帕米帕利作为局限期小细胞肺癌化疗后的巩固治疗:单臂开放标签2期试验

IF 3.3 2区 医学 Q2 ONCOLOGY
Jiuang Mao, Jianjiao Ni, Li Chu, Xiao Chu, Dayu Xu, Xi Yang, Zhengfei Zhu
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引用次数: 0

摘要

小细胞肺癌(SCLC)侵袭性强、预后差,由于缺乏可靶向的驱动基因组改变,其治疗一直受到阻碍。然而,由于小细胞肺癌基因组的高度不稳定性和复制压力,聚(ADP-核糖)聚合酶(PARPs)抑制剂成为研究的重点。帕米帕利(Pamiparib)是一种口服PARP1/2抑制剂,具有高选择性、强PARP捕获活性和良好的脑穿透性。利用帕米帕利作为有限分期SCLC的巩固维持治疗有望改善生存结果,并提供一种可行的治疗方法。这项单臂、开放标签 II 期试验将招募年龄在 18-75 岁、组织学/细胞学确诊的局限期 SCLC 患者,这些患者在接受以铂为基础的 cCRT 治疗后病情未见进展,且 ECOG PS 为 0 或 1。如果患者组织学确诊为混合型SCLC或NSCLC,或既往接受过肿瘤切除术,或可接受手术或立体定向体放疗/立体定向消融放疗,则将被排除在外。根据RECIST v1.1标准,参试者将在cCRT治疗后2至6周内接受帕米帕利40毫克、每天两次的治疗,每次3周,最长持续1年或直至疾病进展。主要终点是研究人员根据 RECIST v1.1 评估的 1 年无进展生存率 (PFS)。次要终点包括研究人员根据 RECIST 1.1 评估的无进展生存期、客观反应率和反应持续时间、总生存期、远处转移时间和安全性。这项研究将为帕米帕利作为LS-SCLC患者cCRT后的巩固疗法的可行性、安全性和有效性提供有价值的数据。研究还将进一步探讨疾病的分子分型或基因表达谱与治愈性反应之间的相关性。请访问 clinicaltrials.gov 网站上的 NCT05483543。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pamiparib as consolidation treatment after concurrent chemoradiotherapy of limited-stage small cell lung cancer: a single-arm, open-label phase 2 trial
Small cell lung cancer (SCLC) is highly invasive with poor prognosis, and its treatment has historically been hindered due to the absence of targetable driver genomic alterations. However, the high genomic instability and replication stress in SCLC have made poly(ADP-ribose) polymerases (PARPs) inhibitors a focus of research. Pamiparib is an orally available PARP1/2 inhibitor with high selectivity, strong PARP trapping activity, and excellent brain penetration. Utilizing pamiparib as consolidation maintenance therapy in limited-stage SCLC holds promise for improving survival outcomes and offering a viable therapeutic approach. This single-arm, open-label phase II trial will enroll patients aged 18–75 years with histologically/cytologically confirmed, limited-stage SCLC who have not progressed following definitive platinum-based cCRT and have an ECOG PS of 0 or 1. Patients will be excluded if they have histologically confirmed mixed SCLC or NSCLC, or have undergone previous tumor resection, or can be treated with surgery or stereotactic body radiation therapy/stereotactic ablative radiation therapy. Participants will receive pamiparib 40 mg twice daily every 3 weeks within 2 to 6 weeks after cCRT for up to 1 year or until disease progression according to RECIST v1.1. The primary endpoint is the 1-year progression-free survival (PFS) rate assessed by investigators per RECIST v1.1. Secondary endpoints include PFS, objective response rate, and duration of response assessed by investigators per RECIST 1.1, overall survival, time to distant metastasis, and safety. The study will provide valuable data on the feasibility, safety, and effectiveness of pamiparib as a consolidation therapy after cCRT in patients with LS-SCLC. The correlation between molecular typing or gene expression profile of the disease and curative response will be further explored. NCT05483543 at clinicaltrials.gov.
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来源期刊
Radiation Oncology
Radiation Oncology ONCOLOGY-RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
CiteScore
6.50
自引率
2.80%
发文量
181
审稿时长
3-6 weeks
期刊介绍: Radiation Oncology encompasses all aspects of research that impacts on the treatment of cancer using radiation. It publishes findings in molecular and cellular radiation biology, radiation physics, radiation technology, and clinical oncology.
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