Harper Peter
Medical Oncology, Guy's and St. Thomas Hospital, London, United Kingdom.
Semin Oncol. 2003 Aug;30(4 Suppl 10):2-12. doi: 10.1016/s0093-7754(03)00279-3.
Platinum-based chemotherapy regimens comprise a standard treatment approach for patients with advanced and metastatic non-small cell lung cancer (NSCLC). Based on results from randomized studies and meta-analyses, it has been established that such therapy significantly improves survival and maintains or improves quality of life relative to best supportive care. Combinations of cisplatin or carboplatin with gemcitabine, a newer-generation nucleoside antimetabolite with single-agent activity of 20% to 26% in advanced NSCLC, have shown antitumor activity and are well tolerated. In many studies in the advanced-disease setting, carboplatin has replaced cisplatin because of its improved nonhematologic toxicity profile and greater ease of administration. Encouraging results in the phase II setting have led to the design and implementation of several phase III studies of gemcitabine/carboplatin in the treatment of patients with advanced NSCLC. Results of three phase III trials involving more than 900 patients not previously treated with chemotherapy are discussed herein. These studies compared gemcitabine/carboplatin versus gemcitabine alone, gemcitabine/carboplatin versus gemcitabine/cisplatin, and gemcitabine/carboplatin versus mitomycin/ifosfamide/cisplatin (MIP), a regimen commonly used in Europe. Results show that gemcitabine/carboplatin efficacy was equivalent or superior to that achieved with single-agent gemcitabine or other platinum-based treatments. The regimen was well tolerated overall, and available data from one study show a significant improvement in quality of life. Thus, gemcitabine/carboplatin appears to be a viable option in the first-line treatment of advanced NSCLC. The results of one study reviewed suggest that gemcitabine/carboplatin can be considered for the treatment of patients over 70 years old.
铂类化疗方案是晚期和转移性非小细胞肺癌(NSCLC)患者的标准治疗方法。基于随机研究和荟萃分析的结果,已证实相对于最佳支持治疗,此类疗法可显著提高生存率,并维持或改善生活质量。顺铂或卡铂与吉西他滨联合使用,吉西他滨是一种新一代核苷抗代谢药物,在晚期NSCLC中的单药活性为20%至26%,已显示出抗肿瘤活性且耐受性良好。在许多晚期疾病的研究中,卡铂已取代顺铂,因为其非血液学毒性特征有所改善且给药更简便。II期研究的鼓舞人心的结果促使设计并开展了多项吉西他滨/卡铂治疗晚期NSCLC患者的III期研究。本文讨论了三项涉及900多名未接受过化疗的患者的III期试验结果。这些研究比较了吉西他滨/卡铂与单用吉西他滨、吉西他滨/卡铂与吉西他滨/顺铂,以及吉西他滨/卡铂与丝裂霉素/异环磷酰胺/顺铂(MIP,欧洲常用方案)。结果表明,吉西他滨/卡铂的疗效等同于或优于单用吉西他滨或其他铂类治疗。该方案总体耐受性良好,一项研究的现有数据显示生活质量有显著改善。因此,吉西他滨/卡铂似乎是晚期NSCLC一线治疗的可行选择。一项综述研究的结果表明,70岁以上患者的治疗可考虑使用吉西他滨/卡铂。