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铅笔束扫描质子治疗儿童神经母细胞瘤,结合运动缓解策略治疗移动靶区。

Pencil Beam Scanning Proton Therapy for Paediatric Neuroblastoma with Motion Mitigation Strategy for Moving Target Volumes.

机构信息

Center for Proton Therapy, Paul Scherrer Institute, Villigen, Switzerland; University College London Hospitals, London, UK.

Center for Proton Therapy, Paul Scherrer Institute, Villigen, Switzerland.

出版信息

Clin Oncol (R Coll Radiol). 2020 Jul;32(7):467-476. doi: 10.1016/j.clon.2020.02.002. Epub 2020 Feb 17.

Abstract

AIMS

More efforts are required to minimise late radiation side-effects for paediatric patients. Pencil beam scanning proton beam therapy (PBS-PT) allows increased sparing of normal tissues while maintaining conformality, but is prone to dose degradation from interplay effects due to respiratory motion. We report our clinical experience of motion mitigation with volumetric rescanning (vRSC) and outcomes of children with neuroblastoma.

MATERIALS AND METHODS

Nineteen patients with high-risk (n = 16) and intermediate-risk (n = 3) neuroblastoma received PBS-PT. The median age at PBS-PT was 3.5 years (range 1.2-8.6) and the median PBS-PT dose was 21 Gy (relative biological effectiveness). Most children (89%) were treated under general anaesthesia. Seven patients (37%) underwent four-dimensional computed tomography for motion assessment and were treated with vRSC for motion mitigation.

RESULTS

The mean result of maximum organ motion was 2.7 mm (cranial-caudal), 1.2 mm (left-right), 1.0 mm (anterior-posterior). Four anaesthetised children (21%) showing <5 mm motion had four-dimensional dose calculations (4DDC) to guide the number of vRSC. The mean deterioration or improvement to the planning target volume covered by 95% of the prescribed dose compared with static three-dimensional plans were: 4DDC no vRSC, -0.6%; 2 vRSC, +0.3%; 4 vRSC, +0.3%; and 8 vRSC, +0.1%. With a median follow-up of 14.9 months (range 2.7-49.0) there were no local recurrences. The 2-year overall survival was 94% and distant progression-free survival was 76%. Acute grade 2-4 toxicity was 11%. During the limited follow-up time, no late toxicities were observed.

CONCLUSIONS

The early outcomes of mainly high-risk patients with neuroblastoma treated with PBS-PT were excellent. With a subset of our cohort undergoing PBS-PT with vRSC we have shown that it is logistically feasible and safe. The clinical relevance of vRSC is debatable in anaesthetised children with small pre-PBS-PT motion of <5 mm.

摘要

目的

需要进一步努力以最小化儿科患者的晚期放射副作用。铅笔束扫描质子束治疗(PBS-PT)允许在保持适形性的同时增加对正常组织的保护,但由于呼吸运动的相互作用,容易导致剂量降低。我们报告了使用容积重扫(vRSC)缓解运动的临床经验以及神经母细胞瘤患儿的治疗结果。

材料和方法

19 例高危(n=16)和中危(n=3)神经母细胞瘤患儿接受了 PBS-PT 治疗。PBS-PT 时的中位年龄为 3.5 岁(范围 1.2-8.6),PBS-PT 剂量的中位值为 21 Gy(相对生物效应)。大多数患儿(89%)在全身麻醉下接受治疗。7 例患儿(37%)进行了四维 CT 运动评估,并接受 vRSC 运动缓解治疗。

结果

最大器官运动的平均结果为 2.7mm(头脚)、1.2mm(左右)、1.0mm(前后)。4 例(21%)麻醉下运动幅度<5mm 的患儿进行了四维剂量计算(4DDC)以指导 vRSC 的次数。与静态三维计划相比,计划靶区 95%覆盖的剂量的平均恶化或改善为:4DDC 无 vRSC,-0.6%;2 次 vRSC,+0.3%;4 次 vRSC,+0.3%;8 次 vRSC,+0.1%。中位随访时间为 14.9 个月(范围 2.7-49.0),无局部复发。2 年总生存率为 94%,远处无进展生存率为 76%。急性 2-4 级毒性为 11%。在有限的随访时间内,未观察到晚期毒性。

结论

主要接受 PBS-PT 治疗的高危神经母细胞瘤患儿的早期结果非常出色。我们的一部分队列患儿接受了 vRSC 的 PBS-PT,结果显示其在操作上是可行且安全的。对于预 PBS-PT 运动幅度<5mm 的麻醉患儿,vRSC 的临床相关性存在争议。

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