Wood Cameron, Lyniv Liliana, Isaacs James M, Kaufman Jacob M, Oduah Eziafa I, Clarke Jeff, Crawford Jeffrey, Stinchcombe Thomas, Tong Betty C, Wang Xiaofei, Gu Lin, Wigle Dennis, Dragnev Konstantin H, Antonia Scott J, Weinhold Kent, Ready Neal
Medical Oncology, Bon Secours Richmond Health System, Kilmarnock, Virginia, USA.
Division of Medical Oncology, Duke University Health System, Durham, North Carolina, USA.
J Immunother Cancer. 2025 Feb 4;13(2):e010395. doi: 10.1136/jitc-2024-010395.
Our study was designed to determine the safety, efficacy, and immunological effects of perioperative pembrolizumab in early-stage NSCLC.
This is a single-arm phase II study of perioperative pembrolizumab in patients with untreated, clinical stage IB to IIIA NSCLC. Patients received two doses of 200 mg pembrolizumab, surgery, standard adjuvant chemotherapy, followed by four doses adjuvant pembrolizumab. The primary objective of this study was to determine surgical feasibility rate, and secondary objectives are pathological response rate, treatment adverse events, efficacy data, and exploratory analysis of biomarkers.
30 patients initiated perioperative pembrolizumab, and 25 completed tumor resection. At median follow-up of 59 months after surgical resection, seven patients had disease progression, while six had died representing. A 5-year progression-free survival (PFS) from time of surgery was 72.0% (56.4%-91.9%) and overall survival (OS) from time of surgery was 75.8% (60.7%-94.7%). Major pathological response (MPR) was found in seven tumors (28%) including two complete responses (4%). Across all treated patients, four receiving neoadjuvant and four receiving adjuvant pembrolizumab experienced treatment-related adverse events of grade 3 or higher with no grade 5 events. Plasma proprotein convertase subtilisin/kexin type 9 (PCSK9) levels increased across our patient cohort over time from baseline until postsurgery and remained elevated at the end of treatment. There was a significant difference between mean plasma PCSK9 levels for patients with MPR versus all other patients on study when checked postoperatively.
Perioperative pembrolizumab was safe and effective with promising MPR rate, PFS, and OS.
我们的研究旨在确定围手术期帕博利珠单抗在早期非小细胞肺癌(NSCLC)中的安全性、疗效和免疫效应。
这是一项针对未经治疗的临床IB期至IIIA期NSCLC患者的围手术期帕博利珠单抗单臂II期研究。患者接受两剂200mg帕博利珠单抗、手术、标准辅助化疗,随后接受四剂辅助帕博利珠单抗。本研究的主要目的是确定手术可行性率,次要目的是病理缓解率、治疗不良事件、疗效数据以及生物标志物的探索性分析。
30例患者开始围手术期使用帕博利珠单抗,25例完成肿瘤切除。手术切除后中位随访59个月时,7例患者疾病进展,6例患者死亡。从手术时间起的5年无进展生存期(PFS)为72.0%(56.4%-91.9%),从手术时间起的总生存期(OS)为75.8%(60.7%-94.7%)。在7个肿瘤(28%)中发现主要病理缓解(MPR),包括2个完全缓解(4%)。在所有接受治疗的患者中,4例接受新辅助治疗和4例接受辅助帕博利珠单抗治疗的患者发生3级或更高等级的治疗相关不良事件,无5级事件。在我们的患者队列中,血浆前蛋白转化酶枯草溶菌素/kexin 9型(PCSK9)水平从基线到术后随时间升高,并在治疗结束时保持升高。术后检查时,MPR患者与研究中的所有其他患者的平均血浆PCSK9水平存在显著差异。
围手术期帕博利珠单抗安全有效,MPR率、PFS和OS前景良好。