低剂量中度低分割放疗治疗惰性非霍奇金淋巴瘤:一项多中心、单臂、2期试验

Xin-Yue Wang,Xi-Mei Zhang,Liang Wang,Lin-Rui Gao,Ke Chen,Xiao-Li Feng,Wei Rao,Rong Zheng,Yun-Peng Wu,Yong-Wen Song,Hui Fang,Bo Chen,Jing Jin,Yue-Ping Liu,Hao Jing,Yuan Tang,Wen-Wen Zhang,Yi-Rui Zhai,Ning-Ning Lu,Ning Li,Chang-Fa Xia,Shu-Lian Wang,Xin Liu,Ye-Xiong Li,Shu-Nan Qi
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引用次数: 0

摘要

背景:惰性非霍奇金淋巴瘤的放射治疗已经发展到优化最终剂量,同时最小化毒性。我们的目的是评估12 Gy低剂量放疗方案在惰性非霍奇金淋巴瘤患者中的活性和安全性。方法:这项多中心、单臂、2期试验研究纳入了来自中国4家医院的患者。新诊断或复发的I-IV期惰性非霍奇金淋巴瘤(滤泡性淋巴瘤、边缘区淋巴瘤和低级别淋巴瘤),年龄在18岁或以上,东部肿瘤合作组表现状态为0-3的患者符合条件。患者接受受累部位放疗,剂量为12 Gy,分为四部分。主要终点是放疗后6个月的完全缓解率。所有分析均在意向治疗人群中进行。该试验已在ClinicalTrials.gov注册,注册号为NCT05543070,由于COVID-19大流行而延迟了4个月;招聘已完成,后续工作正在进行中。结果:在2022年5月8日至2023年11月8日期间,纳入71例患者(73个靶点)(中位年龄55岁[IQR 48-65];男性29人[41%],女性42人[59%];而且都是亚洲人)。中位随访19个月(IQR 16-22), 6个月完全缓解率为95% (95% CI 87-98;73个地点中的69个)。最常见的急性不良事件是1级淋巴细胞减少(71例患者中有20例[28%])和1级恶心(73例患者中有14例[19%])。唯一的3级或以上不良事件是3级淋巴细胞减少(71例患者中有8例[11%])。未发现与治疗相关的死亡。结论:12 Gy四组分的治疗方案是安全的,并且作为无痛性非霍奇金淋巴瘤患者的局部治疗显示出有希望的活性。鉴于该试验的回顾性注册,有必要进一步研究评估该策略的有效性。中国医学科学院医学科学创新基金、国家高水平医院临床研究基金、中国癌症基金会北京希望跑专项基金。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low-dose moderate hypofractionated radiotherapy for indolent non-Hodgkin lymphoma: a multicentre, single-arm, phase 2 trial.
BACKGROUND Radiotherapy for indolent non-Hodgkin lymphoma has evolved to optimise the definitive dose while minimising toxicity. We aimed to assess the activity and safety of a hypofractionated low-dose radiotherapy regimen of 12 Gy in four fractions in patients with indolent non-Hodgkin lymphoma. METHODS This multicentre, single-arm, phase 2 trial study enrolled patients from four hospitals in China. Patients aged 18 years or older with newly diagnosed or relapsed stage I-IV indolent non-Hodgkin lymphoma (follicular lymphoma, marginal zone lymphoma, and low-grade lymphoma) and an Eastern Cooperative Oncology Group performance status of 0-3 were eligible. Patients underwent involved-site radiotherapy at a dose of 12 Gy in four fractions. The primary endpoint was the complete response rate 6 months after radiotherapy. All analyses were performed in the intention-to-treat population. This trial was registered with ClinicalTrials.gov, NCT05543070, with a four-month delay due to the COVID-19 pandemic; recruitment is complete and follow-up is ongoing. FINDINGS Between May 8, 2022, and Nov 8, 2023, 71 patients (with 73 target sites) were enrolled (median age 55 years [IQR 48-65]; 29 [41%] male and 42 [59%] female; and all were Asian). With a median follow-up of 19 months (IQR 16-22), the 6-month complete response was 95% (95% CI 87-98; 69 of 73 sites). The most common acute adverse events were grade 1 lymphopenia (20 [28%] of 71 patients) and grade 1 nausea (14 [19%] of 73 sites). The sole grade 3 or higher adverse event was grade 3 lymphopenia (eight [11%] of 71 patients). No treatment-related deaths were noted. INTERPRETATION The regimen of 12 Gy in four fractions is safe and shows promising activity as a local treatment for patients with indolent non-Hodgkin lymphoma. Given the retrospective registration of the trial, further studies evaluating the efficacy of this strategy are warranted. FUNDING The Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences, the National High Level Hospital Clinical Research Funding, and the Beijing Hope Run Special Fund of Cancer Foundation of China.
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