Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York City, New York, USA.
Center for Thoracic Oncology, Tisch Cancer Institute and Icahn School of Medicine at Mount Sinai, New York City, New York, USA.
Cancer Med. 2022 Nov;11(22):4265-4272. doi: 10.1002/cam4.4785. Epub 2022 May 2.
Immune checkpoint inhibitors targeting the programmed cell death protein-1 (PD-1) and programmed death ligand-1 (PD-L1) axis (collectively referred to as PD[L]1i) have demonstrated clinical benefits in non-small cell lung cancer (NSCLC) patients. The purpose of this United States-based real-world study is to examine changes in the landscape of first-line therapies for NSCLC since the introduction of PD(L)1i.
Patients with NSCLC initiating first-line treatment between May 1, 2017, and October 31, 2020, were identified in the IBM MarketScan® database. Patients were assigned groups based on first-line therapy: PD(L)1i monotherapy, chemotherapy alone, PD(L)1i with chemotherapy, or targeted therapy for patients with actionable driver mutations.
A total of 5431 patients with NSCLC starting first-line treatment were identified: chemotherapy alone 2568 (47%), PD(L)1i with chemotherapy 1364 (25%), PD(L)1i monotherapy 790 (15%), and targeted therapy 709 (13%). The use of PD(L)1i monotherapy and targeted therapy remained consistent, while the percentage of patients receiving PD(L)1i with chemotherapy more than doubled. Over a third of patients in 2019 and 2020 received chemotherapy alone. Patients aged ≥65 years (odds ratio [OR]: 0.80; 95% confidence interval [CI]: 0.68-0.95), females (OR: 0.86; 95% CI: 0.74-0.98), and those with respiratory (OR: 0.82; 95% CI: 0.71-0.94) or kidney (OR: 0.56; 95% CI: 0.40-0.77) disease were less likely to have received PD(L)1i with chemotherapy than patients that received chemotherapy alone.
Since the approval of PD(L)1i for NSCLC, their use has significantly increased for first-line treatment, especially when used in combination with chemotherapy. A significant proportion of patients received chemotherapy alone.
针对程序性细胞死亡蛋白-1(PD-1)和程序性死亡配体-1(PD-L1)轴的免疫检查点抑制剂(统称为 PD[L]1i)已在非小细胞肺癌(NSCLC)患者中显示出临床获益。这项基于美国的真实世界研究旨在研究自 PD(L)1i 问世以来 NSCLC 一线治疗方案的变化。
在 IBM MarketScan®数据库中确定 2017 年 5 月 1 日至 2020 年 10 月 31 日期间开始一线治疗的 NSCLC 患者。根据一线治疗方案将患者分为以下几组:PD(L)1i 单药治疗、单纯化疗、PD(L)1i 联合化疗以及有明确驱动基因突变的靶向治疗。
共确定了 5431 名开始一线治疗的 NSCLC 患者:单纯化疗 2568 例(47%)、PD(L)1i 联合化疗 1364 例(25%)、PD(L)1i 单药治疗 790 例(15%)和靶向治疗 709 例(13%)。PD(L)1i 单药治疗和靶向治疗的使用保持稳定,而接受 PD(L)1i 联合化疗的患者比例增加了一倍以上。2019 年和 2020 年超过三分之一的患者接受单纯化疗。年龄≥65 岁的患者(比值比 [OR]:0.80;95%置信区间 [CI]:0.68-0.95)、女性(OR:0.86;95% CI:0.74-0.98)以及患有呼吸系统(OR:0.82;95% CI:0.71-0.94)或肾脏疾病(OR:0.56;95% CI:0.40-0.77)的患者接受 PD(L)1i 联合化疗的可能性低于接受单纯化疗的患者。
自 PD(L)1i 获批用于 NSCLC 以来,其在一线治疗中的应用显著增加,尤其是与化疗联合应用时。相当一部分患者接受单纯化疗。