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首页> 外文期刊>Pathology oncology research: POR >Boost Irradiation Integrated to Whole Brain Radiotherapy in the Management of Brain Metastases
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Boost Irradiation Integrated to Whole Brain Radiotherapy in the Management of Brain Metastases

机译:促进脑部转移管理中的全脑放射疗法的辐照

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Our retrospective analysis aimed to evaluate the clinical value of dose intensification schemes: WBRT and consecutive, delayed, or simultaneous integrated boost (SIB) in brain metastasis (BM) management. Clinical data and overall survival (OS) of 468 patients with BM from various primaries treated with 10 x 3 Gy WBRT (n = 195), WBRT+ 10 x 2 Gy boost (n = 125), or simultaneously 15 x 2.2 Gy WBRT+0.7 Gy boost (n = 148) during a 6-year period were statistically analysed. Significant difference in OS could be detected with additional boost to WBRT (3.3 versus 6.5 months) and this difference was confirmed for BMs of lung cancer and melanoma and both for oligo- and multiplex lesions. The OS was prolonged for the RPA 2 and RPA3 categories, if patients received escalated dose, 4.0 vs. 7.7 months; (p = 0.002) in class RPA2 and 2.6 vs. 4.2 months; (p < 0.0001) in the class RPA 3 respectively. The significant difference in OS was also achieved with SIB. The shortened overall treatment time of SIB with lower WBRT fraction dose exhibited survival benefit over WBRT alone, and could be applied for patients developing BM even with unfavourable prognostic factors. These results warrant for further study of this approach with dose escalation using the lately available solutions for hippocampus sparing and fractionated stereotactic irradiation. The simultaneous delivery of WBRT with reduced fraction dose and boost proved to be advantageous prolonging the OS with shortened treatment time and reduced probability for cognitive decline development even for patients with poor performance status and progressing extracranial disease.
机译:我们的回顾性分析旨在评估剂量强化方案的临床价值:WBRT和脑转移(BM)管理中的连续,延迟或同时的集成升压(SIB)。 468名患者的临床资料和整体存活(OS)来自各种原初级的BM患者(n = 195),WBRT + 10 x 2 Gy升压(n = 125),或同时15 x 2.2 gy wbrt + 0.7在6年期间,GY Boost(n = 148)在统计学上分析。可以通过额外提升到WBRT(3.3与6.5个月)来检测OS的显着差异,并且对肺癌和黑色素瘤的BMS确认了这种差异,并且用于寡糖和多重病变。如果患者接受升级的剂量,4.0与7.7个月,则延长OS为RPA 2和RPA3类别。 (p = 0.002)在RPA2类和2.6 VS. 4.2个月内; (P <0.0001)分别在RPA 3中。 SIB也实现了OS的显着差异。 Sib的缩短总处理时间较低的WBRT级分剂量在单独的WBRT上表现出存活,并且即使具有不利的预后因素,也可以应用于开发BM的患者。这些结果有助于进一步研究这种方法,使用最近可用的海马备件和分馏立体定向辐射的可用解决方案进行了剂量升级。随着额外的馏分剂量和增强剂的同时递送WBRT,并提升是有利的延长治疗时间,即使对于性能状况差和颅外疾病的患者,也甚至是认知性下降发展的概率。

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