Department of Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Department of Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Int J Radiat Oncol Biol Phys. 2017 May 1;98(1):131-141. doi: 10.1016/j.ijrobp.2017.01.201. Epub 2017 Jan 26.
Prior statistical models attempted to identify risk factors for time to distant brain failure (DBF) or time to salvage whole-brain radiation therapy (WBRT) to predict the benefit of early WBRT versus stereotactic radiosurgery (SRS) alone. We introduce a novel clinical metric, brain metastasis velocity (BMV), for predicting clinical outcomes after initial DBF following upfront SRS alone.
BMV was defined as the cumulative number of new brain metastases that developed over time since first SRS in years. Patients were classified by BMV into low-, intermediate-, and high-risk groups, consisting of <4, 4 to 13, and >13 new metastases per year, respectively. Histology, number of metastases at the time of first SRS, and systemic disease status were assessed for effect on BMV.
Of 737 patients treated at our institution with upfront SRS without WBRT, 286 had ≥1 DBF event. A lower BMV predicted for improved overall survival (OS) following initial DBF (log-rank P<.0001). Median OS for the low, intermediate, and high BMV groups was 12.4 months (95% confidence interval [CI], 10.4-16.9 months), 8.2 months (95% CI, 5.0-9.7 months), and 4.3 months (95% CI, 2.6-6.7 months), respectively. Multivariate analysis showed that BMV remained the dominant predictor of OS, with a hazard ratio of 2.75 for the high BMV group (95% CI, 1.94-3.89; P<.0001) and a hazard ratio of 1.65 for the intermediate BMV group (95% CI, 1.18-2.30; P<.004). A lower BMV was associated with decreased rates of salvage WBRT (P=.02) and neurologic death (P=.008). Factors predictive for a higher BMV included ≥2 initial brain metastases (P=.004) and melanoma histology (P=.008).
BMV is a novel metric associated with OS, neurologic death, and need for salvage WBRT after initial DBF following upfront SRS alone.
先前的统计模型试图确定远处脑失败(DBF)或挽救全脑放射治疗(WBRT)时间的风险因素,以预测早期 WBRT 相对于单独立体定向放射外科(SRS)的益处。我们引入了一种新的临床指标,脑转移速度(BMV),用于预测单独进行初始 SRS 后首次 DBF 后的临床结果。
BMV 定义为自首次 SRS 以来每年新发生的脑转移的累积数量。患者根据 BMV 分为低危、中危和高危组,分别为每年<4、4 至 13 和>13 个新转移灶。评估了组织学、首次 SRS 时的转移灶数量和全身疾病状态对 BMV 的影响。
在我院接受单独 upfront SRS 而未接受 WBRT 治疗的 737 例患者中,有 286 例发生≥1 次 DBF 事件。较低的 BMV 预测初始 DBF 后总生存期(OS)改善(对数秩 P<.0001)。低、中、高 BMV 组的中位 OS 分别为 12.4 个月(95%置信区间 [CI],10.4-16.9 个月)、8.2 个月(95% CI,5.0-9.7 个月)和 4.3 个月(95% CI,2.6-6.7 个月)。多变量分析显示,BMV 仍然是 OS 的主要预测因素,高 BMV 组的危险比为 2.75(95% CI,1.94-3.89;P<.0001),中 BMV 组的危险比为 1.65(95% CI,1.18-2.30;P<.004)。较低的 BMV 与降低挽救性 WBRT 率(P=.02)和神经死亡率(P=.008)相关。较高 BMV 的预测因素包括≥2 个初始脑转移灶(P=.004)和黑色素瘤组织学(P=.008)。
BMV 是一种与 OS、神经死亡和单独进行初始 SRS 后首次 DBF 后需要挽救性 WBRT 相关的新指标。