A Review of Proton Therapy - Current Status and Future Directions.

Q4 Medicine Precision Radiation Oncology Pub Date : 2022-06-01 Epub Date: 2022-04-27 DOI:10.1002/pro6.1149
Radhe Mohan
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There is emerging evidence that the resulting sparing of the immune system has the potential to improve outcomes. Protons, accelerated to therapeutic energies ranging from 70 to 250 MeV, are transported to the treatment room where they enter the treatment head mounted on a rotating gantry. The initially narrow beams of protons are spread laterally and longitudinally and shaped appropriately to deliver treatments. Spreading and shaping can be achieved by electro-mechanically for \"passively-scattered proton therapy' (PSPT); or using magnetic scanning of thin \"beamlets\" of protons of a sequence of initial energies. The latter technique is used to treat patients with optimized intensity modulated proton therapy (IMPT), the most powerful proton therapy modality, which is rapidly supplanting PSPT. Treatment planning and plan evaluation for proton therapy require different techniques compared to photon therapy due, in part, to the greater vulnerability of protons to uncertainties, especially those introduced by inter- and intra-fractional variations in anatomy. In addition to anatomic variations, other sources of uncertainty in the treatments delivered include the approximations and assumptions of models used for computing dose distributions and the current practice of proton therapy of assuming the RBE to have a constant value of 1.1. In reality, the RBE is variable and a complex function of proton energy, dose per fraction, tissue and cell type, end point, etc. Despite the high theoretical potential of proton therapy, the clinical evidence supporting its broad use has so far been mixed. The uncertainties and approximations mentioned above, and the technological limitations of proton therapy may have diminished its true clinical potential. 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Abstract

The original rationale for proton therapy was the highly conformal depth-dose distributions that protons are able to produce, compared to photons, which allow greater sparing of normal tissues and escalation of tumor doses, thus potentially improving outcomes. Additionally, recent research, which is still ongoing, has revealed previously unrecognized advantages of proton therapy. For instance, the higher relative biological effectiveness (RBE) near the end of the proton range can be exploited to increase the difference in biologically effective dose in tumors vs. normal tissues. Moreover, the smaller "dose bath", i.e., the compact nature of proton dose distributions has been found to reduce exposure of circulating lymphocytes and the immune organs at risk. There is emerging evidence that the resulting sparing of the immune system has the potential to improve outcomes. Protons, accelerated to therapeutic energies ranging from 70 to 250 MeV, are transported to the treatment room where they enter the treatment head mounted on a rotating gantry. The initially narrow beams of protons are spread laterally and longitudinally and shaped appropriately to deliver treatments. Spreading and shaping can be achieved by electro-mechanically for "passively-scattered proton therapy' (PSPT); or using magnetic scanning of thin "beamlets" of protons of a sequence of initial energies. The latter technique is used to treat patients with optimized intensity modulated proton therapy (IMPT), the most powerful proton therapy modality, which is rapidly supplanting PSPT. Treatment planning and plan evaluation for proton therapy require different techniques compared to photon therapy due, in part, to the greater vulnerability of protons to uncertainties, especially those introduced by inter- and intra-fractional variations in anatomy. In addition to anatomic variations, other sources of uncertainty in the treatments delivered include the approximations and assumptions of models used for computing dose distributions and the current practice of proton therapy of assuming the RBE to have a constant value of 1.1. In reality, the RBE is variable and a complex function of proton energy, dose per fraction, tissue and cell type, end point, etc. Despite the high theoretical potential of proton therapy, the clinical evidence supporting its broad use has so far been mixed. The uncertainties and approximations mentioned above, and the technological limitations of proton therapy may have diminished its true clinical potential. It is generally acknowledged that proton therapy is safe, effective and recommended for many types of pediatric cancers, ocular melanomas, chordomas and chondrosarcomas. Promising results have been and continue to be reported for many other types of cancers as well; however, they are based on small studies. At the same time, there have been reports of unforeseen toxicities. Furthermore, because of the high cost of establishing and operating proton therapy centers, questions are often raised about the value of proton therapy. The general consensus is that there is a need for continued improvement in the state of the art of proton therapy. There is also a need to conduct randomized trials and/or collect outcomes data in multi-institutional registries to generate high level evidence of the advantages of protons. Fortuitously, such efforts are taking currently place. Ongoing research is aimed at better understanding the biological and immunomodulatory effects of proton therapy and the consequences of the physical uncertainties on proton therapy and reducing them through image-guidance and adaptive radiotherapy. Since residual uncertainties will remain despite our best efforts, in order to increase the resilience of dose distributions in the face of uncertainties and improve our confidence in dose distributions seen on treatment plans, robust optimization techniques are being developed and implemented and continue to be perfected. Such research and continuing technological advancements in planning and delivery methods are likely to help demonstrate the superiority of protons.

