Comparison of Proton Versus Photon SBRT for Treatment of Spinal Metastases Using Variable RBE Models.

IF 2 Q3 ONCOLOGY International Journal of Particle Therapy Pub Date : 2025-03-05 eCollection Date: 2025-06-01 DOI:10.1016/j.ijpt.2025.100743
Sherif G Shaaban, Michael LeCompte, Hao Chen, Daniel Lubelski, Ali Bydon, Nicholas Theodore, Majid Khan, Sang Lee, Khaled Kebaish, Lawrence Kleinberg, Ted Hooker, Heng Li, Kristin J Redmond
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To better understand the safety of proton SBRT for spinal metastasis, this dosimetric analysis compares plans using photon robotic techniques and proton therapy accounting for RBE-weighted dose (D_{RBE}).</p><p><strong>Materials and methods: </strong>Nine patients with spinal metastasis were selected to be representative of a broad range of complex clinical practice (3 cervical, 3 thoracic, 3 lumbar) that are uniquely challenging to treat with SBRT were identified. Each vertebral level contained a case with paraspinal extension, a reirradiation case, and a case with high-grade epidural disease (Bilsky grade ≥1c) given that such complex cases in current practice often require target volume under-coverage with photon SBRT (PH-SBRT) in order to meet organ at risk (OAR) dose constraints. 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Proton plans used the robust optimization parameters of ±3.5% range and 2-mm setup uncertainties. Planning target volume (PTV) coverage and OARs sparing were compared using the Wilcoxon signed-rank test.</p><p><strong>Results: </strong>Planning target volume coverage was significantly improved when comparing PH-SBRT at 30 Gy in 5 fractions (median: 25 Gy) to IMPT at 30 Gy[RBE] in 5 fractions (median: 30.3 Gy[RBE], <i>P</i> = .02) and 45 Gy(RBE) in 5 fractions (median 35.6 Gy[RBE], <i>P</i> = .001). Maximum dose of the spinal cord (cord Dmax) was significantly lower with IMPT at 30 Gy(RBE) (median: 17.6 Gy[RBE], <i>P</i> = .04) and 45 Gy(RBE) (median: 16.1 Gy[RBE], <i>P</i> = .04) compared to conventional plan at 30 Gy (median: 18 Gy). Spinal cord expansion (cord + 2 mm) maximum dose did not change in both photon (median 21.5 Gy) and proton plans (median 22.5, <i>P</i> = .27). Other OARs were better spared with the same and dose-escalated proton plans. 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Abstract

Purpose: Study of proton stereotactic body radiation therapy (SBRT) for spinal metastasis has been limited, largely due to concerns of increased risk of spinal cord injury given the challenges of end of range relative biological effectiveness (RBE). Although the 1.1 RBE constant for proton beam has been adopted for clinical use, data indicate that proton RBE is variable and dependent on technical-, tissue-, and patient factors. To better understand the safety of proton SBRT for spinal metastasis, this dosimetric analysis compares plans using photon robotic techniques and proton therapy accounting for RBE-weighted dose (D_{RBE}).

Materials and methods: Nine patients with spinal metastasis were selected to be representative of a broad range of complex clinical practice (3 cervical, 3 thoracic, 3 lumbar) that are uniquely challenging to treat with SBRT were identified. Each vertebral level contained a case with paraspinal extension, a reirradiation case, and a case with high-grade epidural disease (Bilsky grade ≥1c) given that such complex cases in current practice often require target volume under-coverage with photon SBRT (PH-SBRT) in order to meet organ at risk (OAR) dose constraints. All selected patients were treated with PH-SBRT using a robotic system to a prescription dose of 30 Gy in 5 fractions despite our institutional preference for further dose escalation, because further dose escalation was not feasible in the original planning process while keeping normal tissues below acceptable dose constraints. To see if superior target coverage could be achieved with proton treatment, comparative intensity modulated proton therapy (IMPT) plans were generated with the same prescription dose as what was clinically delivered using the 1.1 RBE constant. Dose escalated IMPT plans were then generated to 45 Gy(RBE) in 5 fractions. Variable RBE models (Carabe, McNamara, and Wedenberg) were then utilized to generate RBE-weighted dose D_{RBE} distribution for 30 Gy(RBE) and 45 Gy(RBE) plans using the α/β value (which was 3.76 in this study), physical dose, linear energy transfer (LET) value, and dose per fraction parameters. Proton plans used the robust optimization parameters of ±3.5% range and 2-mm setup uncertainties. Planning target volume (PTV) coverage and OARs sparing were compared using the Wilcoxon signed-rank test.

