Cosset J-M
GIE Charlebourg, groupe Amethyst, 65, avenue Foch, 92250 La Garenne-Colombes, France.
Cancer Radiother. 2017 Oct;21(6-7):447-453. doi: 10.1016/j.canrad.2017.06.006. Epub 2017 Aug 26.
For prostate cancer, hypofractionation has been based since 1999 on radiobiological data, which calculated a very low alpha/beta ratio (1.2 to 1.5Gy). This suggested that a better local control could be obtained, without any toxicity increase. Consequently, two types of hypofractionated schemes were proposed: "moderate" hypofractionation, with fractions of 2.5 to 4Gy, and "extreme" hypofractionation, utilizing stereotactic techniques, with fractions of 7 to 10Gy. For moderate hypofractionation, the linear-quadratic (LQ) model has been used to calculate the equivalent doses of the new protocols. The available trials have often shown a "non-inferiority", but no advantage, while the equivalent doses calculated for the hypofractionated arms were sometimes very superior to the doses of the conventional arms. This finding could suggest either an alpha/beta ratio lower than previously calculated, or a negative impact of other radiobiological parameters, which had not been taken into account. For "extreme" hypofractionation, the use of the LQ model is discussed for high dose fractions. Moreover, a number of radiobiological questions are still pending. The reduced overall irradiation time could be either a positive point (better local control) or a negative one (reduced reoxygenation). The prolonged duration of the fractions could lead to a decrease of efficacy (because allowing for reparation of sublethal lesions). Finally, the impact of the large fractions on the microenvironment and/or immunity remains discussed. The reported series appear to show encouraging short to mid-term results, but the results of randomized trials are still awaited. Today, it seems reasonable to only propose those extreme hypofractionated schemes to well-selected patients, treating small volumes with high-level stereotactic techniques.
对于前列腺癌,自1999年起,大分割放疗就基于放射生物学数据,该数据计算出极低的α/β比值(1.2至1.5戈瑞)。这表明在不增加任何毒性的情况下,可以获得更好的局部控制。因此,提出了两种大分割放疗方案:“适度”大分割放疗,每次分割剂量为2.5至4戈瑞;“极端”大分割放疗,采用立体定向技术,每次分割剂量为7至10戈瑞。对于适度大分割放疗,线性二次(LQ)模型已被用于计算新方案的等效剂量。现有试验常常显示出“非劣效性”,但没有优势,而大分割放疗组计算出的等效剂量有时远高于传统放疗组的剂量。这一发现可能意味着α/β比值低于先前计算的值,或者是其他未被考虑的放射生物学参数产生了负面影响。对于“极端”大分割放疗,高剂量分割时LQ模型的使用存在争议。此外,一些放射生物学问题仍未解决。总照射时间缩短可能是一个积极因素(更好的局部控制),也可能是消极因素(再氧合减少)。分割时间延长可能导致疗效降低(因为允许亚致死性损伤修复)。最后,大分割剂量对微环境和/或免疫的影响仍在讨论中。已报道的系列研究似乎显示出令人鼓舞的短期至中期结果,但仍在等待随机试验的结果。如今,似乎只有将那些极端大分割放疗方案推荐给精心挑选的患者才合理,即使用高水平立体定向技术治疗小体积肿瘤。