首页> 美国卫生研究院文献>Springer Open Choice >Radiotherapy and temozolomide for newly diagnosed glioblastoma and anaplastic astrocytoma: validation of Radiation Therapy Oncology Group-Recursive Partitioning Analysis in the IMRT and temozolomide era
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Radiotherapy and temozolomide for newly diagnosed glioblastoma and anaplastic astrocytoma: validation of Radiation Therapy Oncology Group-Recursive Partitioning Analysis in the IMRT and temozolomide era

机译:放疗和替莫唑胺用于新诊断的胶质母细胞瘤和间变性星形细胞瘤:在IMRT和替莫唑胺时代的放射治疗肿瘤学组-递归划分分析的验证

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摘要

Since the development of the Radiation Therapy Oncology Group-Recursive Partitioning Analysis (RTOG-RPA) risk classes for high-grade glioma, radiation therapy in combination with temozolomide (TMZ) has become standard care. While this combination has improved survival, the prognosis remains poor in the majority of patients. Therefore, strong interest in high-grade gliomas from basic research to clinical trials persists. We sought to evaluate whether the current RTOG-RPA retains prognostic significance in the TMZ era or alternatively, if modifications better prognosticate the optimal selection of patients with similar baseline prognosis for future clinical protocols. The records of 159 patients with newly-diagnosed glioblastoma (GBM, WHO grade IV) or anaplastic astrocytoma (AA, WHO grade III) were reviewed. Patients were treated with intensity-modulated radiation therapy (IMRT) and concurrent followed by adjuvant TMZ (n = 154) or adjuvant TMZ only (n = 5). The primary endpoint was overall survival. Three separate analyses were performed: (1) application of RTOG-RPA to the study cohort and calculation of subsequent survival curves, (2) fit a new tree model with the same predictors in RTOG-RPA, and (3) fit a new tree model with an expanded predictor set. All analyses used a regression tree analysis with a survival outcome fit to formulate new risk classes. Overall median survival was 14.9 months. Using the RTOG-RPA, the six classes retained their relative prognostic significance and overall ordering, with the corresponding survival distributions significantly different from each other (P < 0.01, χ2 statistic = 70). New recursive partitioning limited to the predictors in RTOG-RPA defined four risk groups based on Karnofsky Performance Status (KPS), histology, age, length of neurologic symptoms, and mental status. Analysis across the expanded predictors defined six risk classes, including the same five variables plus tumor location, tobacco use, and hospitalization during radiation therapy. Patients with excellent functional status, AA, and frontal lobe tumors had the best prognosis. For patients with newly-diagnosed high-grade gliomas, RTOG-RPA classes retained prognostic significance in patients treated with TMZ and IMRT. In contrast to RTOG-RPA, in our modified RPA model, KPS rather than age represented the initial split. New recursive partitioning identified potential modifications to RTOG-RPA that should be further explored with a larger data set.
机译:自从放射治疗肿瘤学组递归分区分析(RTOG-RPA)针对高级别神经胶质瘤的风险类别开发以来,放射疗法与替莫唑胺(TMZ)的结合已成为标准治疗方法。虽然这种组合可以提高生存率,但大多数患者的预后仍然很差。因此,对从基础研究到临床试验的高级神经胶质瘤的浓厚兴趣一直存在。我们试图评估当前的RTOG-RPA是否在TMZ时代保留了预后意义,或者是否可以通过修改更好地预测出具有相似基线预后的患者的最佳选择,以用于将来的临床方案。回顾了159例新诊断的胶质母细胞瘤(GBM,WHO IV级)或间变性星形细胞瘤(AA,WHO III级)患者的记录。患者接受了调强放射疗法(IMRT)的治疗,并同时接受佐剂TMZ(n = 154)或仅佐剂TMZ(n = 5)。主要终点是总体生存率。进行了三个单独的分析:(1)将RTOG-RPA应用于研究队列并计算随后的生存曲线;(2)在RTOG-RPA中采用具有相同预测因子的新树模型,以及(3)拟合新树具有扩展预测变量集的模型。所有分析均使用回归树分析和适合的生存结果来制定新的风险类别。总体中位生存期为14.9个月。使用RTOG-RPA,这6个类别保留了其相对的预后意义和整体排序,相应的生存分布彼此显着不同(P <0.01,χ 2 统计= 70)。新的递归划分仅限于RTOG-RPA中的预测因子,根据Karnofsky绩效状态(KPS),组织学,年龄,神经系统症状的持续时间和精神状态定义了四个风险组。对扩展的预测因素进行的分析定义了六种风险类别,包括相同的五个变量以及肿瘤位置,吸烟和放疗期间的住院治疗。具有良好功能状态,AA和额叶肿瘤的患者预后最佳。对于新诊断的高级别神经胶质瘤患者,在用TMZ和IMRT治疗的患者中,RTOG-RPA类保留了预后意义。与RTOG-RPA相比,在我们修改的RPA模型中,KPS而非年龄代表了初始划分。新的递归分区确定了对RTOG-RPA的潜在修改,应使用更大的数据集进一步探索。

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