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首页> 外文期刊>Radiotherapy and oncology: Journal of the European Society for Therapeutic Radiology and Oncology >Acute radiation reactions in oral and pharyngeal mucosa: tolerable levels in altered fractionation schedules.
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Acute radiation reactions in oral and pharyngeal mucosa: tolerable levels in altered fractionation schedules.

机译:口腔和咽粘膜的急性放射反应:分馏方案改变后的可耐受水平。

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摘要

PURPOSE:To investigate whether a predictive estimate can be obtained for a 'tolerance level' of acute oral and pharyngeal mucosal reactions in patients receiving head and neck radiotherapy, using an objective set of dose and time data. MATERIALS AND METHODS:Several dozen radiotherapy schedules for treating head and neck cancer have been reviewed, together with published estimates of whether they were tolerated or (in a number of schedules) not. Those closest to the borderline were given detailed analysis. Total doses and biologically effective doses (BED or ERD) were calculated for a range of starting times of cellular repopulation and rates of daily proliferation. Starting times of proliferation from 5 to 10 days and daily cellular doubling rates of 1-3 days were considered. The standard published form of BED with its linear overall time factor was used: BED=nd(1 + d/(alpha/beta) - Ln2(T - T(k))/alpha T(p) (see text for parameters). RESULTS: A clear progression from acceptable to intolerable mucosal reactions was found, which correlated with total biologically effective dose (BED in our published modeling), for all the head and neck cancer radiotherapy schedules available for study, when ranked into categories of 'intolerable' or 'tolerable'. A review of published mechanisms for mucosal reactions suggested that practical schedules used for treatment caused stimulated compensatory proliferation to start at about 7 days. The starting time of compensatory proliferation had little predictive value in our listing, so we chose the starting time of 7 days. Very short and very long daily doubling rates also had little reliability, so we suggest choosing a doubling time of 2.5 days as a datum. With these parameters a 'tolerance zone of uncertainty' could be identified which predicted acute-reaction acceptability or not of a schedule within a range of about 2-10 Gy in total BED. If concurrent chemoradiotherapy is used, our provisional suggestion is that this zone should be reduced by up to roughly 3-5 Gy10 in BED,with a request for further evidence. CONCLUSIONS:It is suggested that total BED should be used, as specified above. Parameters of alpha=0.35 Gy-(1), alpha/beta=10 Gy, Tk=7 days and Tp=2.5 days are suggested. The 'acute/ tolerance zone' then turns out to be 59-61 Gy10 for radiation-only treatments. Further information about the decrement caused by concurrent head-and-neck cancer chemoradiotherapy, possibly 3-5 Gy10, is required.
机译:目的:使用一组客观的剂量和时间数据,调查是否可以对接受头颈部放疗的患者的急性口腔和咽部粘膜反应的“耐受水平”获得预测性估计。材料和方法:已经审查了几十种用于治疗头颈部癌的放疗方案,以及已发表的关于它们是否可以耐受的估计值(在许多方案中)。对那些最接近边界的人进行了详细分析。计算细胞再填充的起始时间和每日增殖率的总剂量和生物学有效剂量(BED或ERD)。考虑了从5天到10天的增殖开始时间和每天1-3天的细胞倍增速率。使用BED的标准发布形式及其线性总时间因子:BED = nd(1 + d /(alpha / beta)-Ln2(T-T(k))/ alpha T(p)(请参阅参数文字)结果:对于所有可供研究的头颈癌放疗方案,当归类为“不能忍受的”类别时,发现从可接受的黏膜反应到未耐受的黏膜反应有明显的进展,这与总生物有效剂量(在我们已发表的模型中为BED)相关。对已发表的粘膜反应机制的回顾表明,用于治疗的实际时间表导致刺激性代偿性增生开始于约7天,而代偿性增生的开始时间在我们的清单中几乎没有预测价值,因此我们选择了起始时间为7天,非常短和非常长的每日倍增率也几乎没有可靠性,因此我们建议选择2.5天的倍增时间作为基准,使用这些参数可以确定“不确定性的公差范围”预测的急性反应可接受性或计划的总BED约为2-10 Gy。如果同时进行放化疗,我们的临时建议是在BED中将这一区域减少大约3-5 Gy10,并要求进一步的证据。结论:建议应使用总BED,如上所述。建议使用alpha = 0.35 Gy-(1),alpha / beta = 10 Gy,Tk = 7天和Tp = 2.5天的参数。然后,对于仅放射治疗,“急性/耐受区”为59-61 Gy10。需要更多有关并发头颈癌放化疗引起的递减信息,可能为3-5 Gy10。

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