Gaito S, Hwang E J, France A, Aznar M C, Burnet N, Crellin A, Holtzman A L, Indelicato D J, Timmerman B, Whitfield G A, Smith E
Proton Clinical Outcomes Unit, The Christie NHS Proton Beam Therapy Centre, Manchester, UK; Division of Clinical Cancer Science, School of Medical Sciences, The University of Manchester, Manchester, UK.
Department of Proton Beam Therapy, The Christie Proton Beam Therapy Centre, Manchester, UK; Crown Princess Mary Cancer Centre, Westmead Hospital, Sydney, Australia.
Clin Oncol (R Coll Radiol). 2023 May;35(5):283-291. doi: 10.1016/j.clon.2023.01.024. Epub 2023 Feb 9.
In 2008, the UK National Health Service started the Proton Overseas Programme (POP), to provide access for proton beam therapy (PBT) abroad for selected tumour diagnoses while two national centres were being planned. The clinical outcomes for the patient group treated for central nervous system (CNS), base of skull, spinal and paraspinal malignancies are reported here.
Since the start of the POP, an agreement between the National Health Service and UK referring centres ensured outcomes data collection, including overall survival, local tumour control and late toxicity data. Clinical and treatment-related data were extracted from this national patient database. Grade ≥3 late toxicities were reported following Common Terminology Criteria for Adverse Events (CTCAE) v 4.0 definition, occurring later than 90 days since the completion of treatment.
Between 2008 and September 2020, 830 patients were treated within the POP for the above listed malignancies. Overall survival data were available for 815 patients and local control data for 726 patients. Toxicity analysis was carried out on 702 patients, with patients excluded due to short follow-up (<90 days) and/or inadequate toxicity data available. After a median follow-up of 3.34 years (0.06-11.58), the overall survival was 91.2%. The local control rate was 85.9% after a median follow-up of 2.81 years (range 0.04-11.58). The overall grade ≥3 late toxicity incidence was 11.97%, after a median follow-up of 1.72 years (0.04-8.45). The median radiotherapy prescription dose was 54 GyRBE (34.8-79.2).
The results of this study indicate the safety of PBT for CNS tumours. Preliminary clinical outcomes following PBT for paediatric/teen and young adult and adult CNS tumours treated within the POP are encouraging, which reflects accurate patient selection and treatment quality. The rate of late effects compares favourably with published cohorts. Clinical outcomes from this patient cohort will be compared with those of UK-treated patients since the start of the national PBT service in 2018.
2008年,英国国民医疗服务体系启动了质子海外计划(POP),以便在规划两个国家中心期间,为选定的肿瘤诊断患者提供海外质子束治疗(PBT)。本文报告了接受中枢神经系统(CNS)、颅底、脊柱和椎旁恶性肿瘤治疗的患者组的临床结果。
自POP启动以来,国民医疗服务体系与英国转诊中心之间的一项协议确保了结果数据的收集,包括总生存期、局部肿瘤控制和晚期毒性数据。临床和治疗相关数据从这个国家患者数据库中提取。≥3级晚期毒性按照不良事件通用术语标准(CTCAE)v 4.0定义进行报告,发生在治疗完成后90天之后。
2008年至2020年9月期间,830例患者在POP中接受了上述恶性肿瘤的治疗。815例患者有总生存期数据,726例患者有局部控制数据。对702例患者进行了毒性分析,因随访时间短(<90天)和/或可获得的毒性数据不足而排除了部分患者。中位随访3.34年(0.06 - 11.58年)后,总生存率为91.2%。中位随访2.81年(范围0.04 - 11.58年)后,局部控制率为85.9%。中位随访1.72年(0.04 - 8.45年)后,≥3级晚期毒性总发生率为11.97%。中位放射治疗处方剂量为54 GyRBE(34.8 - 79.2)。
本研究结果表明PBT治疗CNS肿瘤的安全性。在POP中接受治疗的儿科/青少年及年轻成人和成人CNS肿瘤患者PBT后的初步临床结果令人鼓舞,这反映了准确的患者选择和治疗质量。晚期效应发生率与已发表队列相比具有优势。该患者队列的临床结果将与自2018年国家PBT服务启动以来在英国接受治疗的患者的结果进行比较。