Extreme protraction for low-grade gliomas: theoretical proof of concept of a novel therapeutical strategy

Victor M. Pérez-García;Luis A. Pérez-Romasanta
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引用次数: 2

Abstract

Grade II gliomas are slowly growing primary brain tumours that affect mostly young patients and become fatal after a variable time period. Current clinical handling includes surgery as first-line treatment. Cytotoxic therapies (radiotherapy RT or chemotherapy QT) are used initially only for patients having a bad prognosis. Therapies are administered following the ‘maximum dose in minimum time’ principle, which is the same schedule used for high-grade brain tumours. Using mathematical models describing the growth of these tumours in response to radiotherapy, we find that an extreme protraction therapeutical strategy, i.e. enlarging substantially the time interval between RT fractions, may lead to better tumour control. Explicit formulas are found providing the optimal spacing between doses in a very good agreement with the simulations of the full 3D mathematical model approximating the tumour spatiotemporal dynamics. This idea, although breaking the well-established paradigm, has biological meaning since, in these slowly growing tumours, it may be more favourable to treat the tumour as the tumour cells leave the quiescent compartment and move into the cell cycle.
低级别胶质瘤的极端延长:一种新的治疗策略概念的理论证明
II级胶质瘤是一种生长缓慢的原发性脑肿瘤,主要影响年轻患者,并在不同的时期后变得致命。目前的临床处理包括手术作为一线治疗。细胞毒性治疗(放疗、RT或化疗QT)最初仅用于预后不良的患者。治疗遵循“最短时间内最大剂量”的原则,这与用于治疗高级别脑肿瘤的计划相同。使用数学模型描述这些肿瘤对放疗的反应,我们发现一个极端的延长治疗策略,即大幅扩大RT分数之间的时间间隔,可能会导致更好的肿瘤控制。明确的公式提供了剂量之间的最佳间隔,与模拟接近肿瘤时空动力学的完整3D数学模型非常吻合。这一观点虽然打破了公认的范式,但具有生物学意义,因为在这些生长缓慢的肿瘤中,当肿瘤细胞离开静止腔室进入细胞周期时,治疗肿瘤可能更有利。
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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