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一项关于ERK抑制剂MK-8353联合帕博利珠单抗治疗晚期实体瘤患者的1b期研究。

A phase 1b study of the ERK inhibitor MK-8353 plus pembrolizumab in patients with advanced solid tumors.

作者信息

Lakhani Nehal J, Burris Howard, Miller Wilson H, Huang Mo, Chen Lin-Chi, Siu Lillian L

机构信息

START Midwest, Grand Rapids, MI, USA.

Sarah Cannon Research Institute, Nashville, TN, USA.

出版信息

Invest New Drugs. 2024 Oct;42(5):581-589. doi: 10.1007/s10637-024-01461-z. Epub 2024 Sep 14.

Abstract

Combining a checkpoint inhibitor with an inhibitor of extracellular signal-regulated kinase (ERK) may result in synergistic antitumor activity. We evaluated MK-8353, an ERK1 and ERK2 inhibitor, plus pembrolizumab in a phase 1b study in patients with advanced solid tumors. This open-label, nonrandomized, dose-escalation study (NCT02972034) enrolled adults with advanced solid tumors previously treated with 1‒5 prior lines of therapy. MK-8353 was administered orally in combination with pembrolizumab 200 mg every 3 weeks as follows: twice daily (arm A; MK-8353 50‒350 mg), once daily (arm B; MK-8353 50‒600 mg), or once daily every other week (arm C; MK-8353 50‒300 mg). The primary objective was evaluation of safety via occurrence of dose-limiting toxicities (DLTs). A secondary objective was objective response by RECIST v1.1 per investigator assessment. Among 110 evaluable patients (arm A, n = 22; arm B, n = 50; arm C, n = 38), median age was 58.0 (range, 35‒79) years and 50% had received 1 or 2 prior lines of therapy. DLTs occurred in 19 patients (n = 6 [27%], n = 8 [16%], and n = 5 [13%], respectively); the most frequent was grade 3 maculopapular rash (n = 15). Grade 3/4 treatment-related AEs occurred in 35% of patients; the most common were maculopapular rash (13%) and increased lipase (5%); none were grade 5. Eight patients (7%) attained an objective response (arm B, n = 7 [complete response, n = 1; partial response, n = 6]; arm C, n = 1 [complete response]). In conclusion, MK-8353 once daily plus pembrolizumab could be administered with a manageable toxicity profile but had modest antitumor activity in patients with advanced solid tumors.

摘要

将一种检查点抑制剂与细胞外信号调节激酶(ERK)抑制剂联合使用可能会产生协同抗肿瘤活性。我们在一项针对晚期实体瘤患者的1b期研究中评估了ERK1和ERK2抑制剂MK-8353联合帕博利珠单抗的疗效。这项开放标签、非随机、剂量递增研究(NCT02972034)纳入了先前接受过1至5线治疗的晚期实体瘤成年患者。MK-8353与帕博利珠单抗200毫克每3周口服联合给药,具体如下:每日两次(A组;MK-8353 50至350毫克)、每日一次(B组;MK-8353 50至600毫克)或每隔一周每日一次(C组;MK-8353 50至300毫克)。主要目标是通过剂量限制毒性(DLT)的发生情况评估安全性。次要目标是根据研究者评估的RECIST v1.1标准评估客观缓解情况。在110例可评估患者中(A组,n = 22;B组,n = 50;C组,n = 38),中位年龄为58.0岁(范围35至79岁),50%的患者接受过1或2线先前治疗。19例患者出现DLT(分别为n = 6 [27%]、n = 8 [16%]和n = 5 [13%]);最常见的是3级斑丘疹(n = 15)。35%的患者发生3/4级治疗相关不良事件;最常见的是斑丘疹(13%)和脂肪酶升高(5%);无5级事件。8例患者(7%)获得客观缓解(B组,n = 7 [完全缓解,n = 1;部分缓解,n = 6];C组,n = 1 [完全缓解])。总之,MK-8353每日一次联合帕博利珠单抗给药时毒性可控,但对晚期实体瘤患者的抗肿瘤活性有限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af0c/11625062/5aac10d834af/10637_2024_1461_Fig1_HTML.jpg

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