State Key Laboratory of Molecular Oncology and Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Division of Biostatistics and Bioinformatics, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Lancet Oncol. 2019 Mar;20(3):352-360. doi: 10.1016/S1470-2045(18)30813-1. Epub 2019 Jan 30.
To our knowledge, no randomised study has compared postmastectomy hypofractionated radiotherapy with conventional fractionated radiotherapy in patients with breast cancer. This study aimed to determine whether a 3-week schedule of postmastectomy hypofractionated radiotherapy is as efficacious and safe as a 5-week schedule of conventional fractionated radiotherapy.
This randomised, non-inferiority, open-label, phase 3 study was done in a single academic hospital in China. Patients aged 18-75 years who had undergone mastectomy and had at least four positive axillary lymph nodes or primary tumour stage T3-4 disease were eligible to participate. Patients were randomly assigned (1:1) according to a computer-generated central randomisation schedule, without stratification, to receive chest wall and nodal irradiation at a dose of 50 Gy in 25 fractions over 5 weeks (conventional fractionated radiotherapy) or 43·5 Gy in 15 fractions over 3 weeks (hypofractionated radiotherapy). The modified intention-to-treat population (including all eligible patients who underwent randomisation but excluding those who were considered ineligible or withdrew consent after randomisation) was used in primary and safety analyses. The primary endpoint was 5-year locoregional recurrence, and a 5% margin was used to establish non-inferiority (equivalent to a hazard ratio <1·883). This trial is registered at ClinicalTrials.gov, number NCT00793962.
Between June 12, 2008, and June 16, 2016, 820 patients were enrolled and randomly assigned to the conventional fractionated radiotherapy group (n=414) or hypofractionated radiotherapy group (n=406). 409 participants in the conventional fractionated radiotherapy group and 401 participants in the hypofractionated radiotherapy group were included in the modified intention-to-treat analyses. At a median follow-up of 58·5 months (IQR 39·2-81·8), 60 (7%) patients had developed locoregional recurrence (31 patients in the hypofractionated radiotherapy group and 29 in the conventional fractionated radiotherapy group); the 5-year cumulative incidence of locoregional recurrence was 8·3% (90% CI 5·8-10·7) in the hypofractionated radiotherapy group and 8·1% (90% CI 5·4-10·6) in the conventional fractionated radiotherapy group (absolute difference 0·2%, 90% CI -3·0 to 2·6; hazard ratio 1·10, 90% CI 0·72 to 1·69; p<0·0001 for non-inferiority). There were no significant differences between the groups in acute and late toxicities, except that fewer patients in the hypofractionated radiotherapy group had grade 3 acute skin toxicity than in the conventional fractionated radiotherapy group (14 [3%] of 401 patients vs 32 [8%] of 409 patients; p<0·0001).
Postmastectomy hypofractionated radiotherapy was non-inferior to and had similar toxicities to conventional fractionated radiotherapy in patients with high-risk breast cancer. Hypofractionated radiotherapy could provide more convenient treatment and allow providers to treat more patients.
National Key Projects of Research and Development of China; the Chinese Academy of Medical Science Innovation Fund for Medical Sciences; and Beijing Marathon of Hope, Cancer Foundation of China.
据我们所知,尚无研究比较乳腺癌患者接受乳房切除术后的短程放疗与常规分割放疗。本研究旨在确定 3 周的乳房切除术后短程放疗方案是否与 5 周常规分割放疗方案同样有效和安全。
这是一项在中国一家单中心学术医院进行的随机、非劣效性、开放标签、3 期研究。年龄 18-75 岁、接受过乳房切除术且至少有 4 个阳性腋窝淋巴结或原发性肿瘤 T3-4 期的患者有资格参与。患者按照中央随机分组方案(1:1)随机分配,不进行分层,接受胸部和淋巴结照射,剂量为 50 Gy,25 次,5 周(常规分割放疗)或 43.5 Gy,15 次,3 周(短程放疗)。使用改良意向治疗人群(包括所有接受随机分组但在随机分组后被认为不符合条件或撤回同意的患者)进行主要和安全性分析。主要终点是 5 年局部区域复发,使用 5%的边缘来确定非劣效性(相当于风险比<1.883)。该试验在 ClinicalTrials.gov 上注册,编号为 NCT00793962。
2008 年 6 月 12 日至 2016 年 6 月 16 日,共纳入 820 例患者,并随机分配至常规分割放疗组(n=414)或短程放疗组(n=406)。常规分割放疗组有 409 名参与者和短程放疗组有 401 名参与者被纳入改良意向治疗分析。中位随访 58.5 个月(IQR 39.2-81.8)时,60(7%)例患者发生局部区域复发(短程放疗组 31 例,常规分割放疗组 29 例);短程放疗组 5 年局部区域复发累积发生率为 8.3%(90%CI 5.8-10.7),常规分割放疗组为 8.1%(90%CI 5.4-10.6)(绝对差值 0.2%,90%CI -3.0 至 2.6;风险比 1.10,90%CI 0.72 至 1.69;p<0.0001 表示非劣效性)。两组间急性和晚期毒性无显著差异,但短程放疗组急性皮肤毒性 3 级的患者少于常规分割放疗组(短程放疗组 401 例中有 14 例[3%],常规分割放疗组 409 例中有 32 例[8%];p<0.0001)。
乳房切除术后短程放疗与常规分割放疗在高危乳腺癌患者中同样有效且毒性相似。短程放疗可以提供更方便的治疗,并允许更多的患者接受治疗。
国家重点研发计划;中国医学科学院医学与健康科技创新工程;中国癌症基金会北京希望马拉松。