Rigas James R
Norris Cotton Cancer Center, Dartmouth Medical School, Lebanon, New Hampshire 03756, USA.
Oncologist. 2004;9 Suppl 2:16-23. doi: 10.1634/theoncologist.9-suppl_2-16.
Platinum-based chemotherapy is the treatment of choice for patients with non-small cell lung cancer (NSCLC). As a result of their single-agent activities and synergistic effects, taxane-platinum combinations are often used as first-line therapy for this disease. Four large, multicenter, randomized phase III clinical trials (the TAX 326 trial, the Southwest Oncology Group 9509 trial, the Italian Lung Cancer Project, and the Eastern Cooperative Oncology Group 1594 trial) have compared taxane-platinum combinations (docetaxel and paclitaxel) with other platinum combinations (vinorelbine and gemcitabine) in chemotherapy-naïve patients with good performance status scores and advanced disease. The end points for these large randomized clinical trials were survival, response rate, adverse events, and quality of life (QOL). Of the taxane-platinum combinations tested, docetaxel-cisplatin was the only platinum combination to yield survival and response rates superior to another platinum combination. In adverse event terms, the taxane-platinum combination of paclitaxel-carboplatin demonstrated less grade 3 or 4 neutropenia and lower rates of febrile neutropenia than other taxane-platinum combinations but higher rates of irreversible grade 3 or 4 peripheral neuropathy than any of the other taxane-platinum combinations. Additional differences emerged when QOL data were evaluated. The docetaxel-platinum combination demonstrated broad QOL benefits for patients receiving this combination, and this benefit was not observed with the other platinum or taxane-platinum combinations. As our use of these taxane-platinum combinations expands, these differences in survival, response rate, adverse events, and QOL will permit us to better balance our treatment goals for all patients with all stages of NSCLC.
铂类化疗是非小细胞肺癌(NSCLC)患者的首选治疗方法。由于紫杉烷类药物的单药活性及其协同作用,紫杉烷 - 铂联合方案常被用作该病的一线治疗。四项大型、多中心、随机III期临床试验(TAX 326试验、西南肿瘤协作组9509试验、意大利肺癌项目以及东部肿瘤协作组1594试验)在体能状态评分良好且患有晚期疾病的初治患者中,比较了紫杉烷 - 铂联合方案(多西他赛和紫杉醇)与其他铂类联合方案(长春瑞滨和吉西他滨)。这些大型随机临床试验的终点指标包括生存率、缓解率、不良事件和生活质量(QOL)。在所测试的紫杉烷 - 铂联合方案中,多西他赛 - 顺铂是唯一一种生存率和缓解率优于另一种铂类联合方案的铂类联合方案。在不良事件方面,紫杉醇 - 卡铂的紫杉烷 - 铂联合方案与其他紫杉烷 - 铂联合方案相比,3级或4级中性粒细胞减少症更少,发热性中性粒细胞减少症发生率更低,但3级或4级不可逆外周神经病变发生率高于其他任何紫杉烷 - 铂联合方案。在评估生活质量数据时出现了其他差异。多西他赛 - 铂联合方案对接受该联合方案的患者显示出广泛的生活质量益处,而其他铂类或紫杉烷 - 铂联合方案未观察到这种益处。随着我们对这些紫杉烷 - 铂联合方案的应用不断扩大,这些在生存率、缓解率、不良事件和生活质量方面的差异将使我们能够更好地平衡所有NSCLC各阶段患者的治疗目标。