Ardizzoni A, Tiseo M
Azienda Ospedaliera-Universitaria, Parma, Italy.
J Chemother. 2004 Nov;16 Suppl 4:104-7. doi: 10.1179/joc.2004.16.Supplement-1.104.
An increasing number of patients with advanced non-small cell lung cancer (NSCLC) progressing after front-line chemotherapy are still in good performance status and willing to receive further treatment. Several drugs have been tested in this setting of treatment, but the only agent registered world-wide for second-line chemotherapy of advanced NSCLC is docetaxel. This drug, at dose of 75 mg/m2 every three weeks, has been the standard of care as second-line chemotherapy since 2000, based on two trials that reported improved survival times and quality of life when comparing with best supportive care (TAX 317) and with ifosfamide or vinorelbine (TAX 320). Docetaxel, given at this dose and schedule, resulted in significant haematological toxicity, with many patients at risk for neutropenic fever. Pemetrexed is a novel multitargeted antifolate agent with single-agent activity in first- and second-line treatment of NSCLC. In a phase III study in 571 patients pemetrexed, comparing with docetaxel in second-line chemotherapy, demonstrated clinically equivalent therapeutic outcomes, but a more favourable haematological toxicity profile, with fewer episodes of neutropenia, neutropenic fever, and infections and less use of granulocyte colony-stimulating factor support. Others several agents have been evaluated for the second-line treatment of patients with non-small cell lung cancer, but no comparative phase III studies with docetaxel has been carried out. The epidermal growth factor receptor-tyrosine kinase inhibitors gefitinib (ZD1839, Iressa) and erlotinib (OSI 774, Tarceva) have been evaluated in the second- and third-line setting. Both drugs have demonstrated interesting response rates and toxicity profile and, in particular, erlotinib evidenced a survival advantage of 2 months respect placebo in recent phase III trial. Future developments are likely to value poli-chemotherapy or combination chemotherapy with EGFR tyrosine kinase inhibitors in second-line treatment of advanced NSCLC.
越来越多一线化疗后病情进展的晚期非小细胞肺癌(NSCLC)患者仍具有良好的身体状况,并愿意接受进一步治疗。在这种治疗背景下,已有多种药物进行了试验,但全球唯一获批用于晚期NSCLC二线化疗的药物是多西他赛。自2000年以来,基于两项试验,该药物每三周75mg/m²的剂量一直作为二线化疗的标准治疗方案,这两项试验报告称,与最佳支持治疗(TAX 317)以及与异环磷酰胺或长春瑞滨(TAX 320)相比,其生存期和生活质量均有所改善。按照此剂量和给药方案使用多西他赛会导致显著的血液学毒性,许多患者有发生中性粒细胞减少性发热的风险。培美曲塞是一种新型多靶点抗叶酸药物,在NSCLC的一线和二线治疗中具有单药活性。在一项针对571例患者的III期研究中,培美曲塞与多西他赛用于二线化疗相比,显示出临床等效的治疗效果,但血液学毒性特征更优,中性粒细胞减少、中性粒细胞减少性发热和感染的发生率更低,粒细胞集落刺激因子支持的使用也更少。其他几种药物也已被评估用于非小细胞肺癌患者的二线治疗,但尚未开展与多西他赛对比的III期研究。表皮生长因子受体酪氨酸激酶抑制剂吉非替尼(ZD1839,易瑞沙)和厄洛替尼(OSI 774,特罗凯)已在二线和三线治疗中进行了评估。这两种药物均显示出令人感兴趣的缓解率和毒性特征,特别是在最近的III期试验中,厄洛替尼相对于安慰剂显示出2个月的生存优势。未来的发展可能会重视在晚期NSCLC二线治疗中采用多药化疗或联合EGFR酪氨酸激酶抑制剂进行化疗。