Department of Investigational Cancer Therapeutics, Phase I Clinical Trials Program, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.
Clin Cancer Res. 2012 Nov 15;18(22):6356-63. doi: 10.1158/1078-0432.CCR-12-0178. Epub 2012 Sep 26.
We analyzed the outcomes of single-agent phase II clinical trials in non-small cell lung cancer (NSCLC) to determine trial parameters that predicted clinical activity.
Data on response rate (RR), progression-free survival (PFS), and overall survival (OS) from all English language, single-agent phase II trials in advanced/metastatic NSCLC indexed by PubMed (January 2000 through December 2009) were abstracted.
A total of 143 single-agent phase II trials (7,701 patients) were identified. The median RR was 10%, PFS 2.8 months, and OS 7.6 months. RR and PFS correlated with OS (r = 0.46, P < 0.001, r = 0.52, P < 0.001, respectively) and RR correlated with PFS (r = 0.61, P < 0.001). Treatment arms enriched for patients with molecular targets had a higher median RR (48.8% vs. 9.7%, P = 0.005), longer median PFS (6 vs. 2.8 months, P = 0.005), and OS (11.3 vs. 7.5 months, P = 0.05) as compared with those of unselected patients. In multivariate analysis, only studies enriched for patients with molecular targets or including drugs that eventually gained FDA/EMA approval were associated with a higher RR, and longer PFS/OS.
In phase II trials in NSCLC, RR and PFS correlated with OS. Studies enriched for patients with putative molecular drug targets were associated with higher therapeutic benefit as compared with those of unselected populations.
我们分析了非小细胞肺癌(NSCLC)单药 II 期临床试验的结果,以确定预测临床疗效的试验参数。
从 PubMed 索引的所有英文语言、晚期/转移性 NSCLC 单药 II 期临床试验(2000 年 1 月至 2009 年 12 月)中提取关于客观缓解率(RR)、无进展生存期(PFS)和总生存期(OS)的数据。
共确定了 143 项单药 II 期试验(7701 例患者)。中位 RR 为 10%,PFS 为 2.8 个月,OS 为 7.6 个月。RR 和 PFS 与 OS 相关(r = 0.46,P < 0.001,r = 0.52,P < 0.001),RR 与 PFS 相关(r = 0.61,P < 0.001)。针对分子靶点富集的治疗组具有更高的中位 RR(48.8%比 9.7%,P = 0.005)、更长的中位 PFS(6 比 2.8 个月,P = 0.005)和 OS(11.3 比 7.5 个月,P = 0.05)。多变量分析显示,仅针对分子靶点患者富集或包含最终获得 FDA/EMA 批准的药物的研究与更高的 RR 和更长的 PFS/OS 相关。
在 NSCLC 的 II 期试验中,RR 和 PFS 与 OS 相关。针对潜在分子药物靶点患者富集的研究与未选择人群相比,具有更高的治疗获益。