Division of Respirology, Neurology and Rheumatology, Department of Internal Medicine, Kurume University School of Medicine, 67 Asahi-machi, Kurume, Fukuoka, 830-0011, Japan.
Zaporizhzhya Regional Clinical Oncology Center, Zaporizhzhya State Medical University, Zaporozhye, Ukraine.
BMC Cancer. 2024 Jul 25;23(Suppl 1):1251. doi: 10.1186/s12885-023-11203-8.
Pembrolizumab is a first-line therapy for certain patients with advanced/metastatic non-small cell lung cancer (NSCLC). Combining pembrolizumab with other immunotherapies may enhance tumor cell killing and clinical outcomes. Epacadostat is a selective inhibitor of indoleamine 2,3-dioxygenase 1, an immuno-regulatory enzyme involved in tryptophan to kynurenine metabolism that inhibits T cell-mediated immune responses.
In this randomized phase II study, patients with metastatic NSCLC expressing high (≥ 50%) programmed death-ligand 1 (PD-L1) levels received pembrolizumab 200 mg every 21 days plus oral epacadostat 100 mg twice daily (combination) or matching placebo (control). The primary objective was objective response rate (ORR); secondary objectives were progression-free survival (PFS), overall survival (OS), duration of response (DOR) and safety/tolerability.
154 patients were randomized (77 per group). Median (range) follow-up was 6.8 months (0.1-11.4) and 7.0 months (0.2-11.9) in the combination and control groups, respectively Confirmed ORR was similar between groups (combination: 32.5%, 95% CI 22.2-44.1; control: 39.0%, 95% CI 28.0-50.8; difference: - 6.5, 95% CI - 21.5 to 8.7; 1-sided P = 0.8000). Median (range) DOR was 6.2 months (1.9 + to 6.5 +) and not reached (1.9 + to 8.6 +) in the combination and control groups, respectively. Although not formally tested, median PFS was 6.7 and 6.2 months for the combination and control groups, respectively, and median OS was not reached in either group. Circulating kynurenine levels increased from C1D1 to C2D1 (P < 0.01) in the control group and decreased from C1D1 to C2D1 (P < 0.01) in the combination group but were not normalized in most patients. The most frequent serious adverse events (AEs) (≥ 2%) were pneumonia (4.0%), anemia (2.7%), atelectasis (2.7%) and pneumonitis (2.7%) in the combination group and pneumonia (3.9%), pneumonitis (2.6%) and hypotension (2.6%) in the control group. Two deaths due to drug-related AEs were reported, both in the control group.
Addition of epacadostat to pembrolizumab therapy for PD-L1-high metastatic NSCLC was generally well tolerated but did not demonstrate an improved therapeutic effect. Evaluating higher doses of epacadostat that normalize kynurenine levels when given in combination with checkpoint inhibitors may be warranted.
ClinicalTrials.gov, NCT03322540. Registered 10/26/2017.
帕博利珠单抗是某些晚期/转移性非小细胞肺癌(NSCLC)患者的一线治疗药物。将帕博利珠单抗与其他免疫疗法联合使用可能会增强肿瘤细胞杀伤作用和临床疗效。依匹卡肽是一种吲哚胺 2,3-双加氧酶 1(IDO1)的选择性抑制剂,IDO1 是一种免疫调节酶,参与色氨酸向犬尿氨酸的代谢,可抑制 T 细胞介导的免疫反应。
在这项随机的 II 期研究中,表达高(≥50%)程序性死亡配体 1(PD-L1)水平的转移性 NSCLC 患者接受帕博利珠单抗 200mg,每 21 天一次,联合口服依匹卡肽 100mg,每日两次(联合组)或匹配的安慰剂(对照组)。主要目的是客观缓解率(ORR);次要目的是无进展生存期(PFS)、总生存期(OS)、缓解持续时间(DOR)和安全性/耐受性。
154 名患者被随机分配(每组 77 名)。联合组和对照组的中位(范围)随访时间分别为 6.8 个月(0.1-11.4)和 7.0 个月(0.2-11.9)。确认的 ORR 在两组间相似(联合组:32.5%,95%CI 22.2-44.1;对照组:39.0%,95%CI 28.0-50.8;差异:-6.5,95%CI-21.5 至 8.7;单侧 P=0.8000)。联合组和对照组的中位 DOR 分别为 6.2 个月(1.9+至 6.5+)和未达到(1.9+至 8.6+)。尽管未进行正式检验,但联合组和对照组的中位 PFS 分别为 6.7 和 6.2 个月,两组的中位 OS 均未达到。在对照组中,循环犬尿氨酸水平从 C1D1 到 C2D1 增加(P<0.01),在联合组中从 C1D1 到 C2D1 减少(P<0.01),但大多数患者未恢复正常。最常见的严重不良事件(AE)(≥2%)是肺炎(4.0%)、贫血(2.7%)、肺不张(2.7%)和肺炎(2.7%)在联合组和肺炎(3.9%)、肺炎(2.6%)和低血压(2.6%)在对照组中。报告了两例与药物相关的 AE 导致的死亡,均发生在对照组。
依匹卡肽联合帕博利珠单抗治疗 PD-L1 高转移性 NSCLC 通常耐受性良好,但并未显示出改善的治疗效果。评估在与检查点抑制剂联合使用时可使犬尿氨酸水平正常化的更高剂量的依匹卡肽可能是必要的。
ClinicalTrials.gov,NCT03322540。注册日期:2017 年 10 月 26 日。