神经外科医师大会关于复发性弥漫性低级别胶质瘤治疗的系统回顾和循证指南:更新版。

IF 3.2 2区 医学 Q2 CLINICAL NEUROLOGY Journal of Neuro-Oncology Pub Date : 2024-10-14 DOI:10.1007/s11060-024-04838-5
Kevin Morrow, Andrew Sloan, Jeffrey J Olson, D Ryan Ormond
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引用次数: 0

摘要

这些建议适用于复发的WHO 2级浸润性弥漫性胶质瘤(少突胶质细胞瘤、星形细胞瘤)的成人患者。问题与建议:影像学问题1:对于组织学证实的WHO 2级弥漫性胶质瘤疑似复发的成人患者,与标准磁共振神经影像学相比,使用磁共振波谱、灌注加权成像、弥散加权成像或正电子发射计算机断层显像的高级影像学技术是否能提供更好的肿瘤复发和组织学进展评估?建议 III 级:对于组织学证实为 WHO 2 级弥漫性胶质瘤疑似复发的成人患者,建议使用磁共振波谱成像、灌注加权成像、弥散加权成像或 PET 等高级成像技术来鉴别肿瘤复发或组织学进展。病理问题 1:对于组织学证实的 WHO 2 级弥漫性胶质瘤疑似复发的成人患者,是否有必要进行 IDH-1、IDH-2 和 TP53 突变以及 MGMT 启动子甲基化突变的分子检测,以预测生存率并制定治疗建议?建议 III 级:建议为诊断目的确定 IDH 突变状态。TP53突变发生在WHO 2级弥漫性胶质瘤发病的早期,并保持稳定,不建议将其作为复发时恶性转化倾向的标志或其他预后指标。建议将 MGMT 状态评估作为评估预后的辅助手段。问题2:对于组织学证实为WHO 2级弥漫性胶质瘤的疑似复发成人患者,是否有必要检测增殖指数(MIB-1和/或BUdR)以预测生存率并制定治疗建议?建议 III 级:建议对 WHO 2 级弥漫性胶质瘤检测增殖指数(MIB-1 或 BUdR),因为增殖指数越高,复发的可能性越大,无进展生存期和总生存期越短。化疗问题1:对于组织学证实的WHO 2级弥漫性胶质瘤疑似复发的成人患者,在治疗方案中添加替莫唑胺(TMZ)、其他细胞毒性药物或靶向药物是否能改善PFS和/或OS?建议等级III:建议在治疗复发的WHO 2级弥漫性胶质瘤时使用替莫唑胺,因为它可以改善临床症状。建议将 PCV 用于治疗复发的 WHO 2 级弥漫性胶质瘤,因为它可以改善临床症状,其中证据最充分的是少突胶质瘤。建议将 TMZ 作为复发的 WHO 2 级弥漫性胶质瘤的初始选择。不建议使用卡铂,因为卡铂作为复发性WHO 2级弥漫性胶质瘤的单药治疗并无明显疗效。放疗问题1:对于组织学证实为WHO 2级弥漫性胶质瘤的疑似复发成人患者,在治疗方案中加入放疗是否能改善PFS和/或OS?建议等级III:如果既往未接受过放疗,建议在复发时进行放疗。问题2:对于既往接受过放疗、组织学证实为WHO 2级弥漫性胶质瘤疑似复发的成人患者,在治疗方案中增加再次放疗或质子治疗是否能改善PFS和/或OS?建议等级III:建议在WHO 2级弥漫性胶质瘤复发的情况下考虑再次放疗,因为它可能会为PFS和OS带来益处。 问题1:对于组织学证实为WHO 2级弥漫性胶质瘤疑似复发的成人患者,手术切除是否能改善PFS和/或OS?目前尚无足够证据就手术治疗的价值或切除范围与复发的WHO 2级弥漫性胶质瘤生存率的关系提出新的具体建议。
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Congress of Neurological Surgeons systematic review and evidence‑based guidelines on the management of recurrent diffuse low-grade glioma: update.

