Lo Simon S, Halasz Lia M, Choi Serah, Kumthekar Priya, Wang Tony J C, Shu Hui-Kuo, Sloan Andrew E, Olson Jeffrey J
Departments of Radiation Oncology and Neurological Surgery, University of Washington School of Medicine, 1959 NE Pacific Street, Box 356043, Seattle, WA, 98195, USA.
Department of Radiation Oncology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
J Neurooncol. 2025 Jul 24. doi: 10.1007/s11060-025-05074-1.
These recommendations apply to adults with newly diagnosed WHO Grade 2 diffuse glioma. Questions and Recommendations from the Prior Version of These Guidelines Without Change Question What is the optimal role of external beam radiotherapy in the management of adult patients with newly diagnosed low-grade glioma (LGG) in terms of improving outcome (i.e. survival, complications, seizure control or other reported outcomes of interest)?Recommendations Level I Radiotherapy is recommended in the management of newly diagnosed low-grade glioma in adults to prolong progression free survival, irrespective of extent of resection.Level II Radiotherapy is recommended in the management of newly diagnosed low grade glioma in adults as an equivalent alternative to observation in preserving cognitive function, irrespective of extent of resection.Level III Radiotherapy is recommended in the management of newly diagnosed low grade glioma in adults to improve seizure control in patients with epilepsy and subtotal resection.Level III Radiotherapy is recommended in the management of newly diagnosed low-grade glioma in adults to prolong overall survival in patients with subtotal resection.Level III Consideration of the risk of radiation induced morbidity, including cognitive decline, imaging abnormalities, metabolic dysfunction and malignant transformation, is recommended when the delivery of radiotherapy is selected in the management of newly diagnosed low grade glioma in adults.Question Which radiation strategies (dose, timing, fractionation, stereotactic radiation, brachytherapy, chemotherapy) improve outcomes compared to standard external beam radiation therapy in the initial management of low grade gliomas in adults?Recommendations Level I Lower dose radiotherapy is recommended as an equivalent alternative to higher dose immediate postoperative radiotherapy (45-50.4 vs. 59.4-64.8 Gy) in the management of newly diagnosed low-grade glioma in adults with reduced toxicity.Level III Delaying radiotherapy until recurrence or progression is recommended as an equivalent alternative to immediate postoperative radiotherapy in the management of newly diagnosed low-grade glioma in adults but may result in shorter time to progression.Level III The addition of chemotherapy to radiotherapy is not recommended over whole brain radiotherapy alone in the management of low-grade glioma, as it provides no additional survival benefit.Level III Limited-field radiotherapy is recommended over whole brain radiotherapy in the management of low-grade glioma.Level III Either stereotactic radiosurgery or brachytherapy are recommended as acceptable alternatives to external radiotherapy in selected patients.Question Do specific factors (e.g. age, volume, extent of resection, genetic subtype) identify subgroups with better outcomes following radiation therapy than the general population of adults with newly diagnosed low-grade gliomas?Recommendations Level II It is recommended that age greater than 40 years, astrocytic pathology, diameter greater than 6 cm, tumor crossing the midline and preoperative neurological deficit be considered as negative prognostic indicators when predicting overall survival in adult low grade glioma patients treated with radiotherapy.Level II It is recommended that smaller tumor size, extent of surgical resection and higher mini-mental status exam be considered as positive prognostic indicators when predicting overall survival and progression free survival in patients in adult low grade glioma patients treated with radiotherapy.Level II I It is recommended that seizures at presentation, presence of oligodendroglial histological component and 1p19q deletion (along with additional relevant factors-see Table 1) be considered as positive prognostic indicators when predicting response to radiotherapy in adults with low grade gliomas. Level III It is recommended that increasing age, decreasing performance status, decreasing cognition, presence of astrocytic histological component (along with additional relevant factors (see Tables 1, 2) be considered as negative prognostic indicators when predicting response to radiotherapy. New Questions and RecommendationsQuestion In adult patients with pathology confirmed WHO Grade 2 diffuse glioma is proton therapy superior to standard radiation therapy result in terms of overall survival, progression free survival, local control, complications, neurocognitive preservation, and quality of life (QOL)?Recommendation There is insufficient evidence to provide guidance on the superiority or inferiority of proton radiation effect compared to standard radiation therapy on WHO Grade 2 diffuse glioma in terms of overall survival, progression free survival, local control, complications, neurocognitive preservation, and quality of life.Question In adult patients with pathology confirmed WHO Grade 2 diffuse glioma receiving radiotherapy, do the molecular markers IDH-1 status, MGMT promoter methylation status and 1p19q presence or absence result in better prediction of overall survival, progression free survival, local control, complications, neurocognitive preservation, and quality of life?Recommendation Level III It is suggested that 1p/19q deletion status be used as a positive prognostic indicator regarding the effect of radiation therapy on progression free survival and overall survival for WHO grade II diffuse gliomas.
