Global Access, F. Hoffmann-La Roche, Basel, Switzerland.
Cytel, Waltham, Massachusetts.
JAMA Netw Open. 2021 Nov 1;4(11):e2134299. doi: 10.1001/jamanetworkopen.2021.34299.
Evidence regarding real-world effectiveness of therapies for patients with advanced non-small cell lung cancer (NSCLC) whose tumors are resistant to platinum-based chemotherapy is lacking.
To compare the effectiveness of the immune checkpoint inhibitors atezolizumab (programmed cell death ligand 1 inhibitor) and nivolumab (programmed cell death 1 inhibitor) and the chemotherapy drug docetaxel in patients with advanced NSCLC resistant to platinum-based chemotherapy.
DESIGN, SETTING, AND PARTICIPANTS: This comparative effectiveness study compared patients aged 18 years or older with advanced NSCLC who initiated atezolizumab, docetaxel, or nivolumab and who had previously been exposed to platinum-based chemotherapy using nationally representative real-world data from more than 280 US cancer clinics. Patients were followed-up from May 2011 to March 2020. Data analysis was performed between April and June 2021. Comparisons of interest were between atezolizumab vs docetaxel and atezolizumab vs nivolumab.
Initiation of atezolizumab, nivolumab, or docetaxel monotherapy.
The main outcome was overall survival (OS).
A total of 3336 patients (mean [SD] age, 67.1 [9.49] years; 1820 [54.6%] men and 1516 [45.4%] women) were assessed in the main analysis, including 206 patients receiving atezolizumab, 500 receiving docetaxel, and 2630 receiving nivolumab. Patients receiving atezolizumab were older than those treated with docetaxel (mean age [SD], 68.3 [9.4] years vs 65.6 [9.5] years), and were more likely to have been treated in an academic setting (39 patients [18.9%]) than those receiving docetaxel (49 patients [9.8%]) and nivolumab (128 patients [4.9%]). After adjustment for baseline characteristics, atezolizumab was associated with a significantly longer OS compared with docetaxel (adjusted hazard ratio [aHR], 0.79; 95% CI, 0.64-0.97). No significant difference in OS was observed between atezolizumab and nivolumab (aHR, 1.07; 95% CI, 0.89-1.28). These findings were consistent across all patient subgroups tested, and robust to plausible deviations from random missingness for Eastern Cooperative Oncology Group performance status in real-world data (eg, the tipping point for loss of a significantly beneficial effect for atezolizumab vs docetaxel was achieved if patients in the docetaxel group missing baseline Eastern Cooperative Oncology Group performance status had a mean performance status of 1.43 higher than expected).
In this comparative effectiveness study, atezolizumab was superior to docetaxel and matched nivolumab in prolonging OS in a real-world cohort of patients with advanced NSCLC who previously received platinum-based chemotherapy.
缺乏关于铂类化疗耐药的晚期非小细胞肺癌(NSCLC)患者的治疗的真实世界疗效的证据。
比较免疫检查点抑制剂阿替利珠单抗(程序性死亡配体 1 抑制剂)和纳武利尤单抗(程序性死亡 1 抑制剂)与化疗药物多西他赛在铂类化疗耐药的晚期 NSCLC 患者中的疗效。
设计、地点和参与者:这项比较有效性研究比较了 280 多家美国癌症诊所的全国代表性真实世界数据中接受阿替利珠单抗、多西他赛或纳武利尤单抗单药治疗且先前接受过铂类化疗的年龄在 18 岁或以上的晚期 NSCLC 患者。患者从 2011 年 5 月至 2020 年 3 月进行随访。数据分析于 2021 年 4 月至 6 月进行。感兴趣的比较是阿替利珠单抗与多西他赛和阿替利珠单抗与纳武利尤单抗之间的比较。
接受阿替利珠单抗、纳武利尤单抗或多西他赛单药治疗。
主要结局是总生存期(OS)。
在主要分析中,共评估了 3336 名患者(平均[SD]年龄,67.1[9.49]岁;1820[54.6%]名男性和 1516[45.4%]名女性),包括 206 名接受阿替利珠单抗治疗的患者、500 名接受多西他赛治疗的患者和 2630 名接受纳武利尤单抗治疗的患者。接受阿替利珠单抗治疗的患者比接受多西他赛治疗的患者年龄更大(平均年龄[SD],68.3[9.4]岁 vs 65.6[9.5]岁),并且更有可能在学术环境中接受治疗(39 名[18.9%])比接受多西他赛(49 名[9.8%])和纳武利尤单抗(128 名[4.9%])。在调整了基线特征后,与多西他赛相比,阿替利珠单抗的 OS 显著延长(调整后的危险比[aHR],0.79;95%CI,0.64-0.97)。与纳武利尤单抗相比,阿替利珠单抗在 OS 方面没有显著差异(aHR,1.07;95%CI,0.89-1.28)。在所有测试的患者亚组中均观察到了这些发现,并且在真实世界数据中(例如,如果多西他赛组中缺失基线东部合作肿瘤学组表现状态的患者的平均表现状态比预期高 1.43,则达到了阿替利珠单抗与多西他赛相比失去显著有益效果的转折点),从随机缺失东部合作肿瘤学组表现状态的合理偏差来看,这些发现也是稳健的。
在这项比较有效性研究中,与多西他赛相比,阿替利珠单抗在铂类化疗耐药的晚期 NSCLC 患者的真实世界队列中延长了 OS,这些患者先前接受过铂类化疗。