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基于体素的剂量不均匀性定量在接受 90Y-依替膦单抗替伊莫单抗治疗的患者中的应用。

Quantification of dose nonuniformities by voxel-based dosimetry in patients receiving 90Y-ibritumomab-tiuxetan.

机构信息

Nuclear Medicine, Department of Translational Medicine, Faculty of Medicine and Psychology, Sant'Andrea Hospital, Sapienza University of Rome, Rome, Italy.

出版信息

Cancer Biother Radiopharm. 2013 Mar;28(2):98-107. doi: 10.1089/cbr.2012.1299. Epub 2013 Jan 4.

Abstract

UNLABELLED

Abstract Objective: To assess the impact of nonuniform dose distribution within lesions and tumor-involved organs of patients receiving Zevalin(®), and to discuss possible implications of equivalent uniform biological effective doses (EU-BED) on treatment efficacy and toxicity. MATLAB™ -based software for voxel-based dosimetry was adopted for this purpose.

METHODS

Eleven lesions from seven patients with either indolent or aggressive non-Hodgkin lymphoma were analyzed, along with four organs with disease. Absorbed doses were estimated by a direct integration of single-voxel kinetic data from serial tomographic images. After proper corrections, differential BED distributions and surviving cell fractions were estimated, allowing for the calculation of EU-BED. To quantify dose uniformity in each target area, a heterogeneity index was defined.

RESULTS

Average doses were below those prescribed by conventional radiotherapy to eradicate lymphoma lesions. Dose heterogeneity and effect on tumor control varied among lesions, with no apparent relation to tumor mass. Although radiation doses to involved organs were safe, unexpected liver toxicity occurred in one patient who presented with a pattern of diffuse infiltration.

CONCLUSION

Voxel-based dosimetry and radiobiologic modeling can be successfully applied to lesions and tumor-involved organs, representing a methodological advance over estimation of mean absorbed doses. However, effects on tumor control and organ toxicity still cannot be easily predicted.

摘要

目的

评估接受 Zevalin(®)治疗的患者病变和肿瘤累及器官内不均匀剂量分布的影响,并讨论等效均匀生物有效剂量(EU-BED)对治疗效果和毒性的可能影响。采用基于 MATLAB™的体素剂量计算软件进行了此项研究。

方法

分析了 7 名惰性或侵袭性非霍奇金淋巴瘤患者的 11 个病变和 4 个患病器官,通过对连续断层图像的单个体素动力学数据进行直接积分来估计吸收剂量。经过适当的校正,估计了不同的 BED 分布和存活细胞分数,从而计算出 EU-BED。为了量化每个靶区的剂量均匀性,定义了一个不均匀性指数。

结果

平均剂量低于传统放疗消除淋巴瘤病变所需的剂量。病变之间的剂量不均匀性和对肿瘤控制的影响各不相同,与肿瘤质量无明显关系。尽管受累器官的辐射剂量是安全的,但在一名表现为弥漫性浸润的患者中出现了意外的肝毒性。

结论

体素剂量计算和放射生物学建模可成功应用于病变和肿瘤累及器官,这代表了一种比估计平均吸收剂量更先进的方法。然而,对肿瘤控制和器官毒性的影响仍然难以预测。

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