Department of Experimental Therapeutics, National Cancer Center Hospital, 5 Chome-1-1 Tsukiji, Tokyo, Japan.
Department of Thoracic Oncology, Hyogo Cancer Center, Akashi, Japan.
Invest New Drugs. 2024 Jun;42(3):261-271. doi: 10.1007/s10637-024-01422-6. Epub 2024 Mar 26.
Pembrolizumab plus epacadostat (indoleamine 2,3-dioxygenase-1 inhibitor) was well tolerated in Japanese patients with advanced solid tumors in part A of the nonrandomized, open-label, phase 1 KEYNOTE-434 study (NCT02862457). We report results from part B, which evaluated epacadostat plus pembrolizumab and chemotherapy in Japanese patients with advanced non-small-cell lung cancer (NSCLC).
Eligible patients aged ≥ 20 years had histologically or cytologically confirmed stage IIIB or IV NSCLC with no prior systemic therapy, and ECOG performance status of 0 or 1. Patients received epacadostat 100 mg orally twice-daily, pembrolizumab 200 mg intravenously every-3-weeks for ≤ 35 cycles, and 4 cycles of chemotherapy (cohort 1: cisplatin plus pemetrexed, non-squamous; cohort 2: carboplatin plus pemetrexed, non-squamous; cohort 3: carboplatin plus paclitaxel, squamous or non-squamous). Primary endpoint was incidence of dose-limiting toxicities (DLTs). Following unfavorable results from other studies, a protocol amendment removed epacadostat from the treatment combination.
Of 19 patients, 7 were enrolled in cohort 1, and 6 each in cohorts 2 and 3. Median follow-up was 13.7 (range, 4.2-27.8) months. Five of 17 (29%) DLT-evaluable patients experienced ≥ 1 DLT (cohort 1, n = 1; cohorts 2 and 3, n = 2 each); most commonly maculopapular rash (grade 3, n = 3) and increased alanine aminotransferase (grade 2, n = 1; grade 3, n = 2). All patients experienced treatment-related adverse events (AEs); 58% experienced grade 3 or 4 treatment-related AEs. Objective response rate was 47%.
The combination of epacadostat plus pembrolizumab and chemotherapy was found to be tolerable in Japanese patients with advanced NSCLC.
ClinicalTrials.gov , NCT02862457.
在 KEYNOTE-434 研究(NCT02862457)的非随机、开放标签、1 期部分 A 中,派姆单抗联合伊匹单抗(吲哚胺 2,3-双加氧酶-1 抑制剂)在日本晚期实体瘤患者中具有良好的耐受性。我们报告来自 B 部分的结果,该部分评估了伊匹单抗联合派姆单抗和化疗在日本晚期非小细胞肺癌(NSCLC)患者中的疗效。
纳入标准为年龄≥20 岁、组织学或细胞学证实的 IIIB 或 IV 期 NSCLC、无既往全身治疗、ECOG 体能状态 0 或 1。患者接受伊匹单抗 100mg 口服,每日 2 次,派姆单抗 200mg 静脉输注,每 3 周 1 次,最多 35 个周期,以及 4 个周期的化疗(队列 1:顺铂加培美曲塞,非鳞状;队列 2:卡铂加培美曲塞,非鳞状;队列 3:卡铂加紫杉醇,鳞状或非鳞状)。主要终点为剂量限制毒性(DLT)发生率。在其他研究结果不理想后,一项方案修正案将伊匹单抗从治疗组合中移除。
19 例患者中,7 例入组队列 1,6 例分别入组队列 2 和 3。中位随访时间为 13.7 个月(范围 4.2-27.8)。17 例可评估 DLT 的患者中有 5 例(4 例来自队列 1,1 例来自队列 2 和 3)发生≥1 例 DLT;最常见的是斑丘疹(3 级,n=3)和丙氨酸氨基转移酶升高(2 级,n=1;3 级,n=2)。所有患者均发生与治疗相关的不良事件(AE);58%的患者发生 3 或 4 级治疗相关 AE。客观缓解率为 47%。
在日本晚期 NSCLC 患者中,伊匹单抗联合派姆单抗和化疗的联合治疗是可以耐受的。
ClinicalTrials.gov,NCT02862457。