Department of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, USA.
Department of Radiation Oncology, University of California Los Angeles, USA.
Radiother Oncol. 2020 Jul;148:235-242. doi: 10.1016/j.radonc.2020.04.037. Epub 2020 Apr 28.
To characterize the efficacy (5-year disease-free survival [DFS]) and safety (incidence of grade 2+ late gastrointestinal or genitourinary toxicity) of ultrahypofractionated radiation therapy (UHRT) versus hypofractionated radiation therapy (HFRT) and conventionally fractionated radiation therapy (CFRT) by comparing patients treated on phase III protocols.
A PICOS/PRISMA/MOOSE protocol was used to identify eligible studies. Weighted random effects meta-analyses were conducted using the DerSimonian and Laird method. Wald-type tests were used to compare treatment modalities for each outcome, where the null hypothesis was rejected for p < 0.05.
Seven studies were included that consisted of 6795 patients (2849 CFRT, 3357 HFRT, and 589 UHRT). Median age was 68 years. Summary effect sizes for 5-year DFS were 85.1% (95% CI: 82.1%-87.8%) for CFRT, 86% (95% CI: 83%-88.7%) for HFRT, and 85% (95% CI: 80%-87%) for UHRT (p = 0.66 and p = 0.8 for CFRT vs. HFRT and CFRT versus UHRT, respectively). Summary effect sizes for late grade 2+ gastrointestinal toxicity were 12.1% (95% CI: 9.2%-15.4%) for CFRT, 14.6% (95% CI: 9.9%-20%) for HFRT, and 10% (95% CI: 7%-13%) for UHRT (p = 0.41 and p = 0.09 for CFRT versus HFRT and CFRT versusus UHRT, respectively). Summary effect sizes for late grade 2+ genitourinary toxicity were 19.4% (95% CI: 10.7-29.9%) for CFRT, 20.4% (95% CI: 10.2%-32.9%) for HFRT, and 18% (95% CI: 15%-22%) for UHRT (p = 0.89 and p = 0.92 for CFRT versus HFRT and CFRT versus UHRT, respectively).
Ultrahypofrationated regimens appear to offer similar levels of safety and efficacy to CFRT and HFRT. These findings are hypothesis-generating and require further validation by ongoing prospective trials.
通过比较接受 III 期方案治疗的患者,描述超分割放疗(UHRT)与分割放疗(HFRT)和常规分割放疗(CFRT)的疗效(5 年无病生存率[DFS])和安全性(2 级及以上晚期胃肠道或泌尿生殖系统毒性发生率)。
采用 PICOS/PRISMA/MOOSE 方案,检索合格研究。使用 DerSimonian 和 Laird 方法进行加权随机效应荟萃分析。采用 Wald 型检验比较每种结局的治疗方式,当 p<0.05 时,拒绝零假设。
共纳入 7 项研究,共纳入 6795 例患者(CFRT 2849 例、HFRT 3357 例、UHRT 589 例)。中位年龄为 68 岁。CFRT、HFRT 和 UHRT 的 5 年 DFS 汇总效应大小分别为 85.1%(95%CI:82.1%-87.8%)、86%(95%CI:83%-88.7%)和 85%(95%CI:80%-87%)(p=0.66 和 p=0.8,分别为 CFRT 与 HFRT 以及 CFRT 与 UHRT 比较)。CFRT、HFRT 和 UHRT 的晚期 2 级及以上胃肠道毒性汇总效应大小分别为 12.1%(95%CI:9.2%-15.4%)、14.6%(95%CI:9.9%-20%)和 10%(95%CI:7%-13%)(p=0.41 和 p=0.09,分别为 CFRT 与 HFRT 以及 CFRT 与 UHRT 比较)。CFRT、HFRT 和 UHRT 的晚期 2 级及以上泌尿生殖系统毒性汇总效应大小分别为 19.4%(95%CI:10.7-29.9%)、20.4%(95%CI:10.2%-32.9%)和 18%(95%CI:15%-22%)(p=0.89 和 p=0.92,分别为 CFRT 与 HFRT 以及 CFRT 与 UHRT 比较)。
超分割方案似乎与 CFRT 和 HFRT 具有相似的安全性和疗效。这些发现只是提出了假设,需要通过正在进行的前瞻性试验进一步验证。