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一种在广泛临床情况下计算重新增殖校正后的肿瘤等效均匀剂量(EQD2)值的通用方法,包括中断治疗的情况。

A generalised method for calculating repopulation-corrected tumour EQD2 values in a wide range of clinical situations, including interrupted treatments.

作者信息

Dale Roger, Plataniotis Georgios, Jones Bleddyn

机构信息

Department of Surgery and Cancer, Faculty of Medicine, Imperial College, London, UK.

Department of Radiation Oncology, Aristoteles University of Thessaloniki, Greece.

出版信息

Phys Med. 2024 Feb;118:103294. doi: 10.1016/j.ejmp.2024.103294. Epub 2024 Jan 9.

Abstract

Any radiotherapy schedule can be characterised by its 2 Gy per fraction equivalent dose (EQD2). EQD2s are easily calculated for late-responding normal tissues but for tumours significant errors may arise if no allowance is made for any repopulation which occurs in the reference and/or the derived EQD2 schedule. This article presents a systematic approach to calculating tumour EQD2 values utilising the concept of biologically effective dose (BED) with inclusion of repopulation effects. A factor (f) is introduced which allows the inter-dependence between EQD2 and its delivery time (and, hence, the amount of repopulation involved) to be embedded within the formulation without any additional assumptions. There exists a transitional BED below which simple methods of calculating tumour EQD2 remain valid. In cases where simpler approaches are inadequate, the correct EQD2 may be determined from the reference schedule BED (BED) by the relationship: EQD2 = A × BED - B, where A and B are constants which involve the same radiobiological parameters as are conventionally used in deriving tumour BED values. Some Worked Examples illustrate application of the method to fractionated radiotherapy and indicate that there can be substantial differences with results obtained from using over-simplified approaches. Since reference BEDs are calculable for other types of radiotherapy (brachytherapy, permanent implants, high-LET applications, etc) the methodology allows estimation of tumour EQD2 values in a wide range of clinical circumstances, including cases which involve interrupted treatments.

摘要

任何放疗方案都可以用其每分次2 Gy等效剂量(EQD2)来表征。对于晚期反应正常组织,EQD2很容易计算,但对于肿瘤,如果在参考和/或推导的EQD2方案中未考虑任何再增殖情况,可能会出现重大误差。本文提出了一种系统方法,利用生物等效剂量(BED)的概念并纳入再增殖效应来计算肿瘤EQD2值。引入了一个因子(f),它能将EQD2与其照射时间之间的相互依赖性(以及因此涉及的再增殖量)纳入公式中,而无需任何额外假设。存在一个过渡性BED,低于此值时,计算肿瘤EQD2的简单方法仍然有效。在简单方法不适用的情况下,可根据参考方案的BED(BED)通过以下关系确定正确的EQD2:EQD2 = A × BED - B,其中A和B是常数,涉及与推导肿瘤BED值时常规使用的相同放射生物学参数。一些实例说明了该方法在分割放疗中的应用,并表明与使用过度简化方法得到的结果可能存在显著差异。由于参考BED可针对其他类型的放疗(近距离放疗、永久性植入、高LET应用等)进行计算,该方法允许在广泛的临床情况下估计肿瘤EQD2值,包括涉及中断治疗的情况。

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