这些建议适用于新诊断为世界卫生组织2级弥漫性胶质瘤的成人患者。
这些指南先前版本中的问题及建议,无变化内容如下:
就改善预后(即生存、并发症、癫痫控制或其他报告的相关结果)而言,外照射放疗在新诊断的成人低级别胶质瘤(LGG)治疗中最理想的作用是什么?
推荐对新诊断的成人低级别胶质瘤进行放疗,以延长无进展生存期,无论切除范围如何。
推荐对新诊断的成人低级别胶质瘤进行放疗,作为在保留认知功能方面与观察等效的替代方案,无论切除范围如何。
推荐对新诊断的成人低级别胶质瘤进行放疗,以改善癫痫患者及次全切除患者的癫痫控制。
推荐对新诊断的成人低级别胶质瘤进行放疗,以延长次全切除患者的总生存期。
在选择对新诊断的成人低级别胶质瘤进行放疗时,建议考虑放射诱导的发病风险,包括认知功能下降、影像学异常、代谢功能障碍和恶性转化。
与标准外照射放疗相比,哪些放疗策略(剂量、时机、分割、立体定向放疗、近距离放疗、化疗)在成人低级别胶质瘤的初始治疗中能改善预后?
推荐低剂量放疗作为毒性较低的等效替代方案,用于治疗新诊断的成人低级别胶质瘤,替代高剂量术后即刻放疗(45 - 50.4 Gy对比59.4 - 64.8 Gy)。
建议将放疗推迟至复发或进展时进行,作为新诊断的成人低级别胶质瘤术后即刻放疗的等效替代方案,但可能会导致进展时间缩短。
在低级别胶质瘤治疗中,不推荐在放疗基础上加用化疗,因为其不会带来额外的生存获益。
在低级别胶质瘤治疗中,推荐局部野放疗而非全脑放疗。
对于特定患者,推荐立体定向放射外科或近距离放疗作为外照射放疗的可接受替代方案。
特定因素(如年龄、体积、切除范围、基因亚型)是否能识别出接受放疗后预后优于新诊断的成人低级别胶质瘤总体人群的亚组?
在预测接受放疗的成人低级别胶质瘤患者的总生存期时,建议将年龄大于40岁、星形细胞病理类型、直径大于6 cm、肿瘤跨越中线和术前神经功能缺损视为不良预后指标。
在预测接受放疗的成人低级别胶质瘤患者的总生存期和无进展生存期时,建议将较小的肿瘤大小、手术切除范围和较高的简易精神状态检查结果视为良好预后指标。
在预测成人低级别胶质瘤患者对放疗的反应时,建议将出现癫痫、少突胶质细胞组织学成分的存在以及1p19q缺失(以及其他相关因素 - 见表表)视为良好预后指标。
在预测对放疗的反应时,建议将年龄增加、身体状况下降、认知能力下降、星形细胞组织学成分的存在(以及其他相关因素(见表1、表2)视为不良预后指标。
新问题及建议
在病理确诊为世界卫生组织2级弥漫性胶质瘤的成人患者中,质子治疗在总生存期、无进展生存期、局部控制、并发症、神经认知功能保留和生活质量(QOL)方面是否优于标准放疗?
在总生存期、无进展生存期、局部控制、并发症、神经认知功能保留和生活质量方面,与标准放疗相比,质子放疗对世界卫生组织2级弥漫性胶质瘤疗效的优劣尚无足够证据提供指导。
在接受放疗的病理确诊为世界卫生组织2级弥漫性胶质瘤的成人患者中,分子标志物异柠檬酸脱氢酶-1(IDH-1)状态、O-6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子甲基化状态以及1p19q的有无能否更好地预测总生存期、无进展生存期、局部控制、并发症、神经认知功能保留和生活质量?
建议将1p/19q缺失状态作为世界卫生组织2级弥漫性胶质瘤放疗对无进展生存期和总生存期影响的良好预后指标。