Department of Oncology, Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark; Danish Centre for Particle Therapy, Aarhus University Hospital, Aarhus, Denmark; Department of Radiation Oncology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Radiother Oncol. 2023 May;182:109526. doi: 10.1016/j.radonc.2023.109526. Epub 2023 Feb 9.
Risk of subclinical disease decreases with increasing distance from the GTV in head- and-neck squamous cell carcinoma (HNSCC). Depending on individual patient anatomy, OAR sparing could be improved by reducing target coverage in regions with low risk of subclinical spread. Using automated multi-criteria optimization, we investigate patient-specific optimal trade-offs between target periphery coverage and OAR sparing.
VMAT plans for 39 HNSCC patients were retrospectively created following our clinical three-target-level protocol: high-risk (PTV1), intermediate-risk (PTV2, 5 mm expansion from PTV1), and elective (PTV3). A baseline plan fulfilling clinical constraints (D 99 % ≥95 % for all PTVs) was compared to three plans with reduced PTV2 coverage (goals: PTV2 D 99 % ≥90 % or 85 %, or no PTV2) at the outer edge of PTV2. Plans were compared on PTV D 99 %, OAR D mean, and NTCP (xerostomia/dysphagia).
Trade-offs between PTV2 coverage and OAR doses varied considerably between patients. For plans with PTV2 D 99 % -goal 90 %, median PTV2 D 99 % was 91.5 % resulting in xerostomia (≥grade 4) and dysphagia (≥grade 2) NTCP decrease of median [maximum] 1.9 % [5.3 %] and 1.1 % [4.1 %], respectively, compared to nominal PTV2 D 99 % -goal 95 %. For PTV2 D 99 % -goal 85 % median PTV D 99 % was 87 % with NTCP improvements of 4.6 % [9.9 %] and 1.5 % [5.4 %]. For no-margin plans, PTV2 D 99 % decreased to 83.3 % with NTCP reductions of 5.1 % [10.2 %] and 1.4 % [6.1 %].
Clinically relevant, patient-specific reductions in OARs and NTCP were observed at limited cost in target under-coverage at the outermost PTV edge. Given the observed inter-patient variations, individual evaluation is warranted to determine whether trade- offs would benefit a specific patient.
在头颈部鳞状细胞癌(HNSCC)中,随着与 GTV 距离的增加,亚临床疾病的风险降低。根据患者个体解剖结构的不同,通过降低低风险亚临床扩散区域的靶区覆盖范围,可以改善 OAR 的保护。使用自动多标准优化,我们研究了靶区边缘覆盖范围和 OAR 保护之间的患者特异性最优权衡。
回顾性地为 39 名 HNSCC 患者创建了 VMAT 计划,这些计划是根据我们的临床三靶区水平方案制定的:高危(PTV1)、中危(PTV2,距 PTV1 扩张 5mm)和选择性(PTV3)。比较了满足临床限制的基准计划(所有 PTV 的 D99%≥95%)与 PTV2 覆盖范围降低的三个计划(目标:PTV2 D99%≥90%或 85%,或 PTV2 无边界)。在 PTV D99%、OAR D 均值和 NTCP(口干/吞咽困难)方面比较了这些计划。
患者之间 PTV2 覆盖范围和 OAR 剂量之间的权衡差异很大。对于 PTV2 D99% -目标 90%的计划,PTV2 D99%的中位数为 91.5%,导致口干(≥4 级)和吞咽困难(≥2 级)的 NTCP 分别降低了中位数[最大值]1.9%[5.3%]和 1.1%[4.1%],与名义 PTV2 D99% -目标 95%相比。对于 PTV2 D99% -目标 85%,PTV D99%的中位数为 87%,NTCP 改善了 4.6%[9.9%]和 1.5%[5.4%]。对于无边界计划,PTV2 D99%降至 83.3%,NTCP 降低了 5.1%[10.2%]和 1.4%[6.1%]。
在外 PTV 边缘的靶区适度覆盖不足的情况下,观察到与临床相关的、患者特异性的 OAR 和 NTCP 减少。鉴于观察到的患者间差异,需要进行个体评估,以确定是否对特定患者有利。