Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden; Theme Cancer, Medical Unit Head and Neck, Lung, and Skin Tumors, Thoracic Oncology Center, Karolinska University Hospital, Stockholm, Sweden.
Department of Respiratory Medicine, Linköping University Hospital, Linköping, Sweden.
Acta Oncol. 2024 Apr 21;63:198-205. doi: 10.2340/1651-226X.2024.20309.
The treatment landscape for patients with advanced non-small cell lung cancer (NSCLC) has evolved significantly since the introduction of immunotherapies. We here describe PD-L1 testing rates, treatment patterns, and real-world outcomes for PD-(L)1 inhibitors in Sweden.
Data were obtained from the Swedish National Lung Cancer Registry for patients with advanced NSCLC and Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-2 who initiated first-line -systemic treatment from 01 April 2017 to 30 June 2020. PD-L1 testing was available in the registry from 01 January 2018. Kaplan-Meier was used for overall survival (OS) by type treatment and histology.
A total of 2,204 patients with pathologically confirmed unresectable stage IIIB/C or IV NSCLC initiated first-line treatment, 1,807 (82%) with nonsquamous (NSQ) and 397 (18%) with SQ. Eighty-six per cent (NSQ) or 85% (SQ) had been tested for PD-L1 expression, a proportion that increased over time. The use of platinum-based therapy as first-line treatment decreased substantially over time while there was an upward trend for PD-(L)1-based therapy. Among patients with PS 0-1 initiating a first-line PD-(L)1 inhibitor monotherapy, the median OS was 18.6 and 13.3 months for NSQ and SQ NSCLC patients, respectively, while for the PD-(L)1 inhibitor and chemotherapy combination regimen, the median OS was 24.0 months for NSQ and not evaluable for SQ patients.
The majority of advanced NSCLCs in Sweden were tested for PD-L1 expression. Real-world OS in patients with PS 0-1 receiving first-line PD-(L)1 inhibitor-based regimens was similar to what has been reported in pivotal clinical trials on PD-(L)1 inhibitors.
自免疫疗法问世以来,晚期非小细胞肺癌(NSCLC)患者的治疗格局发生了重大变化。在此,我们描述了 PD-L1 检测率、治疗模式以及 PD-(L)1 抑制剂在瑞典的真实世界疗效。
从瑞典国家肺癌登记处获取了 2017 年 4 月 1 日至 2020 年 6 月 30 日期间,接受一线 -全身治疗的、组织学证实的不可切除 IIIB/C 期或 IV 期 NSCLC 且东部肿瘤协作组(ECOG)体能状态(PS)为 0-2 的患者数据。PD-L1 检测于 2018 年 1 月 1 日在登记处开放。根据治疗类型和组织学,采用 Kaplan-Meier 法计算总生存期(OS)。
共 2204 例病理证实不可切除的 IIIB/C 期或 IV 期 NSCLC 患者接受了一线治疗,其中 1807 例(82%)为非鳞状(NSQ),397 例(18%)为鳞状(SQ)。86%(NSQ)或 85%(SQ)的患者接受了 PD-L1 表达检测,且随着时间的推移,这一比例不断增加。铂类药物为基础的治疗作为一线治疗的应用比例随时间显著下降,而 PD-(L)1 为基础的治疗则呈上升趋势。在 PS 为 0-1 的患者中,接受一线 PD-(L)1 抑制剂单药治疗的患者,NSQ 和 SQ NSCLC 患者的中位 OS 分别为 18.6 个月和 13.3 个月,而 PD-(L)1 抑制剂联合化疗方案的中位 OS 分别为 24.0 个月和 SQ 患者不可评估。
瑞典的大多数晚期 NSCLC 患者都进行了 PD-L1 表达检测。PS 为 0-1 的患者接受一线 PD-(L)1 抑制剂为基础的治疗方案的真实世界 OS 与 PD-(L)1 抑制剂关键临床试验报道的结果相似。