首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Response to 'Stereotactic ablative radiotherapy in the framework of classical radiobiology: response to Drs. Brown, Diehn, and Loo.' (Int J Radiat Oncol Biol Phys 2011;79:1599-1600) and 'Influence of tumor hypoxia on stereotactic ablative radiotherapy (SABR): response to Drs. Mayer and Timmerman.' (Int J Radiation Oncol Biol Phys 2011;78:1600).
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Response to 'Stereotactic ablative radiotherapy in the framework of classical radiobiology: response to Drs. Brown, Diehn, and Loo.' (Int J Radiat Oncol Biol Phys 2011;79:1599-1600) and 'Influence of tumor hypoxia on stereotactic ablative radiotherapy (SABR): response to Drs. Mayer and Timmerman.' (Int J Radiation Oncol Biol Phys 2011;78:1600).

机译:对“在经典放射生物学框架内的立体定向消融放疗:对Brown,Diehn和Loo博士的回应”。 (Int J Radiat Oncol Biol Phys 2011; 79:1599-1600)和“肿瘤缺氧对立体定向消融放射治疗(SABR)的影响:对Mayer和Timmerman博士的反应。” (Int J Radiation Oncol Biol Phys 2011; 78:1600)。

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To the Editor: In a recent issue of the International Journal of Radiation, Biology, and Physics, Drs. Meyer and Timmerman (1) and Brown et al. (2) discussed their differing views as to how to approach hypoxic protection in treating tumors with stereotactic body radiotherapy (SBRT) or stereotactic ablative radiotherapy (SABR). Brown et al. (3) previously suggested that hypoxic radiosensitizers will improve the response of tumors to SBRT or SABR because the currently used SBRT or, SABR protocols are unable to eradicate all the hypoxic cells in target tumors. Meyer and Timmerman (1), however, contended that fractionation of SBRT or SABR with a hypoxia transition dose per fraction would allow hypoxic cells to be reoxygenated during the fractionation intervals, thereby rendering tumor cells vulnerable to subsequent irradiations with a hypoxia transition dose. It is our view that, as Brown et al. stated (2), it would be difficult to identify precisely the hypoxic transition dose before each fractionated radiation, at least with presently available technology. In addition, we would like to point out an additional problem in the approach Meyer and Timmerman proposed. In the particular tumor model and survival curve that Meyer and Timmerman used for their discussion, as shown in their Fig. 1, the hypoxia transition dose was suggested to be 9 Gy. We believe that irradiation of tumors with 9-Gy ranges, especially when it is repeated, will cause considerable vascular damage throughout the tumors and deplete oxygen supply to tumor cells, leading to deoxygenation of oxic tumor cells rather than reoxygenation of hypoxic tumor cells. Consequently, expecting that "the hypoxic proportion remains constant (or less) between fractions," as Meyer and Timmerman stated, is quite unrealistic when tumors are irradiated with doses as high as 9 Gy per fraction.
机译:致编辑:在最近一期的《国际辐射,生物学与物理学杂志》上,Dr。 Meyer和Timmerman(1)和Brown等。 (2)讨论了他们在采用立体定向放射疗法(SBRT)或立体定向消融放射疗法(SABR)治疗肿瘤时如何采取低氧保护的不同观点。布朗等。 (3)以前认为低氧放射增敏剂将改善肿瘤对SBRT或SABR的反应,因为当前使用的SBRT或SABR方案无法根除靶肿瘤中的所有低氧细胞。然而,Meyer和Timmerman(1)认为,以分数为单位的低氧过渡剂量对SBRT或SABR进行分级分离,可使低氧细胞在分级间隔内重新充氧,从而使肿瘤细胞容易受到随后的低氧过渡剂量照射。我们认为,正如Brown等人所述。根据文献(2),至少在目前可用的技术下,很难在每次分次辐射之前准确确定低氧过渡剂量。另外,我们还要指出Meyer和Timmerman提出的方法中的另一个问题。如图1所示,在Meyer和Timmerman用于讨论的特定肿瘤模型和生存曲线中,低氧过渡剂量建议为9 Gy。我们认为9-Gy范围的肿瘤照射,特别是当其重复照射时,将在整个肿瘤中引起相当大的血管损伤,并耗尽向肿瘤细胞的氧气供应,从而导致含氧肿瘤细胞脱氧而不是低氧肿瘤细胞复氧。因此,当以每部分高达9 Gy的剂量辐照肿瘤时,如Meyer和Timmerman所言,期望“各部分之间的低氧比例保持恒定(或更低)”是不现实的。

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