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Tumor histology and location predict deep nuclei toxicity: Implications for late effects from focal brain irradiation

机译:肿瘤的组织学和位置预测深核毒性:局灶性脑照射对晚期效应的影响

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Normal tissue toxicity resulting from both disease and treatment is an adverse side effect in the management of patients with central nervous system malignancies. We tested the hypothesis that despite these improvements, certain tumors place patients at risk for neurocognitive, neuroendocrine, and neurosensory late effects. Defining patient groups at risk for these effects could allow for development of preventive strategies. Fifty patients with primary brain tumors underwent radiation planning with magnetic resonance imaging scan and computed tomography datasets. Organs at risk (OAR) responsible for neurocognitive, neuroendocrine, and neurosensory function were defined. Inverse-planned intensity-modulated radiation therapy was optimized with priority given to target coverage while penalties were assigned to exceeding normal tissue tolerances. Tumor laterality, location, and histology were compared with OAR doses, and analysis of variance was performed to determine the significance of any observed correlation. The ipsilateral hippocampus exceeded dose limits in frontal (74%), temporal (94%), and parietal (100%) lobe tumor locations. The contralateral hippocampus was at risk in the following tumor locations: frontal (53%), temporal (83%), or parietal (50%) lobe. Patients with high-grade glioma were at risk for ipsilateral (88%) and contralateral (73%) hippocampal damage (P <0.05 compared with other histologies). The pituitary gland and hypothalamus exceeded dose tolerances in patients with pituitary tumors (both 100%) and high-grade gliomas (50% and 75%, P <0.05 compared with other histologies), respectively. Despite application of modern radiation therapy, certain tumor locations and histologies continue to place patients at risk for morbidity. Patients with high-grade gliomas or tumors located in the frontal, temporal, or parietal lobes are at risk for neurocognitive decline, likely because of larger target volumes and higher radiation doses. Data from this study may help to stratify patients at risk for late effects to develop strategies to reduce frequency and severity of radiation sequelae.
机译:由疾病和治疗引起的正常组织毒性是中枢神经系统恶性肿瘤患者管理中的不良副作用。我们测试了以下假设:尽管有这些改善,但某些肿瘤使患者处于神经认知,神经内分泌和神经感觉迟发效应的风险中。定义有这些效应风险的患者群体可以制定预防策略。 50名原发性脑肿瘤患者接受了磁共振成像扫描和计算机断层扫描数据集的辐射计划。定义了负责神经认知,神经内分泌和神经感觉功能的高危器官(OAR)。优化了逆计划的强度调制放射疗法,优先考虑了靶标的覆盖范围,同时对超出正常组织耐受性的惩罚进行了处罚。将肿瘤的侧面,位置和组织学与OAR剂量进行比较,并进行方差分析以确定任何观察到的相关性的显着性。同侧海马在额叶(74%),颞叶(94%)和顶叶(100%)肿瘤位置超出剂量限制。对侧海马在以下肿瘤部位处于危险中:额叶(53%),颞叶(83%)或顶叶(50%)。高度神经胶质瘤患者有同侧(88%)和对侧(73%)海马损伤的风险(与其他组织学相比,P <0.05)。垂体肿瘤(均为100%)和高度神经胶质瘤(分别为50%和75%,与其他组织学相比P <0.05)的患者的垂体和下丘脑均超出剂量耐受范围。尽管应用了现代放射疗法,某些肿瘤的位置和组织学继续使患者处于发病的风险中。位于额叶,颞叶或顶叶的高级别神经胶质瘤或肿瘤患者存在神经认知功能下降的风险,这可能是由于目标体积更大和放射剂量更高所致。这项研究的数据可能有助于对有后期影响风险的患者进行分层,以制定减少放射后遗症频率和严重程度的策略。

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