Suppr超能文献

KeyPemls-004 研究方案:一项评估派姆单抗联合泊马度胺和多西他赛治疗既往接受免疫治疗(PD-1/PD-L1 抑制剂)后进展(PD)的转移性非小细胞肺癌患者的 II 期研究,包括单独用药或联合铂类双药化疗

Study protocol of KeyPemls-004: A phase 2 study of pembrolizumab in combination with plinabulin and docetaxel in previously treated patients with metastatic non-small cell lung cancer and progressive disease (PD) after immunotherapy (PD-1/PD-L1 inhibitor) alone or in combination with platinum-doublet chemotherapy.

机构信息

Department of Respiratory and Critical Care Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

Thorac Cancer. 2023 Mar;14(8):773-778. doi: 10.1111/1759-7714.14806. Epub 2023 Feb 1.

Abstract

INTRODUCTION

Immune checkpoint inhibitor (ICI)-based treatment regimens have become the standard of care for first-line treatment of metastatic epidermal growth factor receptor (EGFR)/anaplastic lymphoma kinase (ALK) wild-type non-small cell lung cancer (NSCLC). Nevertheless, most patients inevitably develop disease progression, and the mechanisms of resistance to first-line immunotherapy are not clear. ICIs in combination with agents targeting other pathways may serve as second-line therapy options. Plinabulin is a selective immunomodulating microtubule-binding agent which inhibits the polymerization of tubulin monomers, with multiple mechanisms to inhibit tumor growth. Clinical studies have demonstrated preliminary the antitumor efficacy of this agent. Therefore, we hypothesize that a combination of plinabulin with programmed death 1 (PD-1) inhibitor and docetaxel may result in higher efficacy and fewer side effects leading to better tolerance.

METHODS

In this investigator-initiated, single-arm, open-label, phase II trial, metastatic NSCLC patients who acquired resistance to first-line immunotherapy-based therapy will be enrolled. Participants will receive pembrolizumab 200 mg D1, plinabulin 30 mg/m D1 and D8, and docetaxel 75 mg/m D1 intravenously for a 21-day cycle. The study intervention will be given until disease progression, intolerable toxicity, informed consent withdrawal or investigator decision. The primary endpoint is investigator-based objective response rate per Response Evaluation Criteria in Solid Tumors, version 1.1. The secondary endpoints are progression-free survival, overall survival, duration of response, and safety.

DISCUSSION

This trial will provide evidence of the benefit and safety of pembrolizumab in combination with plinabulin and docetaxel in metastatic NSCLC patients who have been exposed and developed resistance to first-line PD-1/PD-L1 inhibitor either as monotherapy or in combination with chemotherapy.

摘要

简介

免疫检查点抑制剂(ICI)为基础的治疗方案已成为转移性表皮生长因子受体(EGFR)/间变性淋巴瘤激酶(ALK)野生型非小细胞肺癌(NSCLC)一线治疗的标准治疗方案。然而,大多数患者不可避免地会出现疾病进展,并且对一线免疫治疗的耐药机制尚不清楚。ICI 联合针对其他途径的药物可能作为二线治疗选择。普利纳布林是一种选择性免疫调节微管结合剂,可抑制微管单体的聚合,具有多种抑制肿瘤生长的机制。临床研究初步证明了该药物的抗肿瘤疗效。因此,我们假设普利纳布林与程序性死亡 1(PD-1)抑制剂和多西他赛联合使用可能会产生更高的疗效和更少的副作用,从而提高耐受性。

方法

本研究为研究者发起的、单臂、开放标签、II 期临床试验,纳入对一线免疫治疗后耐药的转移性 NSCLC 患者。参与者将接受帕博利珠单抗 200mg D1、普利纳布林 30mg/m D1 和 D8 以及多西他赛 75mg/m D1 静脉滴注,每 21 天为一个周期。研究干预将持续到疾病进展、不可耐受的毒性、知情同意书撤回或研究者决定。主要终点是根据实体瘤反应评估标准 1.1 计算的研究者评估的客观缓解率。次要终点是无进展生存期、总生存期、缓解持续时间和安全性。

讨论

该试验将为接受过一线 PD-1/PD-L1 抑制剂单药或联合化疗治疗且已发生耐药的转移性 NSCLC 患者提供使用帕博利珠单抗联合普利纳布林和多西他赛治疗的获益和安全性证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c1f/10008678/d2880649d97a/TCA-14-773-g003.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验