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基于38例患者的额外数据对人类脊髓再照射耐受性的更新。

Update of human spinal cord reirradiation tolerance based on additional data from 38 patients.

作者信息

Nieder Carsten, Grosu Anca L, Andratschke Nicolaus H, Molls Michael

机构信息

Department of Radiation Oncology, Klinikum Rechts der Isar der Technischen Universität München, Munich, Germany.

出版信息

Int J Radiat Oncol Biol Phys. 2006 Dec 1;66(5):1446-9. doi: 10.1016/j.ijrobp.2006.07.1383. Epub 2006 Nov 2.

Abstract

PURPOSE

To update a combined analysis of all published clinical data.

METHODS AND MATERIALS

We collected data from 38 additional patients treated in our department or published in four different reports and calculated the biologically effective dose (BED) according to the linear-quadratic model using an alpha/beta value of 2 Gy for cervical and thoracic cord and 4 Gy for lumbar cord. In this model, a dose of 50 Gy given in single daily fractions of 2 Gy is equivalent to a BED of 100 Gy(2) or 75 Gy(4).

RESULTS

The 2005 risk score based on three variables (cumulative BED, highest BED of all treatment series in a particular individual, and interval), which discriminate three different risk groups, does not require modification. The low-risk group now contains 1 case of radiation myelopathy (RM) after hypofractionated stereotactic reirradiation. Therefore, the rate increased from 0% to 3%. Intermediate-risk patients developed RM in 25%, and high-risk patients in 90%. When the interval between the two treatment courses is not shorter than 6 months and the dose of each course is < or =98 Gy(2), the cumulative BED where no case of RM has yet been reported is 120 Gy(2).

CONCLUSIONS

Based on these updated results, the risk of RM appears small after < or =135.5 Gy(2) when the interval is not shorter than 6 months and the dose of each course is < or =98 Gy(2). We would recommend limiting the dose to the lowest feasible level. The influence of very steep dose gradients from stereotactic and intensity-modulated approaches (i.e., a more complex volume-effect) requires further evaluation.

摘要

目的

更新对所有已发表临床数据的综合分析。

方法和材料

我们收集了在本部门治疗或发表于四份不同报告中的另外38例患者的数据,并根据线性二次模型计算生物等效剂量(BED),颈椎和胸段脊髓的α/β值为2 Gy,腰段脊髓为4 Gy。在此模型中,以每日2 Gy单次分割给予50 Gy的剂量相当于100 Gy(2)或75 Gy(4)的生物等效剂量。

结果

基于三个变量(累积生物等效剂量、特定个体所有治疗系列中的最高生物等效剂量和间隔时间)的2005年风险评分,可区分三个不同风险组,无需修改。低风险组现在有1例在低分割立体定向再照射后发生放射性脊髓病(RM)。因此,发生率从0%增至3%。中风险患者发生RM的比例为25%,高风险患者为90%。当两个疗程之间的间隔不短于6个月且每个疗程的剂量≤98 Gy(2)时,尚未报告RM病例的累积生物等效剂量为120 Gy(2)。

结论

基于这些更新结果,当间隔不短于6个月且每个疗程的剂量≤98 Gy(2)时,生物等效剂量≤135.5 Gy(2)时发生RM的风险似乎较小。我们建议将剂量限制在可行的最低水平。立体定向和调强放疗方法中非常陡峭的剂量梯度的影响(即更复杂的体积效应)需要进一步评估。

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