Tanaka Fumihiro, Yoneda Kazue
Second Department of Surgery (Chest Surgery), University of Occupational and Environmental Health, Japan, Iseigaoka 1-1, Yahata-nishi-ku, Kitakyusyu, 807-8555, Japan.
Surg Today. 2016 Jan;46(1):25-37. doi: 10.1007/s00595-015-1174-7. Epub 2015 Apr 30.
Non-small cell lung cancer (NSCLC) accounts for 80-90 % of cases of primary lung cancer. Although surgery is recommended as the primary treatment for early-stage NSCLC, the prognosis is unsatisfactory even when complete resection is achieved. Recent clinical trials have shown that postoperative adjuvant chemotherapy with cytotoxic agents, namely uracil-tegafur (UFT) for stage IA (>2 cm in diameter)-IB patients or cisplatin-based regimens for stage II-IIIA patients, improves the prognosis, and adjuvant chemotherapy is recommended as the "standard treatment of care." However, adjuvant chemotherapy provides only a modest 5-year survival benefit of 4 % and may sometimes be fatal. To improve the risk-benefit balance of adjuvant chemotherapy, targeting agents such as antibodies against vascular endothelial growth factor (VEGF) and tyrosine-kinase inhibitors of epidermal growth factor receptor (EGFR-TKIs) are being evaluated in ongoing adjuvant trials. Another promising approach may be the individualization of adjuvant chemotherapy based on biomarkers that may predict the prognosis or benefits associated with adjuvant chemotherapy. The current status and future perspectives of adjuvant chemotherapy for NSCLC are reviewed and discussed.
非小细胞肺癌(NSCLC)占原发性肺癌病例的80 - 90%。尽管手术被推荐为早期NSCLC的主要治疗方法,但即便实现了完全切除,预后仍不尽人意。近期临床试验表明,对直径>2 cm的IA期 - IB期患者采用细胞毒性药物优福定(UFT)进行术后辅助化疗,对II期 - IIIA期患者采用以顺铂为基础的化疗方案,可改善预后,辅助化疗被推荐为“标准治疗方案”。然而,辅助化疗仅能带来适度4%的5年生存获益,且有时可能是致命的。为改善辅助化疗的风险效益平衡,正在进行的辅助试验中对诸如抗血管内皮生长因子(VEGF)抗体和表皮生长因子受体酪氨酸激酶抑制剂(EGFR - TKIs)等靶向药物进行评估。另一种有前景的方法可能是基于可预测辅助化疗预后或获益的生物标志物对辅助化疗进行个体化。本文对NSCLC辅助化疗的现状及未来展望进行综述和讨论。