Department of Therapeutic Radiology, Yale School of Medicine, New Haven, Connecticut.
21st Century Oncology, Fort Myers, Florida.
Int J Radiat Oncol Biol Phys. 2016 Dec 1;96(5):1011-1020. doi: 10.1016/j.ijrobp.2016.08.033. Epub 2016 Aug 31.
To determine the effect of biologically effective dose (BED) and radiation treatment schedule on overall survival (OS) in patients with early-stage non-small cell lung cancer (NSCLC) undergoing stereotactic body radiation therapy (SBRT).
Using data from 65 treatment centers in the United States, we retrospectively reviewed the records of T1-2 N0 NSCLC patients undergoing SBRT alone from 2006 to 2014. Biologically relevant covariates, including dose per fraction, number of fractions, and time between fractions, were used to quantify BED and radiation treatment schedule. The linear-quadratic equation was used to calculate BED and to generate a dichotomous dose variable of <105 Gy versus ≥105 Gy BED. The primary outcome was OS. We used the Kaplan-Meier method, the log-rank test, and Cox proportional hazards regression with propensity score matching to determine whether prescription BED was associated with OS.
We identified 747 patients who met inclusion criteria. The median BED was 132 Gy, and 59 (7.7%) had consecutive-day fractions. Median follow-up was 41 months, and 452 patients (60.5%) had died by the conclusion of the study. The 581 patients receiving ≥105 Gy BED had a median survival of 28 months, whereas the 166 patients receiving <105 Gy BED had a median survival of 22 months (log-rank, P=.01). Radiation treatment schedule was not a significant predictor of OS on univariable analysis. After adjusting for T stage, sex, tumor histology, and Eastern Cooperative Oncology Group performance status, BED ≥105 Gy versus <105 Gy remained significantly associated with improved OS (hazard ratio 0.78, 95% confidence interval 0.62-0.98, P=.03). Propensity score matching on imbalanced variables within high- and low-dose cohorts confirmed a survival benefit with higher prescription dose.
We found that dose escalation to 105 Gy BED and beyond may improve survival in NSCLC patients treated with SBRT.
确定生物有效剂量(BED)和放疗方案对接受立体定向体部放疗(SBRT)的早期非小细胞肺癌(NSCLC)患者总生存期(OS)的影响。
我们使用来自美国 65 个治疗中心的数据,回顾性分析了 2006 年至 2014 年期间单独接受 SBRT 的 T1-2 N0 NSCLC 患者的记录。使用与生物相关的协变量,包括剂量分割、分割次数和分割间隔,来量化 BED 和放疗方案。使用线性二次方程计算 BED,并生成<105Gy 与≥105Gy BED 的二分类剂量变量。主要结局为 OS。我们使用 Kaplan-Meier 法、对数秩检验和 Cox 比例风险回归与倾向评分匹配来确定处方 BED 是否与 OS 相关。
我们确定了 747 名符合纳入标准的患者。中位 BED 为 132Gy,59 例(7.7%)采用连续日分割。中位随访时间为 41 个月,研究结束时 452 例(60.5%)患者死亡。接受≥105Gy BED 的 581 例患者中位生存期为 28 个月,而接受<105Gy BED 的 166 例患者中位生存期为 22 个月(对数秩检验,P=.01)。放疗方案在单变量分析中不是 OS 的显著预测因素。在校正 T 分期、性别、肿瘤组织学和东部肿瘤协作组表现状态后,BED≥105Gy 与<105Gy 相比仍与 OS 改善显著相关(风险比 0.78,95%置信区间 0.62-0.98,P=.03)。在高剂量和低剂量队列中对不平衡变量进行倾向评分匹配证实了较高处方剂量的生存获益。
我们发现,BED 剂量递增至 105Gy 及以上可能会改善接受 SBRT 的 NSCLC 患者的生存。