Hydrogel and scalp/skin conductivities impact dose from tumor treating fields.

IF 4.3 3区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Frontiers in Bioengineering and Biotechnology Pub Date : 2025-02-24 eCollection Date: 2025-01-01 DOI:10.3389/fbioe.2025.1484317
Edwin Lok, Olivia Liang, Monika Haack, Eric T Wong
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引用次数: 0

Abstract

Purpose: Tumor Treating Fields (TTFields) are delivered by transducer arrays applied to scalp or body surface for treatment of multiple malignancies. Dermatologic complications are thought to be related to hydrogel situated between the electrodes and scalp or skin to facilitate electric field penetration. High intensity of TTFields on these surfaces may also be a contributing factor. We explored conductivity changes in the hydrogel and skin to improve TTFields coverage and penetration.

Methods: Magnetic resonance imaging datasets from 12 glioblastoma patients and attenuation-corrected positron emission tomography-computed tomography datasets from 3 non-small cell lung and 2 ovarian carcinoma patients were used to segment anatomic structures. Finite element mesh models were generated and solved for distribution of applied electric fields, rate of energy deposition, and current density at the gross tumor volume (GTV) and clinical target volume (CTV). Electric field-volume, specific absorption rate-volume, and current density-volume histograms were generated, by which plan quality metrics were used to evaluate relative differences in field coverage between models at various hydrogel and skin conductivities.

Results: By varying conductivity of hydrogel, TTFields coverage at GTV or CTV increased up to 0.5 S/m for head and 1.0 S/m for thorax and pelvis models, and no additional increase was observed beyond these saturation points. Although scalp hotspots increased or decreased by +1.5%, -0.1%, and -0.9% in E5%, SAR5%, and CD5%, the skin hotspots increased by as much as +23.5%, +45.7%, and +20.6%, respectively. When altering conductivity of the entire scalp, TTFields coverage peaked near 1 S/m at the GTV or CTV for the head models. TTFields coverage in both the GTV and scalp increased up to 1 S/m for the head models but plateaued thereafter. Contouring under the scalp increased scalp hotspots by +316% in E5% at 1 S/m compared to altering the conductivity of the entire scalp. GTV hotspots decreased by +17% in E5% at 1 S/m.

Conclusion: TTFields delivery can be modulated by the conductivity of hydrogel and scalp/skin at the transducer-scalp or transducer-skin interface. Optimizing this aspect of TTFields delivery may increase tumor control while minimizing toxicity at the scalp or skin.

目的:肿瘤治疗场(TTFields)是通过应用于头皮或体表的换能器阵列产生的,用于治疗多种恶性肿瘤。皮肤并发症被认为与电极和头皮或皮肤之间的水凝胶有关,以促进电场穿透。这些表面上的高强度 TTFields 也可能是一个诱因。我们探索了水凝胶和皮肤的导电性变化,以改善 TTFields 的覆盖和穿透:我们使用 12 名胶质母细胞瘤患者的磁共振成像数据集以及 3 名非小细胞肺癌患者和 2 名卵巢癌患者的衰减校正正电子发射断层扫描数据集来分割解剖结构。生成了有限元网格模型,并对应用电场的分布、能量沉积率以及肿瘤总体积(GTV)和临床靶体积(CTV)的电流密度进行了求解。生成了电场-体积、比吸收率-体积和电流密度-体积直方图,通过这些直方图,计划质量指标被用来评估不同水凝胶和皮肤电导率下模型间电场覆盖范围的相对差异:通过改变水凝胶的电导率,TTFields 在 GTV 或 CTV 的覆盖率在头部增加到 0.5 S/m,在胸部和骨盆模型增加到 1.0 S/m,超过这些饱和点后没有观察到额外的增加。虽然头皮热点在 E5%、SAR5% 和 CD5% 中分别增加或减少了 +1.5%、-0.1% 和 -0.9%,但皮肤热点却分别增加了高达 +23.5%、+45.7% 和 +20.6%。当改变整个头皮的电导率时,TTFields 的覆盖范围在头部模型的 GTV 或 CTV 处达到接近 1 S/m 的峰值。头部模型的 GTV 和头皮的 TTFields 覆盖率都增加到 1 S/m,但随后趋于平稳。与改变整个头皮的电导率相比,在 1 S/m 时,头皮下的轮廓使 E5% 的头皮热点增加了 +316%。在1 S/m的E5%中,GTV热点减少了+17%:结论:水凝胶和头皮/皮肤在换能器-头皮或换能器-皮肤界面的电导率可调节 TTFields 输送。优化 TTFields 输送的这一环节可提高肿瘤控制率,同时将头皮或皮肤的毒性降至最低。
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来源期刊
Frontiers in Bioengineering and Biotechnology
Frontiers in Bioengineering and Biotechnology Chemical Engineering-Bioengineering
CiteScore
8.30
自引率
5.30%
发文量
2270
审稿时长
12 weeks
期刊介绍: The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs. In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.
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