Cummings Bernard, Keane Thomas, Pintilie Melania, Warde Padraig, Waldron John, Payne David, Liu Fei-Fei, Bissett Randy, McLean Michael, Gullane Patrick, O'Sullivan Brian
Department of Radiation Oncology, Princess Margaret Hospital, University of Toronto, Ontario, Canada.
Radiother Oncol. 2007 Oct;85(1):7-16. doi: 10.1016/j.radonc.2007.09.010.
Fractionation strategies delivered over 4 weeks are of clinical and radiobiological interest because treatment is completed before radiotherapy (RT) induced clonogen proliferation commences in earnest approximately 3 to 4 weeks into a course of RT. We wished to test the clinical hypothesis that an increased total dose delivered over 4 weeks with smaller than standard doses per fraction in locally advanced squamous cell carcinoma (SCC) may result in relative protection of late responding tissues and an increased tumor control compared to a conventional daily course in the same overall time.
Between 1988 and 1995 a randomized controlled trial employing RT alone was undertaken at the Princess Margaret Hospital that included 331 eligible patients with T3 or T4 N0 or any N-positive oropharynx, hypopharynx, or larynx primary SCC. RT was randomly assigned to one of two 4 week schedules, either 51 Gy in 20 equal daily fractions, termed conventional fractionation (CF), or 58 Gy in 40 equal fractions given twice per day as a hyperfractionated (HF) experimental arm.
The 5-year local relapse rate was reduced in the HF (41%) compared to the CF arm (49%). This difference was marginally not significant (p=0.082) when the effect was not adjusted. When the effect of the treatment was adjusted by Cox model for clinical factors that included N-category, ECOG performance status, site of disease, T-category, age, hemoglobin, and gender the HF achieved a significant effect (p=0.02). Survival (40% vs. 30%) was also improved with HF compared to CF arm. This difference was only marginally not significant (p=0.069) but again achieved statistical significance when the model was adjusted for clinical factors (p=0.01). Similar results were observed for disease free survival. Although reversible acute toxicity was increased with HF, the overall 5-year rate of grade 3 and 4 late toxicity for the CF was 10.5% compared to 7.7% in the higher dose HF arm.
HF delivered in 4 weeks permits enhanced RT doses achieving improved tumor control, without increased late toxicity, compared to daily fractionated radiotherapy in the same overall time.
为期4周的分割放疗策略具有临床和放射生物学意义,因为在放疗(RT)疗程约3至4周放疗诱导的克隆原增殖真正开始之前,治疗就已完成。我们希望验证这样一个临床假设:与相同总时长的常规每日疗程相比,在局部晚期鳞状细胞癌(SCC)中,4周内给予增加的总剂量且每次分割剂量小于标准剂量,可能会相对保护晚期反应组织并提高肿瘤控制率。
1988年至1995年间,玛格丽特公主医院开展了一项仅采用放疗的随机对照试验,纳入了331例符合条件的T3或T4 N0或任何N阳性的口咽、下咽或喉原发性SCC患者。放疗被随机分配到两个4周方案之一,要么是20次每日等剂量分割给予51 Gy,称为常规分割(CF),要么是40次等剂量分割给予58 Gy,每天两次,作为超分割(HF)试验组。
与CF组(49%)相比,HF组(41%)的5年局部复发率降低。未调整效应时,这种差异略无统计学意义(p = 0.082)。当通过Cox模型针对包括N分期、ECOG体能状态、疾病部位、T分期、年龄、血红蛋白和性别等临床因素调整治疗效应时,HF组有显著效果(p = 0.02)。与CF组相比,HF组的生存率(40%对30%)也有所提高。这种差异同样略无统计学意义(p = 0.069),但在针对临床因素调整模型后再次达到统计学显著性(p = 0.01)。无病生存率也观察到类似结果。虽然HF组可逆性急性毒性增加,但CF组5年3级和4级晚期毒性的总体发生率为10.5%,而较高剂量HF组为7.7%。
与相同总时长的每日分割放疗相比,4周内进行的超分割放疗允许增加放疗剂量,实现更好的肿瘤控制,且不增加晚期毒性。