer progression free survival [HR 0.357 95% (0.164-0.777) p = 0.009]. Fifty-percent of patients died during post-SRS clinical follow-up that ranged from 1 to 33 months. SRS treatment volume of > 5 cc emerged as an independent predictor of shorter post-SRS overall survival [HR 2.802 95% CI (1.219-6.444) p = 0.02]. Adverse radiation events (ARE) suggestive of radiation necrosis were diagnosed in 6/55 (10%) patients and were managed conservatively in the majority of patients.

CONCLUSIONS

SRS prescription dose of > 14 Gy is associated with longer progression free survival while tumor volume of > 5 cc is associated with shorter overall survival after SRS for IDH-wt glioblastomas. AREs are rare and are typically managed conservatively.

摘要

目的

异柠檬酸脱氢酶(IDH)突变状态被推荐用于胶质母细胞瘤患者的诊断和预后判断。本研究旨在探讨替莫唑胺化疗后复发的 IDH 野生型胶质母细胞瘤患者接受立体定向放射外科(SRS)治疗的疗效和安全性。

方法

本回顾性观察性国际多中心研究纳入了来自国际放射外科研究基金会(IRSF)参与机构的连续接受 SRS 治疗的 IDH 野生型胶质母细胞瘤患者。

结果

60 例患者(中位年龄 61 岁)接受了 SRS 治疗(中位剂量 15Gy,中位治疗体积 7.01cm³)。所有患者均有手术和替莫唑胺化疗史,98%的患者接受了分割放疗。42 例患者的 MGMT 状态可评估,其中一半患者的胶质母细胞瘤为 MGMT 突变型。在中位 SRS 后 6 个月的影像学随访期间,52%的患者发生肿瘤进展。中位 SRS 后无进展生存期为 4 个月。SRS 处方剂量>14Gy 可预测更长的无进展生存期[风险比(HR)0.357,95%可信区间(CI)0.164-0.777,p=0.009]。在 SRS 后临床随访的 1-33 个月期间,50%的患者死亡。SRS 治疗体积>5cc 是 SRS 后总生存期较短的独立预测因素[HR 2.802,95%CI(1.219-6.444),p=0.02]。6/55(10%)例患者诊断出提示放射性坏死的放射性不良反应(ARE),多数患者采用保守治疗。

结论

SRS 处方剂量>14Gy 与无进展生存期延长相关,而 SRS 治疗后肿瘤体积>5cc 与总生存期缩短相关。ARE 罕见,通常采用保守治疗。

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