Universitätsklinik für Radiotherapie und Radio-Onkologie, LKH, Universitätsklinikum, Paracelsus Medizinische Privatuniversität, Müllner Hauptstr. 48, 5020, Salzburg, Austria.
Universitätsklinik für Radio-Onkologie, Inselspital, Universität Bern, Bern, Switzerland.
Strahlenther Onkol. 2021 Feb;197(2):89-96. doi: 10.1007/s00066-020-01723-8. Epub 2020 Dec 10.
Due to its low fractionation sensitivity, also known as "alpha/beta ratio," in relation to its surrounding organs at risk, prostate cancer is predestined for hypofractionated radiation schedules assuming an increased therapeutic ratio compared to normofractionated regimens. While moderate hypofractionation (2.2-4 Gy) has been proven to be non-inferior to normal fractionation in several large randomized trials for localized prostate cancer, level I evidence for ultrahypofractionation (>4 Gy) was lacking until recently. An accumulating body of non-randomized evidence has recently been strengthened by the publication of two randomized studies comparing ultrahypofractionation with a normofractionated schedule, i.e., the Scandinavian HYPO-RT trial by Widmark et al. and the first toxicity results of the PACE‑B trial. In this review, we aim to give a brief overview of the current evidence of ultrahypofractionation, make an overall assessment of the level of evidence, and provide recommendations and requirements that should be followed before introducing ultrahypofractionation into routine clinical use.
由于前列腺癌与周围危及器官相比,其分割敏感性较低,也称为“α/β 比值”,因此假设与常规分割方案相比具有更高的治疗比,前列腺癌适合进行低分割放射治疗方案。虽然中度低分割(2.2-4Gy)已在几项大型随机临床试验中被证明与局部前列腺癌的常规分割方案不劣效,但直到最近才出现超分割(>4Gy)的 I 级证据。最近,大量非随机证据得到了两项随机研究的支持,这两项研究比较了超分割与常规分割方案,即 Widmark 等人进行的斯堪的纳维亚 HYPO-RT 试验和 PACE-B 试验的首次毒性结果。在这篇综述中,我们旨在简要概述超分割的现有证据,对证据水平进行全面评估,并在将超分割引入常规临床应用之前提供应遵循的建议和要求。