Shenouda George, Zhang Qiang, Ang K Kian, Machtay Mitchell, Parliament Matthew B, Hershock Diane, Suntharalingam Mohan, Lin Alexander, Rotman Marvin, Nabid Abdenour, Hong Susan, Shehata Sarwat, Cmelak Anthony J, Sultanem Khalil, Le Quynh-Thu
McGill University, Montreal, Quebec, Canada.
NRG Oncology Statistics and Data Management Center.
Int J Radiat Oncol Biol Phys. 2015 Apr 1;91(5):907-15. doi: 10.1016/j.ijrobp.2014.12.018. Epub 2015 Feb 7.
This paper reports long-term results of RTOG 9903, to determine whether the addition of erythropoietin (EPO) would improve the outcomes of radiation therapy (RT) in mildly to moderately anemic patients with head and neck squamous cell carcinoma (HNSCCa).
The trial included HNSCCa patients treated with definitive RT. Patients with stage III or IV disease received concomitant chemoradiation therapy or accelerated fractionation. Pretreatment hemoglobin levels were required to be between 9.0 and 13.5 g/dL (12.5 g/dL for females). EPO, 40,000 U, was administered weekly starting 7 to 10 days before RT was initiated in the RT + EPO arm.
A total of 141 of 148 enrolled patients were evaluable. The baseline median hemoglobin level was 12.1 g/dL. In the RT + EPO arm, the mean hemoglobin level at 4 weeks increased by 1.66 g/dL, whereas it decreased by 0.24 g/dL in the RT arm. With a median follow-up of 7.95 years (range: 1.66-10.08 years) for surviving patients and 3.33 years for all patients (range: 0.03-10.08 years), the 5-year estimate of local-regional failure was 46.2% versus 39.4% (P=.42), local-regional progression-free survival was 31.5% versus 37.6% (P=.20), and overall survival was 36.9% versus 38.2% (P=.54) for the RT + EPO and RT arms, respectively. Late toxicity was not different between the 2 arms.
This long-term analysis confirmed that despite the ability of EPO to raise hemoglobin levels in anemic patients with HNSCCa, it did not improve outcomes when added to RT. The possibility of a detrimental effect of EPO could not be ruled out.
本文报告了放射肿瘤学组(RTOG)9903试验的长期结果,以确定添加促红细胞生成素(EPO)是否会改善轻度至中度贫血的头颈部鳞状细胞癌(HNSCCa)患者的放射治疗(RT)效果。
该试验纳入了接受根治性放疗的HNSCCa患者。III期或IV期疾病患者接受同步放化疗或加速分割放疗。治疗前血红蛋白水平要求在9.0至13.5g/dL之间(女性为12.5g/dL)。在放疗加EPO组中,从放疗开始前7至10天起,每周给予40,000单位EPO。
148例入组患者中共有141例可评估。基线血红蛋白水平中位数为12.1g/dL。在放疗加EPO组中,4周时平均血红蛋白水平升高了1.66g/dL,而在放疗组中则下降了0.24g/dL。存活患者的中位随访时间为7.95年(范围:1.66 - 10.08年),所有患者的中位随访时间为3.33年(范围:0.03 - 10.08年),放疗加EPO组和放疗组的5年局部区域失败估计率分别为46.2%和39.4%(P = 0.42),局部区域无进展生存率分别为31.5%和37.6%(P = 0.20),总生存率分别为36.9%和38.2%(P = 0.54)。两组的晚期毒性无差异。
这项长期分析证实,尽管EPO能够提高HNSCCa贫血患者的血红蛋白水平,但添加到放疗中并未改善治疗效果。不能排除EPO产生有害影响的可能性。