Department of Neurosurgery, Thomas Jefferson University, Philadelphia, PA, USA.
Department of Radiation Oncology, Thomas Jefferson University, Philadelphia, PA, USA.
J Neurooncol. 2020 Nov;150(2):269-359. doi: 10.1007/s11060-020-03607-4. Epub 2020 Nov 19.
These recommendations apply to adult patients with newly diagnosed or suspected glioblastoma.
Question What imaging modalities are in development that may be able to provide improvements in diagnosis, and therapeutic guidance for individuals with newly diagnosed glioblastoma?
Level III: It is suggested that techniques utilizing magnetic resonance imaging for diffusion weighted imaging, and to measure cerebral blood and magnetic spectroscopic resonance imaging of N-acetyl aspartate, choline and the choline to N-acetyl aspartate index to assist in diagnosis and treatment planning in patients with newly diagnosed or suspected glioblastoma.
Question What new surgical techniques can be used to provide improved tumor definition and resectability to yield better tumor control and prognosis for individuals with newly diagnosed glioblastoma?
Level II: The use of 5-aminolevulinic acid is recommended to improve extent of tumor resection in patients with newly diagnosed glioblastoma. Level II: The use of 5-aminolevulinic acid is recommended to improve median survival and 2 year survival in newly diagnosed glioblastoma patients with clinical characteristics suggesting poor prognosis. Level III: It is suggested that, when available, patients be enrolled in properly designed clinical trials assessing the value of diffusion tensor imaging in improving the safety of patients with newly diagnosed glioblastoma undergoing surgery.
Question What new pathology techniques and measurement of biomarkers in tumor tissue can be used to provide improved diagnostic ability, and determination of therapeutic responsiveness and prognosis for patients with newly diagnosed glioblastomas?
Level II: Assessment of tumor MGMT promoter methylation status is recommended as a significant predictor of a longer progression free survival and overall survival in patients with newly diagnosed with glioblastoma. Level II: Measurement of tumor expression of neuron-glia-2, neurofilament protein, glutamine synthetase and phosphorylated STAT3 is recommended as a predictor of overall survival in patients with newly diagnosed with glioblastoma. Level III: Assessment of tumor IDH1 mutation status is suggested as a predictor of longer progression free survival and overall survival in patients with newly diagnosed with glioblastoma. Level III: Evaluation of tumor expression of Phosphorylated Mitogen-Activated Protein Kinase protein, EGFR protein, and Insulin-like Growth Factor-Binding Protein-3 is suggested as a predictor of overall survival in patients with newly diagnosed with glioblastoma.
Question What radiation therapy techniques are in development that may be used to provide improved tumor control and prognosis for individuals with newly diagnosed glioblastomas?
Level III: It is suggested that patients with newly diagnosed glioblastoma undergo pretreatment radio-labeled amino acid tracer positron emission tomography to assess areas at risk for tumor recurrence to assist in radiation treatment planning. Level III: It is suggested that, when available, patients be with newly diagnosed glioblastomas be enrolled in properly designed clinical trials of radiation dose escalation, altered fractionation, or new radiation delivery techniques.
Question What emerging chemotherapeutic agents or techniques are available to provide better tumor control and prognosis for patients with newly diagnosed glioblastomas?
Level III: As no emerging chemotherapeutic agents or techniques were identified in this review that improved tumor control and prognosis it is suggested that, when available, patients with newly diagnosed glioblastomas be enrolled in properly designed clinical trials of chemotherapy.
Question What new targeted therapy agents are available to provide better tumor control and prognosis for individuals with newly diagnosed glioblastomas?
Level III: As no new molecular and targeted therapies have clearly provided better tumor control and prognosis it is suggested that, when available, patients with newly diagnosed glioblastomas be enrolled in properly designed clinical trials of molecular and targeted therapies IMMUNOTHERAPY: Question What emerging immunotherapeutic agents or techniques are available to provide better tumor control and prognosis for patients with newly diagnosed glioblastomas?
Level III: As no immunotherapeutic agents have clearly provided better tumor control and prognosis it is suggested that, when available, patients with newly diagnosed glioblastomas be enrolled in properly designed clinical trials of immunologically-based therapies.
Question What novel therapies or techniques are in development to provide better tumor control and prognosis for individuals with newly diagnosed glioblastomas?
