Belani C P
Department of Medicine, University of Pittsburgh School of Medicine, University of Pittsburgh Cancer Institute, PA 15213, USA.
Semin Oncol. 1998 Jun;25(3 Suppl 8):10-4.
The options available to patients with advanced non-small cell lung cancer (NSCLC) resistant or refractory to first-line chemotherapy are very limited. The older-generation drugs (etoposide, vindesine, epirubicin, and cisplatin) that are active against previously untreated NSCLC do not achieve a response rate greater than 10% when used in the second-line setting. The newer-generation agents with activity in previously untreated NSCLC include carboplatin, paclitaxel, docetaxel, vinorelbine, gemcitabine, and irinotecan. Although NSCLC remains relatively resistant to chemotherapy, the fact that second-line chemotherapy is being considered is tribute to the progress being made with first-line therapy. The taxanes have clearly become the agents of the 1990s. The activity of paclitaxel in the second-line setting is not well-defined, and the response rates have ranged from 0% to 3 31% using various schedules. However, docetaxel achieved response rates of 15% to 22% in five phase II trials, with a clinically meaningful survival rate of 25% at 1 year in one of the studies. Randomized trials of docetaxel versus best supportive care and of docetaxel versus vinorelbine or ifosfamide are in progress. The efficacy of vinorelbine and irinotecan in the second-line setting have been dismal. Gemcitabine demonstrated a response rate of 25% in a recently reported trial and needs further investigation. Further progress may come from a wider investigation of novel agents and their combination with biological and other selective therapies.
对于一线化疗耐药或难治的晚期非小细胞肺癌(NSCLC)患者,可选择的治疗方案非常有限。对未经治疗的NSCLC有效的老一代药物(依托泊苷、长春地辛、表柔比星和顺铂)在二线治疗中使用时,缓解率不超过10%。在未经治疗的NSCLC中具有活性的新一代药物包括卡铂、紫杉醇、多西他赛、长春瑞滨、吉西他滨和伊立替康。尽管NSCLC对化疗仍相对耐药,但考虑二线化疗这一事实得益于一线治疗所取得的进展。紫杉烷类药物显然已成为20世纪90年代的主要药物。紫杉醇在二线治疗中的活性尚不明确,采用不同方案时缓解率在0%至33.1%之间。然而,在五项II期试验中,多西他赛的缓解率为15%至22%,其中一项研究中1年的临床意义生存率为25%。多西他赛与最佳支持治疗以及多西他赛与长春瑞滨或异环磷酰胺的随机试验正在进行中。长春瑞滨和伊立替康在二线治疗中的疗效一直不佳。吉西他滨在最近报道的一项试验中显示缓解率为25%,需要进一步研究。进一步的进展可能来自对新型药物及其与生物和其他选择性疗法联合应用的更广泛研究。