Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
J Clin Oncol. 2011 Oct 1;29(28):3825-31. doi: 10.1200/JCO.2010.34.2774. Epub 2011 Sep 6.
An American Society of Clinical Oncology (ASCO) focused update updates a single recommendation (or subset of recommendations) in advance of a regularly scheduled guideline update. This document updates one recommendation of the ASCO Guideline Update on Chemotherapy for Stage IV Non-Small-Cell Lung Cancer (NSCLC) regarding switch maintenance chemotherapy.
Recent results from phase III clinical trials have demonstrated that in patients with stage IV NSCLC who have received four cycles of first-line chemotherapy and whose disease has not progressed, an immediate switch to alternative, single-agent chemotherapy can extend progression-free survival and, in some cases, overall survival. Because of limitations in the data, delayed treatment with a second-line agent after disease progression is also acceptable.
Seven randomized controlled trials of carboxyaminoimidazole, docetaxel, erlotinib, gefitinib, gemcitabine, and pemetrexed have evaluated outcomes in patients who received an immediate, non-cross resistant alternative therapy (switch maintenance) after first-line therapy.
In patients with stage IV NSCLC, first-line cytotoxic chemotherapy should be stopped at disease progression or after four cycles in patients whose disease is stable but not responding to treatment. Two-drug cytotoxic combinations should be administered for no more than six cycles. For those with stable disease or response after four cycles, immediate treatment with an alternative, single-agent chemotherapy such as pemetrexed in patients with nonsquamous histology, docetaxel in unselected patients, or erlotinib in unselected patients may be considered. Limitations of this data are such that a break from cytotoxic chemotherapy after a fixed course is also acceptable, with initiation of second-line chemotherapy at disease progression.
美国临床肿瘤学会(ASCO)的重点更新在定期指南更新之前更新单个建议(或建议子集)。本文更新了 ASCO 关于 IV 期非小细胞肺癌(NSCLC)化疗指南更新的一个建议,涉及转换维持化疗。
最近 III 期临床试验的结果表明,在接受了四周期一线化疗且疾病未进展的 IV 期 NSCLC 患者中,立即转换为替代的单一药物化疗可以延长无进展生存期,在某些情况下还可以延长总生存期。由于数据的局限性,在疾病进展后延迟使用二线药物也是可以接受的。
卡培他滨、多西他赛、厄洛替尼、吉非替尼、吉西他滨和培美曲塞七种随机对照试验评估了一线治疗后立即接受非交叉耐药替代治疗(转换维持)的患者的结局。
在 IV 期 NSCLC 患者中,在疾病进展或在疾病稳定但对治疗无反应的患者中完成四周期后应停止一线细胞毒性化疗。两药细胞毒性联合治疗不应超过六个周期。对于那些在四个周期后有稳定疾病或反应的患者,可考虑立即使用替代的单一药物化疗,如非鳞状组织学患者的培美曲塞、未选择患者的多西他赛或未选择患者的厄洛替尼。但应注意这些数据存在局限性,在完成固定疗程的细胞毒性化疗后也可以中断,在疾病进展时开始二线化疗。