Katayama Sonja, Haefner Matthias F, Mohr Angela, Schubert Kai, Oetzel Dieter, Debus Juergen, Sterzing Florian
Department of Radiation Oncology, University Hospital Heidelberg, Germany.
J Appl Clin Med Phys. 2015 Mar 8;16(2):4964. doi: 10.1120/jacmp.v16i2.4964.
TomoEDGE is an advanced delivery form of tomotherapy which uses a dynamic secondary collimator. This plan comparison study describes the new features, their clinical applicability, and their effect on plan quality and treatment speed. For the first 45 patients worldwide that were scheduled for a treatment with TomoEdge, at least two plans were created: one with the previous "standard"mode with static jaws and 2.5 cm field width (Reg 2.5) and one with TomoEdge technique and 5 cm field width (Edge 5). If, after analysis in terms of beam on time, integral dose, dose conformity, and organ at risk sparing the treating physician decided that the Edge 5 plan was not suitable for clinical treatment, a plan with TomoEdge and 2.5 cm field width was created (Edge 2.5) and used for the treatment. Among the 45 cases, 30 were suitable for Edge 5 treatment, including treatments of the head and neck, rectal cancer, anal cancer, malignancies of the chest, breast cancer, and palliative treatments. In these cases, the use of a 5 cm field width reduced beam on time by more than 30% without compromising plan quality. The 5 cm beam could not be clinically applied to treatments of the pelvic lymph nodes for prostate cancer and to head and neck irradiations with extensive involvement of the skull, as dose to critical organs at risk such as bladder (average dose 28 Gy vs. 29 Gy, Reg 2.5 vs. Edge 5), small bowel (29% vs. 31%, Reg 2.5 vs. Edge 5) and brain (average dose partial brain 19 Gy vs. 21 Gy, Reg 2.5 vs. Edge 5) increased to a clinically relevant, yet not statistically significant, amount. TomoEdge is an advantageous extension of the tomotherapy technique that can speed up treatments and thus increase patient comfort and safety in the majority of clinical settings.
TomoEDGE是螺旋断层放疗的一种先进的放疗形式,它采用了动态二级准直器。本计划对比研究描述了其新特性、临床适用性以及对计划质量和治疗速度的影响。对于全球范围内计划接受TomoEDGE治疗的前45例患者,至少制定了两个计划:一个采用先前的“标准”模式,即静态准直器和2.5厘米射野宽度(Reg 2.5),另一个采用TomoEDGE技术和5厘米射野宽度(Edge 5)。如果在对治疗时间、积分剂量、剂量适形度和危及器官保护进行分析后,治疗医师认为Edge 5计划不适合临床治疗,则制定一个射野宽度为2.5厘米的TomoEDGE计划(Edge 2.5)并用于治疗。在这45例病例中,30例适合采用Edge 5治疗,包括头颈部、直肠癌、肛管癌、胸部恶性肿瘤、乳腺癌的治疗以及姑息治疗。在这些病例中,使用5厘米射野宽度可使治疗时间减少30%以上,且不影响计划质量。5厘米射野宽度在临床上不适用于前列腺癌盆腔淋巴结的治疗以及颅骨广泛受累的头颈部照射,因为膀胱(平均剂量28 Gy对29 Gy,Reg 2.5对Edge 5)、小肠(29%对31%,Reg 2.5对Edge 5)和脑(部分脑平均剂量19 Gy对21 Gy,Reg 2.5对Edge 5)等危及关键器官的剂量增加到了具有临床意义但无统计学显著性差异的水平。TomoEDGE是螺旋断层放疗技术的一个有利扩展,可加快治疗速度,从而在大多数临床情况下提高患者的舒适度和安全性。