Gridelli Cesare, Hainsworth John
Division of Medical Oncology, SG Moscati Hospital, Via Circumvallazione, Avellino 83100, Italy.
Lung Cancer. 2002 Dec;38 Suppl 4:37-41. doi: 10.1016/s0169-5002(02)00170-8.
Increasing interest in designing chemotherapy suitable for use in the elderly and in poor performance status (PS) patients has led to clinical trials in advanced non-small cell lung cancer (NSCLC) which have demonstrated a number of important points. First, the randomized Elderly Lung Cancer Vinorelbine Study Group (ELVIS) trial makes clear that elderly patients treated with vinorelbine plus best supportive care (BSC) have significantly improved survival and quality of life when compared with patients treated with BSC alone. Secondly, the Multicenter Italian Lung Cancer in the Elderly Study (MILES) trial demonstrates that the combination of gemcitabine plus vinorelbine in this patient population does not further improve survival or quality of life as compared to single chemotherapy with vinorelbine or gemcitabine. Weekly docetaxel has considerable potential among patients judged likely to tolerate poorly cisplatin-based chemotherapy. In a trial among 39 previously untreated elderly, poor PS or medically compromised patients, weekly 36 mg/m(2) docetaxel produced a 19% response rate and 28% 1-year survival. These data compare favorably with results achieved with other single agents. Weekly, docetaxel is better tolerated than the q 3-week schedule, and myelosuppression is not severe. Weekly docetaxel is also active as second-line therapy. The combination of gemcitabine and docetaxel, both administered weekly, is well tolerated by elderly and/or poor PS patients, is active (median survival 7 months, 1-year survival 29%) and merits further study.
对设计适用于老年人及身体状况较差(PS)患者的化疗方案的兴趣日益浓厚,这促使了针对晚期非小细胞肺癌(NSCLC)的临床试验展开,这些试验揭示了一些要点。首先,老年肺癌长春瑞滨研究组(ELVIS)的随机试验明确表明,与仅接受最佳支持治疗(BSC)的患者相比,接受长春瑞滨加BSC治疗的老年患者的生存率和生活质量有显著提高。其次,意大利老年肺癌多中心研究(MILES)试验表明,在该患者群体中,吉西他滨加长春瑞滨联合用药与长春瑞滨或吉西他滨单药化疗相比,并未进一步提高生存率或生活质量。对于判定可能难以耐受基于顺铂化疗的患者,每周使用多西他赛具有相当大的潜力。在一项针对39例既往未接受治疗的老年、PS较差或存在医学问题的患者的试验中,每周使用36mg/m²多西他赛产生了19%的缓解率和28%的1年生存率。这些数据与其他单药治疗的结果相比更具优势。每周使用多西他赛的耐受性优于每3周一次的给药方案,且骨髓抑制并不严重。每周使用多西他赛作为二线治疗也有活性。吉西他滨和多西他赛均每周给药的联合方案,老年和/或PS较差的患者耐受性良好,具有活性(中位生存期7个月,1年生存率29%),值得进一步研究。