Level II: The use of tumor-treating fields is recommended for patients with newly diagnosed glioblastoma who have undergone surgical debulking and completed concurrent chemoradiation without progression of disease at the time of tumor-treating field therapy initiation. Level II: It is suggested that, when available, enrollment in properly designed studies of vector containing herpes simplex thymidine kinase gene and prodrug therapies be considered in patients with newly diagnosed glioblastoma.
这些建议适用于新诊断或疑似胶质母细胞瘤的成年患者。
问题有哪些正在开发中的成像方式可能能够提高新诊断的胶质母细胞瘤的诊断准确性,并为治疗提供指导?
III 级:建议利用磁共振成像中的弥散加权成像技术,以及测量脑血流和磁共振波谱成像中的 N-乙酰天门冬氨酸、胆碱和胆碱与 N-乙酰天门冬氨酸指数,以协助新诊断或疑似胶质母细胞瘤患者的诊断和治疗计划。
问题有哪些新的手术技术可以用于提高肿瘤的定义和可切除性,从而更好地控制肿瘤并改善新诊断的胶质母细胞瘤患者的预后?
II 级:建议在新诊断的胶质母细胞瘤患者中使用 5-氨基乙酰丙酸来提高肿瘤切除范围。II 级:建议在有临床预后不良特征的新诊断的胶质母细胞瘤患者中使用 5-氨基乙酰丙酸,以延长中位生存期和 2 年生存率。III 级:建议在适当设计的临床试验中评估扩散张量成像在提高新诊断的胶质母细胞瘤患者手术安全性方面的价值,当有条件时,建议患者参与这些临床试验。
问题有哪些新的病理技术和肿瘤组织中的生物标志物测量方法可以用于提高诊断能力,并确定新诊断的胶质母细胞瘤患者的治疗反应和预后?
II 级:评估肿瘤 MGMT 启动子甲基化状态作为预测新诊断的胶质母细胞瘤患者无进展生存期和总生存期的重要指标。II 级:测量肿瘤中神经元-神经胶质-2、神经丝蛋白、谷氨酰胺合成酶和磷酸化 STAT3 的表达,作为预测新诊断的胶质母细胞瘤患者总生存期的指标。III 级:评估肿瘤 IDH1 突变状态作为预测新诊断的胶质母细胞瘤患者无进展生存期和总生存期的指标。III 级:评估肿瘤中磷酸化丝裂原活化蛋白激酶蛋白、EGFR 蛋白和胰岛素样生长因子结合蛋白-3 的表达,作为预测新诊断的胶质母细胞瘤患者总生存期的指标。
问题有哪些正在开发中的放射治疗技术可能用于提高新诊断的胶质母细胞瘤患者的肿瘤控制和预后?
III 级:建议新诊断的胶质母细胞瘤患者在进行预处理放射性氨基酸示踪剂正电子发射断层扫描,以评估肿瘤复发的风险区域,协助放射治疗计划。III 级:建议在适当设计的临床试验中,对新诊断的胶质母细胞瘤患者进行放射剂量递增、改变分割方式或新的放射治疗技术的评估。
问题有哪些新的化疗药物或技术可用于提高新诊断的胶质母细胞瘤患者的肿瘤控制和预后?
III 级:由于本综述中未发现任何改善肿瘤控制和预后的新化疗药物或技术,因此建议在适当设计的临床试验中,对新诊断的胶质母细胞瘤患者进行化疗。
问题有哪些新的靶向治疗药物可用于提高新诊断的胶质母细胞瘤患者的肿瘤控制和预后?
III 级:由于没有新的分子靶向治疗方法明确提高了肿瘤控制和预后,因此建议在适当设计的临床试验中,对新诊断的胶质母细胞瘤患者进行分子靶向治疗。
问题有哪些新的免疫治疗药物或技术可用于提高新诊断的胶质母细胞瘤患者的肿瘤控制和预后?
III 级:由于没有免疫治疗药物明确提高了肿瘤控制和预后,因此建议在适当设计的临床试验中,对新诊断的胶质母细胞瘤患者进行免疫治疗。
问题有哪些新的治疗方法或技术正在开发中,以提高新诊断的胶质母细胞瘤患者的肿瘤控制和预后?
II 级:在新诊断的胶质母细胞瘤患者中,在肿瘤治疗场治疗开始时,如果患者没有疾病进展,且已完成手术切除和同期放化疗,则推荐使用肿瘤治疗场。II 级:建议在适当设计的研究中,在新诊断的胶质母细胞瘤患者中使用含有单纯疱疹胸腺嘧啶激酶基因和前药治疗的载体。