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克隆源性细胞的预处理数量及其放射敏感性是分次照射后局部肿瘤控制的主要决定因素。

Pre-treatment number of clonogenic cells and their radiosensitivity are major determinants of local tumour control after fractionated irradiation.

作者信息

Yaromina Ala, Krause Marie, Thames Howard, Rosner Andrea, Krause Mechthild, Hessel Franziska, Grenman Reidar, Zips Daniel, Baumann Michael

机构信息

OncoRay - Centre for Radiation Research in Oncology, University of Technology Dresden, Germany.

出版信息

Radiother Oncol. 2007 Jun;83(3):304-10. doi: 10.1016/j.radonc.2007.04.020. Epub 2007 May 22.

Abstract

OBJECTIVE

The response of tumours to fractionated radiotherapy is determined by many factors including repopulation, reoxygenation, the number of clonogenic cells, and their intrinsic radiosensitivity. However, after single radiation doses given under conditions of clamp hypoxia, the dose to control a tumour locally is dependent only on the number of clonogenic cells and their cellular radiosensitivity. Therefore, these parameters were investigated using local control after single doses given under hypoxia, to predict the outcome of fractionated irradiation.

MATERIALS AND METHODS

Ten hSCC cell lines (FaDu, UT-SCC-15, UT-SCC-14, XF354, UT-SCC-5, UT-SCC-45, SAS, CAL-33, UT-SCC-8, and HSC-4) were transplanted subcutaneously into the right hind-leg of NMRI nude mice. At 7mm in diameter, tumours were irradiated either with graded single doses under clamp blood flow conditions (n=873) or with 30 graded fractions within 6 weeks (n=905) under ambient conditions. Local tumour control was determined 120 days after irradiation. Radiation response was quantified in terms of TCD(50), i.e. the dose required to control 50% of tumours locally.

RESULTS

Ten tumour lines investigated showed a pronounced heterogeneity in both TCD(50(30fx/6w)) after fractionated irradiation and TCD(50(SDclamp)) after single dose irradiation. TCD(50(30fx/6w)) varied between 45Gy for UT-SCC-45 and 127Gy for SAS; TCD(50(SDclamp)) varied between 42Gy for UT-SCC-14 and 66Gy for CAL-33. Two tumours were excluded from further analysis due to immunogenicity or non-defined TCD(50). Linear regression analysis revealed a significant positive correlation between TCD(50(SDclamp)) and TCD(50(30fx/6w)) (R(2)=0.82, p=0.002).

CONCLUSIONS

Significant association between TCD(50(SDclamp)) and TCD(50(30fx/6w)) suggests that the pre-treatment number of clonogenic tumour cells and their cellular radiosensitivity have a major impact on local control after fractionated radiotherapy.

摘要

目的

肿瘤对分割放疗的反应由多种因素决定,包括再增殖、再氧合、克隆源性细胞数量及其内在放射敏感性。然而,在钳夹缺氧条件下给予单次辐射剂量后,局部控制肿瘤所需的剂量仅取决于克隆源性细胞的数量及其细胞放射敏感性。因此,利用缺氧条件下单次剂量后的局部控制情况来研究这些参数,以预测分割照射的结果。

材料与方法

将10种人鳞状细胞癌(hSCC)细胞系(FaDu、UT-SCC-15、UT-SCC-14、XF354、UT-SCC-5、UT-SCC-45、SAS、CAL-33、UT-SCC-8和HSC-4)皮下移植到NMRI裸鼠的右后肢。当肿瘤直径达到7mm时,在钳夹血流条件下用分级单次剂量照射(n = 873),或在环境条件下于6周内用30次分级分割照射(n = 905)。照射后120天确定局部肿瘤控制情况。根据肿瘤局部控制率(TCD)(50)对放射反应进行量化,即局部控制50%肿瘤所需的剂量。

结果

所研究的10种肿瘤细胞系在分割照射后的TCD(50(30fx/6w))和单次剂量照射后的TCD(50(SD钳夹))方面均表现出明显的异质性。TCD(50(30fx/6w))在UT-SCC-45为45Gy至SAS为127Gy之间变化;TCD((50(SD钳夹))在UT-SCC-14为42Gy至CAL-33为66Gy之间变化。由于免疫原性或未明确的TCD(50),排除了2个肿瘤用于进一步分析。线性回归分析显示TCD(50(SD钳夹))与TCD(50(30fx/6w))之间存在显著正相关(R² = 0.82,p = 0.002)。

结论

TCD(50(SD钳夹))与TCD(50(30fx/6w))之间的显著关联表明,克隆源性肿瘤细胞的预处理数量及其细胞放射敏感性对分割放疗后的局部控制有重大影响。

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