Department of Radiation Oncology, Cedars-Sinai Medical Center, Los Angeles, California; Department of Radiation Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Boston, Massachusetts.
Department of Radiation Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Boston, Massachusetts.
Pract Radiat Oncol. 2021 Sep-Oct;11(5):e459-e467. doi: 10.1016/j.prro.2020.12.006. Epub 2021 Jan 18.
Patients with locally advanced non-small cell lung cancer (LA-NSCLC) have a high prevalence of pre-existing coronary heart disease and face excess cardiac risk after thoracic radiation therapy. We sought to assess whether statin therapy is a predictor of overall survival (OS) after thoracic radiation therapy.
We performed a retrospective analysis of 748 patients with LA-NSCLC treated with thoracic radiation therapy, using Kaplan-Meier OS estimates and Cox regression.
Statin use among high cardiac risk patients (Framingham risk ≥20% or pre-existing coronary heart disease; n = 496) was 51.2%. After adjustment for baseline cardiac risk and other prognostic factors, statin therapy was associated with a significantly increased risk of all-cause mortality (adjusted hazard ratio, 1.39; 95% confidence interval [CI], 1.00-1.91; P = .048) but not major adverse cardiac events (adjusted hazard ratio, 1.18; 95% CI, 0.52-2.68; P = .69). Among statin-naïve patients, mean heart dose ≥10 Gy versus <10 Gy was associated with a significantly increased risk of all-cause mortality (hazard ratio, 1.32; 95% CI, 1.04-1.68; P = .022), with 2-year OS estimates of 46.9% versus 60.0%, respectively. However, OS did not differ by heart dose among patients on statin therapy (hazard ratio, 1.00; 95% CI, 0.76-1.32; P = 1.00; P-interaction = .031), with 2-year OS estimates of 46.9% versus 50.3%, respectively.
Among patients with LA-NSCLC, only half of statin-eligible high cardiac risk patients were on statin therapy, reflecting the highest cardiac risk level of our cohort. Statin use was an independent predictor of all-cause mortality but not major adverse cardiac events. Elevated mean heart dose (≥10 Gy) was associated with increased risk of all-cause mortality in statin-naïve patients but not among those on statin therapy, identifying a group of patients in which early intervention with statins may mitigate the deleterious effects of high heart radiation therapy dose. This warrants evaluation in prospective trials.
局部晚期非小细胞肺癌(LA-NSCLC)患者普遍存在预先存在的冠心病,并且在接受胸部放射治疗后会面临额外的心脏风险。我们试图评估他汀类药物治疗是否是胸部放射治疗后总生存期(OS)的预测因素。
我们对 748 例接受胸部放射治疗的 LA-NSCLC 患者进行了回顾性分析,使用 Kaplan-Meier OS 估计和 Cox 回归。
高心脏风险患者(Framingham 风险≥20%或预先存在的冠心病;n=496)中他汀类药物的使用率为 51.2%。在调整基线心脏风险和其他预后因素后,他汀类药物治疗与全因死亡率显著增加相关(调整后的危险比,1.39;95%置信区间[CI],1.00-1.91;P=0.048),但与主要不良心脏事件无关(调整后的危险比,1.18;95%CI,0.52-2.68;P=0.69)。在他汀类药物治疗初治患者中,平均心脏剂量≥10Gy 与<10Gy 相比,全因死亡率显著增加(危险比,1.32;95%CI,1.04-1.68;P=0.022),2 年 OS 估计值分别为 46.9%和 60.0%。然而,在接受他汀类药物治疗的患者中,心脏剂量对 OS 没有影响(危险比,1.00;95%CI,0.76-1.32;P=1.00;P 交互=0.031),2 年 OS 估计值分别为 46.9%和 50.3%。
在 LA-NSCLC 患者中,只有一半的他汀类药物适用的高心脏风险患者正在服用他汀类药物,这反映了我们队列的最高心脏风险水平。他汀类药物的使用是全因死亡率的独立预测因素,但不是主要不良心脏事件的预测因素。在他汀类药物治疗初治患者中,平均心脏剂量升高(≥10Gy)与全因死亡率增加相关,但在接受他汀类药物治疗的患者中则不然,这表明在高心脏放射治疗剂量下,早期干预他汀类药物可能减轻其有害影响。这需要在前瞻性试验中进行评估。