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质子疗法回顾--现状与未来方向。
质子疗法的最初理论依据是,与光子相比,质子能够产生高度保形的深度-剂量分布,从而能够更大程度地保护正常组织和增加肿瘤剂量,从而有可能改善治疗效果。此外,最近的研究(仍在进行中)发现了质子疗法以前未曾认识到的优势。例如,可以利用质子范围末端较高的相对生物有效性(RBE)来增加肿瘤与正常组织的生物有效剂量差异。此外,较小的 "剂量浴",即质子剂量分布的紧凑性,已被发现可减少循环淋巴细胞和免疫器官的暴露风险。越来越多的证据表明,由此产生的对免疫系统的保护有可能改善治疗效果。加速到 70 到 250 兆电子伏治疗能量的质子被输送到治疗室,进入安装在旋转龙门上的治疗头。最初很窄的质子束会横向和纵向扩散,并进行适当的整形,以进行治疗。在 "被动散射质子疗法"(PSPT)中,散射和塑形可以通过电子机械来实现;或者使用磁力扫描初始能量序列的薄质子 "小束"。后一种技术用于对患者进行优化强度调制质子治疗(IMPT),这是一种最强大的质子治疗模式,正在迅速取代被动散射质子治疗。与光子疗法相比,质子疗法的治疗计划和计划评估需要不同的技术,部分原因是质子更容易受到不确定性的影响,尤其是解剖结构的分段间和分段内变化所带来的不确定性。除了解剖结构的变化外,治疗效果的其他不确定因素还包括用于计算剂量分布的模型的近似值和假设,以及质子疗法目前假设 RBE 为 1.1 的恒定值的做法。实际上,RBE 是可变的,是质子能量、单位剂量、组织和细胞类型、终点等的复杂函数。尽管质子疗法具有很高的理论潜力,但迄今为止支持其广泛应用的临床证据却参差不齐。上文提到的不确定性和近似性,以及质子疗法的技术局限性可能削弱了其真正的临床潜力。人们普遍认为,质子疗法安全、有效,建议用于多种类型的儿童癌症、眼部黑色素瘤、脊索瘤和软骨肉瘤。对于许多其他类型的癌症,质子疗法也取得了可喜的成果,但这些成果都是基于小规模的研究。与此同时,也有关于意外毒性的报道。此外,由于建立和运营质子治疗中心的成本高昂,人们经常对质子治疗的价值提出质疑。人们普遍认为,质子疗法的技术水平需要不断提高。此外,还需要进行随机试验和/或在多机构登记中收集结果数据,以获得质子优势的高水平证据。幸运的是,这些工作目前正在进行中。正在进行的研究旨在更好地了解质子疗法的生物和免疫调节作用,以及物理不确定性对质子疗法的影响,并通过图像引导和自适应放疗来减少这些影响。尽管我们尽了最大努力,但残余的不确定性依然存在,因此,为了增强剂量分布在不确定性面前的弹性,提高我们对治疗计划中剂量分布的信心,我们正在开发和实施稳健的优化技术,并将继续加以完善。这些研究以及计划和给药方法方面的持续技术进步很可能有助于证明质子的优越性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Precision Radiation Oncology
Precision Radiation Oncology Medicine-Oncology
CiteScore
1.20
自引率
0.00%
发文量
32
审稿时长
13 weeks
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