Alcibar Olwen Leaman, Nadal Ernest, Romero Palomar Inmaculada, Navarro-Martin Arturo
Department of Radiation Oncology, Gregorio Marañón General University Hospital, Madrid, Spain.
Department of Medical Oncology, Catalan Institute of Oncology, L'Hospitalet, Barcelona, Spain.
Transl Lung Cancer Res. 2021 Jan;10(1):529-538. doi: 10.21037/tlcr-2020-nsclc-04.
Despite adequate treatment, 50% of stage III locally advanced inoperable non-small cell lung cancer (NSCLC) patients have a locoregional relapse. Local control on early stages on the contrary, is as high as 85-90% with stereotactic body radiotherapy (SBRT). The addition of SBRT to conventional chemoradiation or its use in monotherapy in stage III NSCLC is a novel strategy to decrease local failure that has been explored by various authors. This is a systematic review of studies using SBRT in inoperable stage III NSCLC. Search results obtained 141 articles of which only 6 original studies were pointed as relevant. Three of these studies were prospective, of which 2 were phase I dose-scalation studies and remaining 3 were retrospective. In summary, SBRT outcomes on 134 patients were included. Median dose in the SBRT treatment was 22.5 Gy in 2 to 7 fractions. Obtained global toxicity was 3.7% grade 5 and 14.17% grade 3. Dose-escalation studies proposed a 2 fraction SBRT schedule of 20-24 Gy, obtaining a 78% local control rate at 1 year and an OS of 67%. Initial improvement in local control with this innovative therapeutic strategy has led to ongoing phase II and III clinical trials that will evaluate the efficiency of SBRT in stage III NSCLC clinical scenario.
尽管进行了充分治疗,但Ⅲ期局部晚期不可切除的非小细胞肺癌(NSCLC)患者中仍有50%会出现局部区域复发。相反,早期阶段采用立体定向体部放疗(SBRT)时,局部控制率高达85% - 90%。在Ⅲ期NSCLC中,将SBRT添加到传统放化疗中或用于单药治疗是一种降低局部失败的新策略,已有多位作者对此进行了探索。这是一项关于在不可切除的Ⅲ期NSCLC中使用SBRT的研究的系统评价。检索结果获得了141篇文章,其中只有6篇原始研究被认为是相关的。这些研究中有3项是前瞻性的,其中2项是Ⅰ期剂量递增研究,其余3项是回顾性的。总之,纳入了134例患者的SBRT治疗结果。SBRT治疗的中位剂量为22.5 Gy,分2至7次给予。总体毒性为5级3.7%,3级14.17%。剂量递增研究提出了20 - 24 Gy的2分次SBRT方案,1年局部控制率为78%,总生存期为67%。这种创新治疗策略在局部控制方面的初步改善已引发了正在进行的Ⅱ期和Ⅲ期临床试验,这些试验将评估SBRT在Ⅲ期NSCLC临床情况下的疗效。