Karmanos Cancer Institute, Detroit, Michigan.
Complejo Hospitalario Universitario Insular Materno-Infantil de Gran Canaria, Universidad de Las Palmas de Gran Canaria, Las Palmas de Gran Canaria, Spain.
J Thorac Oncol. 2024 Aug;19(8):1228-1241. doi: 10.1016/j.jtho.2024.04.011. Epub 2024 Apr 18.
We report long-term outcomes from a pooled analysis of patients with previously untreated metastatic NSCLC with programmed cell death ligand 1 (PD-L1) tumor proportion score (TPS) less than 1% enrolled in phase III studies of pembrolizumab plus chemotherapy versus placebo plus chemotherapy.
This exploratory pooled analysis included individual patient data from the KEYNOTE-189 global (NCT02578680) and Japan extension (NCT03950674) studies of metastatic nonsquamous NSCLC without EGFR or ALK alterations and the KEYNOTE-407 global (NCT02775435) and People's Republic of China extension (NCT03875092) studies of metastatic squamous NSCLC. Patients received pembrolizumab or placebo plus pemetrexed and cisplatin or carboplatin in KEYNOTE-189 and pembrolizumab or placebo plus carboplatin and paclitaxel or nab-paclitaxel in KEYNOTE-407. PD-L1 TPS was centrally assessed using PD-L1 IHC 22C3 pharmDx (Agilent Technologies, Carpinteria, CA).
Overall, 442 patients were included in this analysis (pembrolizumab plus chemotherapy, n = 255; chemotherapy, n = 187). The median follow-up was 60.7 (range, 49.9‒72.0) months. Pembrolizumab plus chemotherapy improved overall survival (hazard ratio, 0.64; 95% confidence interval [CI]: 0.51‒0.79) and progression-free survival (hazard ratio, 0.66; 95% CI: 0.54‒0.81) versus chemotherapy. The 5-year overall survival rates (95% CI) were 12.5% (8.6%‒17.3%) versus 9.3% (5.6%‒14.1%). Grades 3 to 5 treatment-related adverse events occurred in 59.1% of patients for pembrolizumab plus chemotherapy and 61.3% for chemotherapy.
With approximately 5 years of follow-up, pembrolizumab plus chemotherapy provided clinically meaningful and durable improvements in survival outcomes versus chemotherapy alone in patients with previously untreated metastatic NSCLC with PD-L1 TPS less than 1%. These results continue to support pembrolizumab plus chemotherapy as a standard of care in this patient population.
gov, NCT02578680 (KEYNOTE-189 global), NCT03950674 (KEYNOTE-189 Japan extension), NCT02775435 (KEYNOTE-407 global), NCT03875092 (KEYNOTE-407 People's Republic of China extension).
我们报告了一项来自三期研究的汇总分析结果,这些研究纳入了先前未经治疗的转移性非小细胞肺癌(NSCLC)患者,这些患者的程序性死亡配体 1(PD-L1)肿瘤比例评分(TPS)<1%,且接受了帕博利珠单抗联合化疗与安慰剂联合化疗的治疗。
这项探索性的汇总分析纳入了 KEYNOTE-189 全球(NCT02578680)和日本扩展(NCT03950674)研究中无表皮生长因子受体(EGFR)或间变性淋巴瘤激酶(ALK)改变的转移性非鳞状 NSCLC 患者,以及 KEYNOTE-407 全球(NCT02775435)和中华人民共和国扩展(NCT03875092)研究中转移性鳞状 NSCLC 患者的个体患者数据。患者在 KEYNOTE-189 中接受了帕博利珠单抗或安慰剂联合培美曲塞和顺铂或卡铂治疗,在 KEYNOTE-407 中接受了帕博利珠单抗或安慰剂联合卡铂和紫杉醇或nab-紫杉醇治疗。PD-L1 TPS 采用 PD-L1 IHC 22C3 pharmDx(Agilent Technologies,加利福尼亚州卡皮廷诺拉)进行中心评估。
总体而言,这项分析纳入了 442 名患者(帕博利珠单抗联合化疗组,n=255;化疗组,n=187)。中位随访时间为 60.7 个月(范围:49.9‒72.0)。与化疗相比,帕博利珠单抗联合化疗改善了总生存期(风险比,0.64;95%置信区间[CI]:0.51‒0.79)和无进展生存期(风险比,0.66;95% CI:0.54‒0.81)。5 年总生存率(95% CI)分别为 12.5%(8.6%‒17.3%)和 9.3%(5.6%‒14.1%)。帕博利珠单抗联合化疗组和化疗组分别有 59.1%和 61.3%的患者发生 3 级或 5 级治疗相关不良事件。
在大约 5 年的随访后,与单独化疗相比,帕博利珠单抗联合化疗为 PD-L1 TPS<1%的先前未经治疗的转移性 NSCLC 患者提供了具有临床意义且持久的生存获益。这些结果继续支持帕博利珠单抗联合化疗作为该患者人群的标准治疗方案。
gov,NCT02578680(KEYNOTE-189 全球),NCT03950674(KEYNOTE-189 日本扩展),NCT02775435(KEYNOTE-407 全球),NCT03875092(KEYNOTE-407 中华人民共和国扩展)。