Results: Planning target volume coverage was significantly improved when comparing PH-SBRT at 30 Gy in 5 fractions (median: 25 Gy) to IMPT at 30 Gy[RBE] in 5 fractions (median: 30.3 Gy[RBE], P = .02) and 45 Gy(RBE) in 5 fractions (median 35.6 Gy[RBE], P = .001). Maximum dose of the spinal cord (cord Dmax) was significantly lower with IMPT at 30 Gy(RBE) (median: 17.6 Gy[RBE], P = .04) and 45 Gy(RBE) (median: 16.1 Gy[RBE], P = .04) compared to conventional plan at 30 Gy (median: 18 Gy). Spinal cord expansion (cord + 2 mm) maximum dose did not change in both photon (median 21.5 Gy) and proton plans (median 22.5, P = .27). Other OARs were better spared with the same and dose-escalated proton plans. No difference was seen in cord Dmax when comparing the PH-SBRT at 30 Gy to D_{RBE} at 30 and 45 Gy(RBE) using Carabe-, McNamara-, or Wedenberg models. However, for spinal cord expansion (cord + 2 mm), there was significant difference between PH-SBRT and D_{RBE} at 30 Gy(RBE) and 45 Gy(RBE) in 5 fractions using Carabe- (median: 25.4 Gy[RBE], P = .002), McNamara- (median: 25.1 Gy[RBE], P = .003), or Wedenberg (median: 24.8 Gy[RBE], P = .0001) models. The average increase in the spinal cord expansion maximum dose using these models compared to the fixed RBE plans was 5.3%.

Conclusion: We report the first dosimetric analysis of proton SBRT for spine metastasis using variable RBE dose models. Compared to photon SBRT, IMPT may provide improved target coverage and better spare adjacent OARs, though fixed RBE models can underestimate the maximum dose to adjacent OARs. Future prospective studies are needed to validate these results.

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使用可变RBE模型比较质子与光子SBRT治疗脊柱转移瘤。
目的:质子立体定向体放射治疗(SBRT)治疗脊柱转移的研究一直受到限制,主要是因为考虑到范围内相对生物有效性(RBE)的挑战,担心会增加脊髓损伤的风险。虽然质子束的1.1 RBE常数已被用于临床应用,但数据表明质子RBE是可变的,依赖于技术、组织和患者因素。为了更好地了解质子SBRT治疗脊柱转移的安全性,本剂量学分析比较了使用光子机器人技术和质子治疗方案的RBE加权剂量(D_{RBE})。材料和方法:选择9例脊柱转移患者,以代表广泛的复杂临床实践(3例颈椎,3例胸椎,3例腰椎),确定采用SBRT治疗具有独特挑战性。每个椎节段包含一个椎旁延伸病例,一个再照射病例和一个高级别硬膜外疾病病例(Bilsky分级≥1c),因为在目前的实践中,这些复杂的病例通常需要光子SBRT (PH-SBRT)覆盖下的靶体积,以满足器官危险(OAR)剂量限制。所有选定的患者都使用机器人系统接受PH-SBRT治疗,处方剂量为30 Gy,分5份,尽管我们的机构倾向于进一步增加剂量,因为在最初的计划过程中,进一步增加剂量是不可行的,同时保持正常组织低于可接受的剂量限制。为了观察质子治疗是否能达到更好的目标覆盖率,我们制定了比较强度调制质子治疗(IMPT)计划,其处方剂量与临床使用1.1 RBE常数给予的剂量相同。然后将剂量递增的IMPT计划分成5份,达到45 Gy(RBE)。然后利用可变RBE模型(Carabe、McNamara和Wedenberg),利用α/β值(本研究为3.76)、物理剂量、线性能量转移(LET)值和每组分剂量参数,生成30 Gy(RBE)和45 Gy(RBE)方案的RBE加权剂量D_{RBE}分布。质子方案采用了±3.5%范围和2mm设置不确定度的稳健优化参数。计划目标体积(PTV)覆盖率和桨叶节约使用Wilcoxon符号秩检验进行比较。结果:PH-SBRT为30 Gy分5次组(中位数为25 Gy), IMPT为30 Gy[RBE]分5次组(中位数为30.3 Gy[RBE], P = 0.02), IMPT为45 Gy(RBE)分5次组(中位数为35.6 Gy[RBE], P = 0.001),计划靶体积覆盖率显著提高。IMPT在30 Gy(RBE)(中位数:17.6 Gy[RBE], P = .04)和45 Gy(RBE)(中位数:16.1 Gy[RBE], P = .04)时脊髓最大剂量(脊髓Dmax)显著低于常规计划在30 Gy(中位数:18 Gy)。在光子计划(中位21.5 Gy)和质子计划(中位22.5 Gy, P = 0.27)中,脊髓扩张(脊髓+ 2mm)的最大剂量没有变化。其他桨更好地幸免于相同和剂量递增的质子计划。使用Carabe-、McNamara-或Wedenberg模型比较30 Gy时的PH-SBRT与30和45 Gy(RBE)时的Dmax没有差异。然而,对于脊髓扩张(脊髓+ 2毫米),使用Carabe-(中位数:25.4 Gy[RBE], P = 0.003), McNamara-(中位数:25.1 Gy[RBE], P = 0.003)或Wedenberg(中位数:24.8 Gy[RBE], P = 0.0001)模型,PH-SBRT和D_{RBE}在30 Gy(RBE)和45 Gy(RBE)的5个分数之间存在显著差异。与固定RBE计划相比,使用这些模型的脊髓扩张最大剂量平均增加5.3%。结论:我们首次报道了采用可变RBE剂量模型对质子SBRT治疗脊柱转移的剂量学分析。与光子SBRT相比,IMPT可以提供更好的目标覆盖和更好的备用相邻桨,尽管固定RBE模型可能低估了相邻桨的最大剂量。需要进一步的前瞻性研究来验证这些结果。
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来源期刊
International Journal of Particle Therapy
International Journal of Particle Therapy Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
3.70
自引率
5.90%
发文量
23
审稿时长
20 weeks
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