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成人弥漫性星形细胞瘤和少突胶质细胞瘤的治疗:美国临床肿瘤学会-神经肿瘤学会指南

Therapy for Diffuse Astrocytic and Oligodendroglial Tumors in Adults: ASCO-SNO Guideline.

作者信息

Mohile Nimish A, Messersmith Hans, Gatson Na Tosha, Hottinger Andreas F, Lassman Andrew, Morton Jordan, Ney Douglas, Nghiemphu Phioanh Leia, Olar Adriana, Olson Jeffery, Perry James, Portnow Jana, Schiff David, Shannon Anne, Shih Helen A, Strowd Roy, van den Bent Martin, Ziu Mateo, Blakeley Jaishri

机构信息

Department of Neurology and Wilmot Cancer Institute, University of Rochester Medical Center, Rochester, NY.

American Society of Clinical Oncology, Alexandria, VA.

出版信息

J Clin Oncol. 2022 Feb 1;40(4):403-426. doi: 10.1200/JCO.21.02036. Epub 2021 Dec 13.

Abstract

PURPOSE

To provide guidance to clinicians regarding therapy for diffuse astrocytic and oligodendroglial tumors in adults.

METHODS

ASCO and the Society for Neuro-Oncology convened an Expert Panel and conducted a systematic review of the literature.

RESULTS

Fifty-nine randomized trials focusing on therapeutic management were identified.

RECOMMENDATIONS

Adults with newly diagnosed oligodendroglioma, isocitrate dehydrogenase (IDH)-mutant, 1p19q codeleted CNS WHO grade 2 and 3 should be offered radiation therapy (RT) and procarbazine, lomustine, and vincristine (PCV). Temozolomide (TMZ) is a reasonable alternative for patients who may not tolerate PCV, but no high-level evidence supports upfront TMZ in this setting. People with newly diagnosed astrocytoma, IDH-mutant, 1p19q non-codeleted CNS WHO grade 2 should be offered RT with adjuvant chemotherapy (TMZ or PCV). People with astrocytoma, IDH-mutant, 1p19q non-codeleted CNS WHO grade 3 should be offered RT and adjuvant TMZ. People with astrocytoma, IDH-mutant, CNS WHO grade 4 may follow recommendations for either astrocytoma, IDH-mutant, 1p19q non-codeleted CNS WHO grade 3 or glioblastoma, IDH-wildtype, CNS WHO grade 4. Concurrent TMZ and RT should be offered to patients with newly diagnosed glioblastoma, IDH-wildtype, CNS WHO grade 4 followed by 6 months of adjuvant TMZ. Alternating electric field therapy, approved by the US Food and Drug Administration, should be considered for these patients. Bevacizumab is not recommended. In situations in which the benefits of 6-week RT plus TMZ may not outweigh the harms, hypofractionated RT plus TMZ is reasonable. In patients age ≥ 60 to ≥ 70 years, with poor performance status or for whom toxicity or prognosis are concerns, best supportive care alone, RT alone (for promoter unmethylated tumors), or TMZ alone (for promoter methylated tumors) are reasonable treatment options. Additional information is available at www.asco.org/neurooncology-guidelines.

摘要

目的

为临床医生提供关于成人弥漫性星形细胞瘤和少突胶质细胞瘤治疗的指导。

方法

美国临床肿瘤学会(ASCO)和神经肿瘤学会召集了一个专家小组,并对文献进行了系统回顾。

结果

确定了59项关注治疗管理的随机试验。

建议

对于新诊断的异柠檬酸脱氢酶(IDH)突变、1p19q共缺失的中枢神经系统(CNS)WHO 2级和3级少突胶质细胞瘤成人患者,应给予放射治疗(RT)和丙卡巴肼、洛莫司汀和长春新碱(PCV)。替莫唑胺(TMZ)是不耐受PCV患者的合理替代方案,但在这种情况下,尚无高级别证据支持一线使用TMZ。新诊断的IDH突变、1p19q未共缺失的CNS WHO 2级星形细胞瘤患者,应给予RT联合辅助化疗(TMZ或PCV)。IDH突变、1p19q未共缺失的CNS WHO 3级星形细胞瘤患者,应给予RT和辅助TMZ。IDH突变的CNS WHO 4级星形细胞瘤患者可遵循IDH突变、1p19q未共缺失的CNS WHO 3级星形细胞瘤或IDH野生型的CNS WHO 4级胶质母细胞瘤的推荐。新诊断的IDH野生型的CNS WHO 4级胶质母细胞瘤患者应给予同步TMZ和RT,随后进行6个月的辅助TMZ治疗。对于这些患者,应考虑美国食品药品监督管理局批准的交变电场治疗。不推荐使用贝伐单抗。在6周RT加TMZ的益处可能不超过危害的情况下,短程分割RT加TMZ是合理的。对于年龄≥60至≥70岁、体能状态差或担心毒性或预后的患者,单纯最佳支持治疗、单纯RT(用于启动子未甲基化肿瘤)或单纯TMZ(用于启动子甲基化肿瘤)是合理的治疗选择。更多信息可在www.asco.org/neurooncology-guidelines查询。

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