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全身放疗联合全身boost 照射治疗脑转移瘤。

Boost Irradiation Integrated to Whole Brain Radiotherapy in the Management of Brain Metastases.

机构信息

Department of Oncotherapy, University of Szeged, Korányi fasor 12, Szeged, H-6720, Hungary.

Department of Pathology, University of Szeged, Állomás utca 1, Szeged, H-6725, Hungary.

出版信息

Pathol Oncol Res. 2020 Jan;26(1):149-157. doi: 10.1007/s12253-018-0383-y. Epub 2018 Jan 17.

Abstract

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 × 3 Gy WBRT (n = 195), WBRT+ 10 × 2 Gy boost (n = 125), or simultaneously 15 × 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.

摘要

我们的回顾性分析旨在评估剂量强化方案的临床价值

全脑放疗(WBRT)联合连续、延迟或同时的整合增敏(SIB)在脑转移瘤(BM)治疗中的作用。对 6 年内来自不同原发灶的 468 例 BM 患者的临床数据和总生存(OS)进行了回顾性分析,这些患者分别接受了 10×3 Gy 的 WBRT(n=195)、WBRT+10×2 Gy 推量(n=125)或同时接受 15×2.2 Gy WBRT+0.7 Gy 推量(n=148)。结果显示,与单纯 WBRT 相比,额外的 WBRT 推量可显著提高 OS(3.3 个月 vs. 6.5 个月),这一差异在肺癌和黑色素瘤的 BM 中得到了证实,同时在寡转移和多灶转移中也是如此。如果患者接受了递增剂量,那么 RPA 2 和 RPA 3 类别的 OS 会延长,4.0 个月 vs. 7.7 个月(p=0.002),RPA 2 类中为 2.6 个月 vs. 4.2 个月(p<0.0001);SIB 也能显著提高 OS。SIB 可显著缩短治疗时间,同时降低 WBRT 分割剂量,与单纯 WBRT 相比,可使生存获益,甚至可用于伴有不利预后因素的 BM 患者。这些结果表明,对于 SIB 联合剂量递增方案,需要进一步研究,包括最近可用于海马保护和分次立体定向放疗的解决方案。与单纯 WBRT 相比,降低 WBRT 分割剂量并联合推量治疗可显著延长 OS,同时缩短治疗时间,降低认知功能下降的发生概率,即使对于一般状况较差且合并颅外疾病进展的患者也是如此。

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