Department of Experimental Clinical Oncology, Aarhus University Hospital, Denmark.
Department of Experimental Clinical Oncology, Aarhus University Hospital, Denmark.
Radiother Oncol. 2018 Apr;127(1):12-19. doi: 10.1016/j.radonc.2018.02.018. Epub 2018 Mar 6.
To evaluate if correction of low hemoglobin (Hb) levels by means of darbepoetin alfa improves the outcomes of radiotherapy in patients with squamous cell carcinoma of the head and neck (HNSCC).
Patients eligible for primary radiotherapy and who had Hb values below 14.0 g/dl were randomized to receive accelerated fractionated radiotherapy with or without darbepoetin alfa. Patients also received the hypoxic radiosensitizer nimorazole. Darbepoetin alfa was given weekly during radiotherapy or until the Hb value exceeded 15.5 g/dl.
Following a planned interim analysis which showed inferiority of the experimental treatment the trial was stopped after inclusion of 522 patients (of a planned intake of 600). Of these, 513 were eligible for analysis (254 patients treated with darbepoetin alfa and 259 patients in the control group). Overall, the patients were distributed according to the stratification parameters (gender, T and N staging, tumor site). Treatment with darbepoetin alfa increased the Hb level to the planned value in 81% of the patients. The compliance was good without excess serious adverse events. The results showed a poorer outcome with a 5-year cumulative loco-regional failure rate of 47% vs. 34%, Hazard Ratio (HR): 1.53 [1.16-2.02], for the darbepoetin alfa vs. control arm, respectively. This was also seen for the endpoints of event-free survival (HR: 1.36 [1.09-1.69]), disease-specific death (HR: 1.43 [1.08-1.90]), and overall survival (HR: 1.30 [1.02-1.64]). There was no enhanced risk of cardio-vascular events observed in the experimental arm or any significant differences in acute or late radiation related morbidity. All univariate analyses were confirmed in a multivariate setting.
Correction of the Hb level with darbepoetin alfa during radiotherapy of patients with HNSCC resulted in a significantly poorer tumor control and survival.
评估通过达贝泊汀 α 纠正低血红蛋白(Hb)水平是否能改善头颈部鳞状细胞癌(HNSCC)患者放疗的结局。
符合条件的接受根治性放疗的患者,Hb 值低于 14.0 g/dl,被随机分为接受达贝泊汀 α 治疗或不接受达贝泊汀 α 治疗的加速分割放疗。患者还接受缺氧增敏剂米诺环素。在放疗期间每周给予达贝泊汀 α,直至 Hb 值超过 15.5 g/dl。
在一项计划中的中期分析显示实验组治疗效果较差后,该试验在纳入 600 例患者中的 522 例后停止(计划入组 600 例)。其中 513 例符合分析条件(254 例接受达贝泊汀 α 治疗,259 例对照组)。总体而言,患者根据分层参数(性别、T 和 N 分期、肿瘤部位)分布。达贝泊汀 α 治疗使 81%的患者 Hb 水平达到计划值。依从性良好,无过度严重不良事件。结果显示,实验组 5 年累积局部区域失败率为 47%,而对照组为 34%,风险比(HR)为 1.53(1.16-2.02)。无事件生存(HR:1.36[1.09-1.69])、疾病特异性死亡(HR:1.43[1.08-1.90])和总生存(HR:1.30[1.02-1.64])终点也有类似结果。实验组未观察到心血管事件风险增加,也未观察到急性或晚期放射性相关发病率的显著差异。所有单变量分析均在多变量环境中得到证实。
在 HNSCC 患者放疗期间用达贝泊汀 α 纠正 Hb 水平会显著降低肿瘤控制和生存。