McTyre Emory R, Johnson Adam G, Ruiz Jimmy, Isom Scott, Lucas John T, Hinson William H, Watabe Kounosuke, Laxton Adrian W, Tatter Stephen B, Chan Michael D
Department of Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Department of Medicine (Hematology & Oncology), Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Neuro Oncol. 2017 Apr 1;19(4):558-566. doi: 10.1093/neuonc/now184.
In this study we attempted to discern the factors predictive of neurologic death in patients with brain metastasis treated with upfront stereotactic radiosurgery (SRS) without whole brain radiation therapy (WBRT) while accounting for the competing risk of nonneurologic death.
We performed a retrospective single-institution analysis of patients with brain metastasis treated with upfront SRS without WBRT. Competing risks analysis was performed to estimate the subdistribution hazard ratios (HRs) for neurologic and nonneurologic death for predictor variables of interest.
Of 738 patients treated with upfront SRS alone, neurologic death occurred in 226 (30.6%), while nonneurologic death occurred in 309 (41.9%). Multivariate competing risks analysis identified an increased hazard of neurologic death associated with diagnosis-specific graded prognostic assessment (DS-GPA) ≤ 2 (P = .005), melanoma histology (P = .009), and increased number of brain metastases (P<.001), while there was a decreased hazard associated with higher SRS dose (P = .004). Targeted agents were associated with a decreased HR of neurologic death in the first 1.5 years (P = .04) but not afterwards. An increased hazard of nonneurologic death was seen with increasing age (P =.03), nonmelanoma histology (P<.001), presence of extracranial disease (P<.001), and progressive systemic disease (P =.004).
Melanoma, DS-GPA, number of brain metastases, and SRS dose are predictive of neurologic death, while age, nonmelanoma histology, and more advanced systemic disease are predictive of nonneurologic death. Targeted agents appear to delay neurologic death.
在本研究中,我们试图识别接受 upfront 立体定向放射外科治疗(SRS)而未接受全脑放疗(WBRT)的脑转移患者中预测神经学死亡的因素,同时考虑非神经学死亡的竞争风险。
我们对接受 upfront SRS 且未接受 WBRT 的脑转移患者进行了单机构回顾性分析。进行竞争风险分析以估计感兴趣的预测变量的神经学和非神经学死亡的亚分布风险比(HRs)。
在仅接受 upfront SRS 治疗的 738 例患者中,226 例(30.6%)发生神经学死亡,309 例(41.9%)发生非神经学死亡。多变量竞争风险分析确定,与特定诊断分级预后评估(DS-GPA)≤2(P = 0.005)、黑色素瘤组织学(P = 0.009)和脑转移瘤数量增加(P<0.001)相关的神经学死亡风险增加,而与更高的 SRS 剂量相关的风险降低(P = 0.004)。靶向药物在前 1.5 年与神经学死亡的 HR 降低相关(P = 0.04),但之后则不然。随着年龄增加(P = 0.03)、非黑色素瘤组织学(P<0.001)、存在颅外疾病(P<0.001)和进行性全身疾病(P = 0.004),非神经学死亡风险增加。
黑色素瘤、DS-GPA、脑转移瘤数量和 SRS 剂量可预测神经学死亡,而年龄、非黑色素瘤组织学和更晚期的全身疾病可预测非神经学死亡。靶向药物似乎可延迟神经学死亡。