D'Addario Giannicola, Pintilie Melania, Leighl Natasha B, Feld Ronald, Cerny Thomas, Shepherd Frances A
Kantonsspital St Gallen, Departement Innere Medizin, Fachbereich Onkologie-Haematologie, Rorschacherstrasse 95, 9007 St Gallen, Switzerland.
J Clin Oncol. 2005 May 1;23(13):2926-36. doi: 10.1200/JCO.2005.03.045. Epub 2005 Feb 22.
This meta-analysis was performed to compare the activity, efficacy and toxicity of platinum-based versus non-platinum-based chemotherapy in patients with advanced non-small-cell lung cancer.
Randomized phase II and III clinical trials comparing first-line palliative platinum-based chemotherapy with the same regimen without platinum or with platinum replaced by a nonplatinum agent were identified by electronic searches of Medline, Embase, and Cancerlit, and hand searches of relevant abstract books and reference lists. Response rates, 1-year survival, and toxicity were analyzed. Subgroups of trials using third-generation agents were compared.
Thirty-seven assessable trials were identified including 7,633 patients. A 62% increase in the odds ratio (OR) for response was attributable to platinum-based therapy (OR, 1.62; 95% CI, 1.46 to 1.8; P < .0001). The 1-year survival rate was increased by 5% with platinum-based regimens (34% v 29%; OR, 1.21; 95% CI, 1.09 to 1.35; P = .0003). No statistically significant increase in 1-year survival was found when platinum therapies were compared to third-generation-based combination regimens (OR, 1.11; 95% CI, 0.96 to 1.28; P = .17). The toxicity of platinum-based regimens was significantly higher for hematologic toxicity, nephrotoxicity, and nausea and vomiting, but not for neurotoxicity, febrile neutropenia rate, or toxic death rate.
Response is significantly higher with platinum-containing regimens. One-year survival was not significantly prolonged when platinum-based therapies were compared with third-generation-based combination regimens. Toxicity is generally higher for platinum-based regimens.
进行这项荟萃分析以比较铂类与非铂类化疗在晚期非小细胞肺癌患者中的活性、疗效和毒性。
通过对Medline、Embase和Cancerlit进行电子检索,以及对相关摘要书籍和参考文献列表进行手工检索,确定了将一线姑息性铂类化疗与不含铂的相同方案或用非铂类药物替代铂的方案进行比较的随机II期和III期临床试验。分析了缓解率、1年生存率和毒性。对使用第三代药物的试验亚组进行了比较。
共确定了37项可评估试验,包括7633例患者。铂类疗法使缓解的优势比(OR)增加了62%(OR,1.62;95%CI,1.46至1.8;P<.0001)。铂类方案使1年生存率提高了5%(34%对29%;OR,1.21;95%CI,1.09至1.35;P=.0003)。当将铂类疗法与基于第三代药物的联合方案进行比较时,未发现1年生存率有统计学意义的增加(OR,1.11;95%CI,0.96至1.28;P=.17)。铂类方案的血液学毒性、肾毒性以及恶心和呕吐的毒性明显更高,但神经毒性、发热性中性粒细胞减少率或毒性死亡率并非如此。
含铂方案的缓解率明显更高。当将铂类疗法与基于第三代药物的联合方案进行比较时,1年生存率未显著延长。铂类方案的毒性通常更高。