在接受立体定向放射手术治疗脑转移的患者中,前期免疫治疗可降低脑转移速度。

IF 0.7 Q4 SURGERY
Journal of radiosurgery and SBRT Pub Date : 2022-01-01
Mohammed Abdulhaleem, Emmanuel Scott, Hannah Johnston, Scott Isom, Claire Lanier, Michael LeCompte, Christina K Cramer, Jimmy Ruiz, Hui-Wen Lo, Kuonosuke Watabe, Stacey O'Neill, Christopher Whitlow, Stephen B Tatter, Adrian W Laxton, Jing Su, Michael D Chan
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引用次数: 0

摘要

背景:虽然免疫治疗已被证明可以提高脑转移患者的生存率并减少神经系统死亡,但尚不清楚这种改善是否由于预防新的脑转移。方法:我们对首次诊断为转移性疾病的同时出现脑转移的患者进行了回顾性回顾,并将前期免疫治疗作为其治疗方案的一部分,并对脑转移进行了立体定向放射手术(SRS)。我们将该队列与历史对照人群(免疫治疗时代之前)进行了比较,这些人群接受了免疫治疗前的标准护理系统治疗和脑转移的SRS治疗。结果:与历史队列相比,接受前期免疫治疗的患者的中位总生存时间有所改善(48个月vs 8.4个月,p=0.001)。前期免疫治疗组和历史对照组发生远端脑衰竭的中位时间在统计学上是相等的(p=0.3)(10.3个月vs 12.6个月)。前期免疫治疗组的脑转移速度(平均每年3.72例转移)低于历史对照组(平均每年9.48例转移,p=0.001)。一年内神经系统死亡的累积发生率在前期免疫治疗组为12%,在历史对照组为28% (p=0.1)。结论:与历史对照组相比,前期免疫治疗似乎提高了总生存率,降低了BMV。虽然这些数据仍有待验证,但它们表明脑转移患者可能受益于SRS联合免疫治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Upfront immunotherapy leads to lower brain metastasis velocity in patients undergoing stereotactic radiosurgery for brain metastases.

Upfront immunotherapy leads to lower brain metastasis velocity in patients undergoing stereotactic radiosurgery for brain metastases.

Upfront immunotherapy leads to lower brain metastasis velocity in patients undergoing stereotactic radiosurgery for brain metastases.

Background: While immunotherapy has been shown to improve survival and decrease neurologic death in patients with brain metastases, it remains unclear whether this improvement is due to prevention of new metastasis to the brain.

Method: We performed a retrospective review of patients presenting with brain metastases simultaneously with the first diagnosis of metastatic disease and were treated with upfront immunotherapy as part of their treatment regimen and stereotactic radiosurgery (SRS) to the brain metastases. We compared this cohort with a historical control population (prior to the immunotherapy era) who were treated with pre-immunotherapy standard of care systemic therapy and with SRS to the brain metastases.

Results: Median overall survival time was improved in the patients receiving upfront immunotherapy compared to the historical cohort (48 months vs 8.4 months, p=0.001). Median time to distant brain failure was statistically equivalent (p=0.3) between the upfront immunotherapy cohort and historical control cohort (10.3 vs 12.6 months). Brain metastasis velocity was lower in the upfront immunotherapy cohort (median 3.72 metastases per year) than in the historical controls (median 9.48 metastases per year, p=0.001). Cumulative incidence of neurologic death at one year was 12% in the upfront immunotherapy cohort and 28% in the historical control cohort (p=0.1).

Conclusions: Upfront immunotherapy appears to improve overall survival and decrease BMV compared to historical controls. While these data remain to be validated, they suggest that brain metastasis patients may benefit from concurrent immunotherapy with SRS.

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CiteScore
1.40
自引率
8.30%
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