Brosseau S, Naltet C, Nguenang M, Gounant V, Mordant P, Milleron B, Castier Y, Zalcman G
Service d'oncologie thoracique, CIC 1425/CLIP(2) Paris-Nord, hôpital Bichat-Claude-Bernard, Assistance publique-Hôpitaux de Paris, université Paris-Diderot, 46, rue Henri-Huchard, 75018 Paris, France.
Service de chirurgie vasculaire, thoracique et transplantation, hôpital Bichat-Claude-Bernard, Assistance publique-Hôpitaux de Paris, université Paris-Diderot, 46, rue Henri-Huchard, 75018 Paris, France.
Rev Mal Respir. 2017 Jun;34(6):618-634. doi: 10.1016/j.rmr.2016.12.001. Epub 2017 Jul 12.
Surgery is still the main treatment in early-stage of non-small cell lung cancer with 5-year survival of stage IA patients exceeding 80%, but 5-year survival of stage II patients rapidly decreasing with tumor size, N status, and visceral pleura invasion. The major metastatic risk in such patients has supported clinical research assessing systemic or loco-regional perioperative treatments. Modern phase 3 trials clearly validated adjuvant or neo-adjuvant platinum-based chemotherapy in resected stage I-III patients as a standard treatment of which value has been reassessed several independent meta-analyses, showing a 5% benefit in 5y-survival, and a decrease of the relative risk for death around from 12 to 25%. Conversely perioperative treatments were not validated for stage IA and IB patients. In more advanced stage patients, neo-adjuvant radio-chemotherapy has not been validated either. Adjuvant radiotherapy for N2 patients is currently tested in the large international phase 3 trial Lung-ART/IFCT-0503. The development of video-assisted thoracic surgery (VATS) has helped adjuvant chemotherapies for elderly patients. Perioperative targeted treatments in NSCLC with EGFR or ALK molecular alterations is currently assessed in the U.S. ALCHEMIST prospective trial. Finally, the role of immune check-points inhibitors is currently evaluated in a large international phase 3 trial testing adjuvant anti-PD-L1 monoclonal antibody, the BR31/IFCT-1401 trial, while a proof-of principle neo-adjuvant trial IONESCO/IFCT-1601, has just begun by the end of the 2016 year, with survival results of both trials expected in 5 to 7 years.
手术仍然是非小细胞肺癌早期的主要治疗方法,IA期患者的5年生存率超过80%,但II期患者的5年生存率随着肿瘤大小、N分期和脏层胸膜侵犯而迅速下降。这类患者的主要转移风险推动了评估全身或局部围手术期治疗的临床研究。现代3期试验明确证实,对于I-III期切除患者,辅助或新辅助铂类化疗是标准治疗方法,其价值已在多项独立的荟萃分析中得到重新评估,显示5年生存率提高5%,死亡相对风险降低约12%至25%。相反,围手术期治疗未在IA期和IB期患者中得到验证。在更晚期患者中,新辅助放化疗也未得到验证。N2患者的辅助放疗目前正在大型国际3期试验Lung-ART/IFCT-0503中进行测试。电视辅助胸腔镜手术(VATS)的发展有助于老年患者的辅助化疗。美国ALCHEMIST前瞻性试验目前正在评估非小细胞肺癌中具有EGFR或ALK分子改变的围手术期靶向治疗。最后,免疫检查点抑制剂的作用目前正在一项大型国际3期试验中进行评估,该试验测试辅助抗PD-L1单克隆抗体,即BR31/IFCT-1401试验,而一项原理验证性新辅助试验IONESCO/IFCT-1601于2016年底刚刚开始,两项试验的生存结果预计在5至7年内得出。