Mount Vernon Cancer Centre, Northwood, UK; Division of Cancer Sciences, University of Manchester, Manchester, UK.
Cancer Research UK & UCL Cancer Trials Centre, University College London, London, UK.
Lancet Oncol. 2021 Mar;22(3):332-340. doi: 10.1016/S1470-2045(20)30686-0. Epub 2021 Feb 1.
The optimal radiotherapy dose for indolent non-Hodgkin lymphoma is uncertain. We aimed to compare 24 Gy in 12 fractions (representing the standard of care) with 4 Gy in two fractions (low-dose radiation).
FoRT (Follicular Radiotherapy Trial) is a randomised, multicentre, phase 3, non-inferiority trial at 43 study centres in the UK. We enrolled patients (aged >18 years) with indolent non-Hodgkin lymphoma who had histological confirmation of follicular lymphoma or marginal zone lymphoma requiring radical or palliative radiotherapy. No limit on performance status was stipulated, and previous chemotherapy or radiotherapy to another site was permitted. Radiotherapy target sites were randomly allocated (1:1) either 24 Gy in 12 fractions or 4 Gy in two fractions using minimisation and stratified by histology, treatment intent, and study centre. Randomisation was centralised through the Cancer Research UK and University College London Cancer Trials Centre. Patients, treating clinicians, and investigators were not masked to random assignments. The primary endpoint was time to local progression in the irradiated volume based on clinical and radiological evaluation and analysed on an intention-to-treat basis. The non-inferiority threshold aimed to exclude the chance that 4 Gy was more than 10% inferior to 24 Gy in terms of local control at 2 years (HR 1·37). Safety (in terms of adverse events) was analysed in patients who received any radiotherapy and who returned an adverse event form. FoRT is registered with ClinicalTrials.gov, NCT00310167, and the ISRCTN Registry, ISRCTN65687530, and this report represents the long-term follow-up.
Between April 7, 2006, and June 8, 2011, 614 target sites in 548 patients were randomly assigned either 24 Gy in 12 fractions (n=299) or 4 Gy in two fractions (n=315). At a median follow-up of 73·8 months (IQR 61·9-88·0), 117 local progression events were recorded, 27 in the 24 Gy group and 90 in the 4 Gy group. The 2-year local progression-free rate was 94·1% (95% CI 90·6-96·4) after 24 Gy and 79·8% (74·8-83·9) after 4 Gy; corresponding rates at 5 years were 89·9% (85·5-93·1) after 24 Gy and 70·4% (64·7-75·4) after 4 Gy (hazard ratio 3·46, 95% CI 2·25-5·33; p<0·0001). The difference at 2 years remains outside the non-inferiority margin of 10% at -13·0% (95% CI -21·7 to -6·9). The most common events at week 12 were alopecia (19 [7%] of 287 sites with 24 Gy vs six [2%] of 301 sites with 4 Gy), dry mouth (11 [4%] vs five [2%]), fatigue (seven [2%] vs five [2%]), mucositis (seven [2%] vs three [1%]), and pain (seven [2%] vs two [1%]). No treatment-related deaths were reported.
Our findings at 5 years show that the optimal radiotherapy dose for indolent lymphoma is 24 Gy in 12 fractions when durable local control is the aim of treatment.
Cancer Research UK.
惰性非霍奇金淋巴瘤的最佳放疗剂量仍不确定。我们旨在比较 24 Gy 分 12 次(代表标准治疗)与 4 Gy 分 2 次(低剂量放疗)。
FoRT(滤泡性放疗试验)是一项在英国 43 个研究中心进行的随机、多中心、III 期、非劣效性试验。我们招募了需要根治性或姑息性放疗的滤泡性淋巴瘤或边缘区淋巴瘤的惰性非霍奇金淋巴瘤患者(年龄>18 岁)。未规定表现状态的限制,并且允许对另一个部位进行先前的化疗或放疗。使用最小化和分层组织学、治疗意图和研究中心将放疗靶区随机分配(1:1)为 24 Gy 分 12 次或 4 Gy 分 2 次。通过英国癌症研究中心和伦敦大学学院癌症临床试验中心进行中央随机化。患者、治疗医生和研究者对随机分组不知情。主要终点是根据临床和影像学评估照射体积的局部进展时间,按意向治疗进行分析。非劣效性阈值旨在排除 4 Gy 在 2 年时的局部控制率比 24 Gy 低 10%以上的可能性(HR 1.37)。在接受任何放疗并返回不良事件表的患者中分析安全性(不良事件)。FoRT 在 ClinicalTrials.gov、NCT00310167 和 ISRCTN 注册处、ISRCTN65687530 上注册,本报告代表长期随访结果。
2006 年 4 月 7 日至 2011 年 6 月 8 日,548 例患者的 614 个靶区被随机分为 24 Gy 分 12 次(n=299)或 4 Gy 分 2 次(n=315)。在中位随访 73.8 个月(IQR 61.9-88.0)后,记录了 117 例局部进展事件,24 Gy 组 27 例,4 Gy 组 90 例。24 Gy 组 2 年局部无进展率为 94.1%(95%CI 90.6-96.4),4 Gy 组为 79.8%(74.8-83.9);相应的 5 年局部无进展率分别为 89.9%(85.5-93.1)和 70.4%(64.7-75.4)(危险比 3.46,95%CI 2.25-5.33;p<0.0001)。2 年的差异仍在非劣效性边界 10%之外,为-13.0%(95%CI -21.7 至 -6.9)。第 12 周最常见的事件是脱发(24 Gy 组 287 个部位中有 19 个[7%],4 Gy 组 301 个部位中有 6 个[2%])、口干(24 Gy 组 11 个[4%],4 Gy 组 5 个[2%])、疲劳(24 Gy 组 7 个[2%],4 Gy 组 5 个[2%])、黏膜炎(24 Gy 组 7 个[2%],4 Gy 组 3 个[1%])和疼痛(24 Gy 组 7 个[2%],4 Gy 组 2 个[1%])。没有治疗相关的死亡报告。
我们在 5 年的研究结果表明,当以持久的局部控制为治疗目标时,惰性淋巴瘤的最佳放疗剂量为 24 Gy 分 12 次。
英国癌症研究中心。