Roach Michael C, Bradley Jeffrey D, Robinson Cliff G
Department of Radiation Oncology, Washington University School of Medicine, Saint Louis, MO, USA.
J Thorac Dis. 2018 Aug;10(Suppl 21):S2465-S2473. doi: 10.21037/jtd.2018.01.153.
Radiation therapy is the foundation for treatment of locally advanced non-small cell lung cancer (NSCLC), a disease that is often inoperable and has limited long term survival. Local control of disease is strongly linked to patient survival and continues to be problematic despite continued attempts at changing the dose and fractionation of radiation delivered. Technological advancements such as 4-dimensional computed tomography (CT) based planning, positron emission tomography (PET) based target delineation, and daily image guidance have allowed for ever more accurate and conformal treatments. A limit to dose escalation with conventional fractions of 2 Gy once per day appears to have been reached at 60 Gy in the randomized trial Radiation Therapy Oncology Group (RTOG) 0617. Higher doses were surprisingly associated with worse overall survival. Approaches other than conventional dose escalation have been explored to better control disease including accelerating treatment to limit tumor repopulation both with hyperfractionation and its multiple small (<2 Gy) fractions each day and with hypofractionation and its single larger (>2 Gy) fraction each day. These accelerated regimens are increasingly being used with concurrent chemotherapy, and multiple institutions have reported it as tolerable. Tailoring treatment to individual patient disease and normal anatomic characteristics has been explored with isotoxic dose escalation up to the tolerance of organs at risk, with both hyperfractionation and hypofractionation. Metabolic imaging during and after treatment is increasingly being used to boost doses to residual disease. Boost doses have included moderate hypofractionation of 2-4 Gy, and more recently extreme hypofractionation with stereotactic body radiation therapy (SBRT). In spite of all these changes in dose and fractionation, lung and cardiovascular toxicity remain obstacles that limit disease control and patient survival.
放射治疗是局部晚期非小细胞肺癌(NSCLC)治疗的基础,这种疾病通常无法手术且长期生存率有限。疾病的局部控制与患者生存密切相关,尽管不断尝试改变放射剂量和分割方式,但仍然存在问题。诸如基于四维计算机断层扫描(CT)的计划、基于正电子发射断层扫描(PET)的靶区勾画以及每日图像引导等技术进步,使得治疗更加精确和适形。在放射治疗肿瘤学组(RTOG)0617的随机试验中,每天一次给予2 Gy常规分割剂量递增似乎在60 Gy时达到了极限。令人惊讶的是,更高剂量与更差的总生存率相关。人们探索了常规剂量递增以外的其他方法来更好地控制疾病,包括加速治疗以限制肿瘤再增殖,这既可以通过超分割及其每天多个小剂量(<2 Gy)分割,也可以通过低分割及其每天单个大剂量(>2 Gy)分割来实现。这些加速方案越来越多地与同步化疗联合使用,多个机构报告其耐受性良好。已经探索了根据个体患者的疾病和正常解剖特征进行治疗,通过等毒性剂量递增至危及器官的耐受剂量,包括超分割和低分割。治疗期间和治疗后的代谢成像越来越多地用于提高对残留疾病的剂量。提高剂量包括2 - 4 Gy的中度低分割,以及最近采用立体定向体部放射治疗(SBRT)的极端低分割。尽管在剂量和分割方面有所有这些变化,但肺部和心血管毒性仍然是限制疾病控制和患者生存的障碍。