Ali Mir Amaan, Hirshman Brian R, Wilson Bayard, Carroll Kate T, Proudfoot James A, Goetsch Steven J, Alksne John F, Ott Kenneth, Aiyama Hitoshi, Nagano Osamu, Carter Bob S, Fogarty Gerald, Hong Angela, Serizawa Toru, Yamamoto Masaaki, Chen Clark C
Center for Translational and Applied Neuro-Oncology, Department of Neurosurgery, University of California, San Diego, La Jolla, California, USA.
Clinical and Translational Research Institute, University of California, San Diego, San Diego, California, USA.
World Neurosurg. 2017 Nov;107:944-951.e1. doi: 10.1016/j.wneu.2017.07.062. Epub 2017 Jul 19.
The number of brain metastases (BMs) plays an important role in the decision between stereotactic radiosurgery (SRS) and whole-brain radiation therapy.
We analyzed the survival of 5750 SRS-treated patients with BM as a function of BM number. Survival analyses were performed with Kaplan-Meier analysis as well as univariate and multivariate Cox proportional hazards models.
Patients with BMs were first categorized as those with 1, 2-4, and 5-10 BMs based on the scheme proposed by Yamamoto et al. (Lancet Oncology 2014). Median overall survival for patients with 1 BM was superior to those with 2-4 BMs (7.1 months vs. 6.4 months, P = 0.009), and survival of patients with 2-4 BMs did not differ from those with 5-10 BMs (6.4 months vs. 6.3 months, P = 0.170). The median survival of patients with >10 BMs was lower than those with 2-10 BMs (6.3 months vs. 5.5 months, P = 0.025). In a multivariate model that accounted for age, Karnofsky Performance Score, systemic disease status, tumor histology, and cumulative intracranial tumor volume, we observed a ∼10% increase in hazard of death when comparing patients with 1 versus 2-10 BMs (P < 0.001) or 10 versus >10 BMs (P < 0.001). When BM number was modeled as a continuous variable rather than using the classification by Yamamoto et al., we observed a step-wise 4% increase in the hazard of death for every increment of 6-7 BM (P < 0.001).
The contribution of BM number to overall survival is modest and should be considered as one of the many variables considered in the decision between SRS and whole-brain radiation therapy.
脑转移瘤(BM)的数量在立体定向放射外科治疗(SRS)和全脑放射治疗的决策中起着重要作用。
我们分析了5750例接受SRS治疗的BM患者的生存情况,并将其作为BM数量的函数进行分析。生存分析采用Kaplan-Meier分析以及单变量和多变量Cox比例风险模型。
根据Yamamoto等人(《柳叶刀肿瘤学》2014年)提出的方案,将BM患者首先分为1个、2 - 4个和5 - 10个BM的患者。1个BM患者的中位总生存期优于2 - 4个BM的患者(7.1个月对6.4个月,P = 0.009),2 - 4个BM患者的生存期与5 - 10个BM的患者无差异(6.4个月对6.3个月,P = 0.170)。BM数量>10个的患者中位生存期低于2 - 10个BM的患者(6.3个月对5.5个月,P = 0.025)。在一个考虑了年龄、卡诺夫斯基功能状态评分、全身疾病状态、肿瘤组织学和累积颅内肿瘤体积的多变量模型中,我们观察到,比较1个BM与2 - 10个BM的患者(P < 0.001)或10个BM与>10个BM的患者时,死亡风险增加约10%(P < 0.001)。当将BM数量建模为连续变量而非使用Yamamoto等人的分类方法时,我们观察到每增加6 - 7个BM,死亡风险逐步增加4%(P < 0.001)。
BM数量对总生存期的影响不大,应将其视为SRS和全脑放射治疗决策中众多需考虑的变量之一。