Target population These recommendations apply to adult patients with recurrent WHO grade 2 infiltrative diffuse glioma (oligodendroglioma, astrocytoma).Questions and Recommendations:Imaging Q1: In adult patients with suspected recurrence of histologically proven WHO grade 2 diffuse glioma, do advanced imaging techniques using magnetic resonance spectroscopy, perfusion weighted imaging, diffusion weighted imaging or PET provide superior assessment of tumor recurrence and histologic progression compared to standard MRI neuroimaging?Recommendation Level III: In adult patients with suspected recurrence of histologically proven WHO grade 2 diffuse glioma, advanced imaging techniques using magnetic resonance spectroscopy, perfusion weighted imaging, diffusion weighted imaging or PET are suggested for identification of tumor recurrence or histologic progression.Pathology Q1: In adult patients with suspected recurrence of histologically proven WHO grade 2 diffuse glioma, is molecular testing for IDH-1, IDH-2, and TP53 Mutations and MGMT promotor methylation mutation warranted for predicting survival and formulating treatment recommendations?Recommendation Level III: It is suggested that IDH mutation status be determined for diagnostic purposes. TP53 mutations occur early in WHO grade 2 diffuse glioma pathogenesis, remain stable, and are not suggested as a marker of predisposition to malignant transformation at recurrence or other measures of prognosis. Assessment of MGMT status is suggested as an adjunct to assessing prognosis. Assessment of CDK2NA status is suggested since this is associated with malignant progression of WHO grade 2 diffuse gliomas.Q2: In adult patients with suspected recurrence of histologically proven WHO Grade 2 diffuse glioma, is testing of proliferation indices (MIB-1 and/or BUdR) warranted for predicting survival and formulating treatment recommendations?Recommendation Level III: It is suggested that proliferative indices (MIB-1 or BUdR) be measured in WHO grade 2 diffuse glioma as higher proliferation indices are associated with increased likelihood of recurrence and shorter progression free and overall survival.Chemotherapy Q1: In adult patients with suspected recurrence of histologically proven WHO grade 2 diffuse glioma, does addition of temozolomide (TMZ), other cytotoxic agents or targeted agents to their treatment regimen improve PFS and/or OS?Recommendation Level III: Temozolomide is suggested in the therapy of recurrent WHO grade 2 diffuse glioma as it may improve clinical symptoms. PCV is suggested in the therapy of WHO grade 2 diffuse glioma at recurrence as it may improve clinical symptoms with the strongest evidence being for oligodendrogliomas. TMZ is suggested as the initial choice for recurrent WHO grade 2 diffuse glioma. Carboplatin is not suggested as there is no significant benefit from carboplatin as single agent therapy for recurrent WHO grade 2 diffuse gliomas. There is insufficient evidence to make any recommendations regarding other agents in the management of recurrent WHO grade 2 diffuse glioma.Radiotherapy Q1: In adult patients with suspected recurrence of histologically proven WHO grade 2 diffuse glioma, does addition of radiotherapy to treatment regimen improve PFS and/or OS?Recommendation Level III: Radiation is suggested at recurrence if there was no previous radiation treatment. Q2: In adult patients with suspected recurrence of histologically proven WHO grade 2 diffuse glioma after previous radiotherapy, does addition of re-irradiation or proton therapy to the treatment regimen improve PFS and/or OS?Recommendation Level III: It is suggested that re-irradiation be considered in the setting of WHO grade 2 diffuse glioma recurrence as it may provide benefit in PFS and OS.Surgery Q1: In adult patients with suspected recurrence of histologically proven WHO grade 2 diffuse glioma, does surgical resection improve PFS and/or OS?. There is insufficient evidence to make any new specific recommendations regarding the value of surgery or extent of resection in relationship to survival for recurrent WHO grade 2 diffuse glioma.

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来源期刊
Journal of Neuro-Oncology
Journal of Neuro-Oncology 医学-临床神经学
CiteScore
6.60
自引率
7.70%
发文量
277
审稿时长
3.3 months
期刊介绍: The Journal of Neuro-Oncology is a multi-disciplinary journal encompassing basic, applied, and clinical investigations in all research areas as they relate to cancer and the central nervous system. It provides a single forum for communication among neurologists, neurosurgeons, radiotherapists, medical oncologists, neuropathologists, neurodiagnosticians, and laboratory-based oncologists conducting relevant research. The Journal of Neuro-Oncology does not seek to isolate the field, but rather to focus the efforts of many disciplines in one publication through a format which pulls together these diverse interests. More than any other field of oncology, cancer of the central nervous system requires multi-disciplinary approaches. To alleviate having to scan dozens of journals of cell biology, pathology, laboratory and clinical endeavours, JNO is a periodical in which current, high-quality, relevant research in all aspects of neuro-oncology may be found.
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