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用于碳离子治疗的 RBE 加权剂量模型评估:迈向 HIT 临床实践的现代化:在体、在体和在患者中。

Assessment of RBE-Weighted Dose Models for Carbon Ion Therapy Toward Modernization of Clinical Practice at HIT: In Vitro, in Vivo, and in Patients.

机构信息

Clinical Cooperation Unit Translational Radiation Oncology, National Center for Tumor Diseases, Heidelberg University Hospital and German Cancer Research Center, Heidelberg, Germany; Division of Molecular and Translational Radiation Oncology, Department of Radiation Oncology, Heidelberg Faculty of Medicine and Heidelberg University Hospital, Heidelberg Ion-Beam Therapy Center, Heidelberg, Germany; German Cancer Consortium Core-Center Heidelberg, German Cancer Research Center, Heidelberg, Germany; Clinical Cooperation Unit Radiation Oncology, Heidelberg Institute of Radiation Oncology, National Center for Radiation Oncology, Heidelberg University and German Cancer Research Center, Heidelberg, Germany; Faculty of Physics and Astronomy, Heidelberg University, Germany.

Clinical Cooperation Unit Translational Radiation Oncology, National Center for Tumor Diseases, Heidelberg University Hospital and German Cancer Research Center, Heidelberg, Germany; Division of Molecular and Translational Radiation Oncology, Department of Radiation Oncology, Heidelberg Faculty of Medicine and Heidelberg University Hospital, Heidelberg Ion-Beam Therapy Center, Heidelberg, Germany; German Cancer Consortium Core-Center Heidelberg, German Cancer Research Center, Heidelberg, Germany; Clinical Cooperation Unit Radiation Oncology, Heidelberg Institute of Radiation Oncology, National Center for Radiation Oncology, Heidelberg University and German Cancer Research Center, Heidelberg, Germany; Faculty of Biosciences, Heidelberg University, Germany.

出版信息

Int J Radiat Oncol Biol Phys. 2020 Nov 1;108(3):779-791. doi: 10.1016/j.ijrobp.2020.05.041. Epub 2020 Jun 3.

DOI:10.1016/j.ijrobp.2020.05.041
PMID:32504659
Abstract

PURPOSE

Present-day treatment planning in carbon ion therapy is conducted with assumptions for a limited number of tissue types and models for effective dose. Here, we comprehensively assess relative biological effectiveness (RBE) in carbon ion therapy and associated models toward the modernization of current clinical practice in effective dose calculation.

METHODS

Using 2 human (A549, H460) and 2 mouse (B16, Renca) tumor cell lines, clonogenic cell survival assay was performed for examination of changes in RBE along the full range of clinical-like spread-out Bragg peak (SOBP) fields. Prediction power of the local effect model (LEM1 and LEM4) and the modified microdosimetric kinetic model (mMKM) was assessed. Experimentation and analysis were carried out in the frame of a multidimensional end point study for clinically relevant ranges of physical dose (D), dose-averaged linear energy transfer (LET), and base-line photon radio-sensitivity (α/β). Additionally, predictions were compared against previously reported RBE measurements in vivo and surveyed in patient cases.

RESULTS

RBE model prediction performance varied among the investigated perspectives, with mMKM prediction exhibiting superior agreement with measurements both in vitro and in vivo across the 3 investigated end points. LEM1 and LEM4 performed their best in the highest LET conditions but yielded overestimations and underestimations in low/midrange LET conditions, respectively, as demonstrated by comparison with measurements. Additionally, the analysis of patient treatment plans revealed substantial variability across the investigated models (±20%-30% uncertainty), largely dependent on the selected model and absolute values for input tissue parameters α and β.

CONCLUSION

RBE dependencies in vitro, in vivo, and in silico were investigated with respect to various clinically relevant end points in the context of tumor-specific tissue radio-sensitivity assignment and accurate RBE modeling. Discovered model trends and performances advocate upgrading current treatment planning schemes in carbon ion therapy and call for verification via clinical outcome analysis with large patient cohorts.

摘要

目的

目前在碳离子治疗中进行的治疗计划是基于对有限数量的组织类型和有效剂量模型的假设。在这里,我们全面评估了碳离子治疗中的相对生物效应(RBE)以及与有效剂量计算的当前临床实践现代化相关的模型。

方法

使用 2 个人类(A549、H460)和 2 个小鼠(B16、Renca)肿瘤细胞系,进行集落形成细胞存活测定,以检查 RBE 在整个临床样扩展布拉格峰(SOBP)场范围内的变化。评估了局部效应模型(LEM1 和 LEM4)和修正的微剂量动力学模型(mMKM)的预测能力。实验和分析是在多维终点研究的框架内进行的,涉及临床相关的物理剂量(D)、剂量平均线性能量传递(LET)和基线光子放射敏感性(α/β)范围。此外,还将预测结果与之前报道的体内 RBE 测量值进行了比较,并对患者病例进行了调查。

结果

RBE 模型的预测性能因所研究的角度而异,mMKM 预测在 3 个研究终点上,无论是在体内还是在体外,都与测量值具有更好的一致性。LEM1 和 LEM4 在最高 LET 条件下表现最佳,但在低/中 LET 条件下分别产生高估和低估,如与测量值的比较所示。此外,对患者治疗计划的分析表明,在所研究的模型之间存在很大的变异性(±20%-30%的不确定性),主要取决于所选模型和输入组织参数α和β的绝对值。

结论

在考虑肿瘤特异性组织放射敏感性分配和准确 RBE 建模的情况下,针对各种临床相关终点,研究了体外、体内和体内的 RBE 依赖性。发现的模型趋势和性能支持在碳离子治疗中升级当前的治疗计划方案,并呼吁通过大型患者队列的临床结果分析进行验证。

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