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用于临床前氧引导放射治疗的3D-CRT小鼠剂量描绘研究的回顾性分析与IMRT重新计划

Retrospective analysis and IMRT replanning of a 3D-CRT murine dose painting study for preclinical oxygen-guided radiotherapy.

作者信息

Tummala Rajit, Pearson Erik, Antes Avery, Slagowski Jordan M, Redler Gage, Nilsson Rasmus, Halpern Howard J, Sarigul Neslihan, Ahmed Ibrahim, Velarde Daniela Olivera, Epel Boris, Gertsenshteyn Inna, Aydogan Bulent

机构信息

Department of Radiation and Cellular Oncology and Center for EPR Imaging In Vivo Physiology, The University of Chicago, Chicago, IL, USA.

Department of Human Oncology, University of Wisconsin-Madison, Madison, WI, USA.

出版信息

Sci Rep. 2025 May 22;15(1):17755. doi: 10.1038/s41598-025-01716-6.

Abstract

A recent parallel-opposed 3D-conformal radiotherapy (3D-CRT) study in mice compared dose escalation (boost) in hypoxic (pO2 ≤ 10 torr) and non-hypoxic tumor subvolumes. They found a hypoxic boost led to significantly greater (p < 1e-4) tumor control probability than an equivalent non-hypoxic boost. We imported imaging and treatment data from this study for 31 SCC7 squamous carcinoma murine leg tumor cases-16 hypoxic boost and 15 non-hypoxic boost plans into a commercial treatment planning system for preclinical radiotherapy. Treatments were retrospectively recalculated with a fast Monte Carlo dose engine. We replanned cases with 3-field IMRT using an analogous uncertainty budget as 3D-CRT. Comparing both treatment groups, the hypoxic boost treatments had a significantly higher hypoxic fraction receive the boost prescription as planned in 3D-CRT (p < 1e-4) and IMRT (p < 1e-4). Surprisingly, retrospective 3D-CRT non-hypoxic boost treatments had a significantly lower non-hypoxic fraction receive the boost prescription (p < 1e-4). 3D-CRT non-hypoxic boost also substantially underdosed the entire tumor between 48-68 Gy compared to the "equivalent" hypoxic boost. In IMRT, the non-hypoxic volume receiving boost prescription was significantly higher in the non-hypoxic boost (p = 0.0215) and dosing in the entire tumor was identical between boost groups. This study displays IMRT's potential to advance the quality of preclinical dose painting studies.

摘要

最近一项针对小鼠的平行相对3D适形放疗(3D-CRT)研究比较了缺氧(pO2≤10托)和非缺氧肿瘤亚体积中的剂量递增(加量)情况。他们发现,与同等的非缺氧加量相比,缺氧加量导致肿瘤控制概率显著更高(p<1e-4)。我们将该研究中31例SCC7鳞状细胞癌小鼠腿部肿瘤病例的成像和治疗数据——16例缺氧加量和15例非缺氧加量计划——导入一个用于临床前放疗的商业治疗计划系统。使用快速蒙特卡罗剂量引擎对治疗进行回顾性重新计算。我们使用与3D-CRT类似的不确定性预算,对病例进行了3野IMRT重新计划。比较两个治疗组,缺氧加量治疗中有显著更高比例的缺氧部分按3D-CRT(p<1e-4)和IMRT(p<1e-4)计划接受加量处方。令人惊讶的是,回顾性3D-CRT非缺氧加量治疗中接受加量处方的非缺氧部分显著更低(p<1e-4)。与“等效”的缺氧加量相比,3D-CRT非缺氧加量在48-68 Gy之间也使整个肿瘤剂量明显不足。在IMRT中,接受加量处方的非缺氧体积在非缺氧加量组中显著更高(p=0.0215),并且加量组之间整个肿瘤的剂量相同。这项研究展示了IMRT在提高临床前剂量描绘研究质量方面的潜力。

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