Office of New Drug V, Pharmaceuticals and Medical Devices Agency, Tokyo, Japan.
Office of Medical Devices I, Pharmaceuticals and Medical Devices Agency, Tokyo, Japan.
Oncologist. 2021 Jul;26(7):e1250-e1255. doi: 10.1002/onco.13805. Epub 2021 May 18.
The Japanese Ministry of Health, Labour and Welfare approved a drug called borofalan ( B), a treatment system, and a dose calculation program for boron neutron capture therapy (BNCT) in March 2020. The application pertaining to the products submitted to the Pharmaceuticals and Medical Devices Agency was supported by a Japanese, open-label, uncontrolled trial (Study 002) in patients with unresectable, locally recurrent head and neck squamous cell carcinoma after chemoradiotherapy or radiotherapy, or in those with unresectable locally advanced or locally recurrent (LA/LR) head and neck nonsquamous cell carcinoma. The drug was administered as a single intravenous dose using infusion rates of 200 mg/kg per hour for the first 2 hours after the start of administration and 100 mg/kg per hour during irradiation. Neutron irradiation was performed using the devices at a single dose of 12 Gy-equivalent for oral, pharyngeal, or laryngeal mucosa for up to 60 minutes from 2 hours after the start of drug administration. The primary endpoint was the overall response rate (ORR). The results of Study 002 showed that the ORR based on an assessment of the Independent Central Review Committee per RECIST version 1.1 was 71.4% (90% confidence interval [CI], 51.3%-86.8%). The lower limit of the 90% CI exceeded the prespecified threshold for ORR. When BNCT is applied to patients with unresectable LA/LR head and neck cancer, precautions should be taken, and patients should be monitored for possible onset of dysphagia, brain abscess, skin disorder, crystal urine, cataract, and/or carotid hemorrhage. IMPLICATIONS FOR PRACTICE: Borofalan ( B), a treatment system and a dose calculation program for boron neutron capture therapy (BNCT), demonstrated significant efficacy in an open-label, uncontrolled trial in which overall response rate was the primary endpoint for patients with unresectable locally advanced or locally recurrent head and neck cancer. Although no information about survival benefits was obtained, BNCT will become an effective treatment option that is expected to manage local lesions that are intractable with any standard therapy. In addition, BNCT is expected to maintain quality of life of the intended patient population, on account of its high tumor selectivity and low invasiveness.
2020 年 3 月,日本厚生劳动省批准了一种名为硼替佐米(B)的药物、硼中子俘获治疗(BNCT)的治疗系统和剂量计算程序。向药品医疗器械局提交的产品申请得到了一项日本、开放性、非对照试验(Study 002)的支持,该试验入组了经放化疗后不可切除的局部复发性头颈部鳞状细胞癌,或不可切除的局部晚期或局部复发性(LA/LR)头颈部非鳞状细胞癌患者。药物以静脉输注的方式给药,首 2 小时输注速率为 200mg/kg/小时,然后输注速率为 100mg/kg/小时,同时进行照射。照射使用设备进行,单次剂量为 12Gy 等效剂量,从给药开始后 2 小时起,持续 60 分钟,照射范围为口腔、咽或喉黏膜。主要终点为总缓解率(ORR)。Study 002 的结果显示,根据独立中心审查委员会(IRC)基于 RECIST 版本 1.1 的评估,ORR 为 71.4%(90%置信区间[CI]:51.3%-86.8%)。90%CI 的下限超过了 ORR 的预设阈值。当 BNCT 应用于不可切除的 LA/LR 头颈部癌症患者时,应注意预防,并监测可能发生的吞咽困难、脑脓肿、皮肤疾病、结晶尿、白内障和/或颈动脉出血。临床意义:硼替佐米(B)是一种硼中子俘获治疗(BNCT)的治疗系统和剂量计算程序,在一项开放性、非对照试验中显示出显著疗效,该试验的主要终点为不可切除的局部晚期或局部复发性头颈部癌症患者的总缓解率。虽然没有获得关于生存获益的信息,但 BNCT 将成为一种有效的治疗选择,有望治疗任何标准治疗都无法控制的局部病变。此外,由于 BNCT 具有高度的肿瘤选择性和低侵袭性,预计将维持目标患者人群的生活质量。