Ultrasound-Guided High-Intensity Focused Ultrasound Combined With PD-1 Blockade in Patients With Liver Metastases From Lung Cancer: Protocol for a Single-Arm Phase 2 Trial.

IF 1.5 Q3 HEALTH CARE SCIENCES & SERVICES JMIR Research Protocols Pub Date : 2024-11-29 DOI:10.2196/59152
Chao Hu, Qiang Fu, Fei Fei Gao, Jian Zeng, Wei Xiao, Hui Li, Li Peng, Xi Huang, Li Yang, Wen Zhi Chen, Ming Yan Jiang
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Abstract

Background: While immunotherapy has revolutionized oncological management, its efficacy in lung cancer patients with liver metastases remains limited, potentially due to the unique immunosuppressive microenvironment of the liver. Local liver treatment has been shown to enhance the immunotherapy response, and high-intensity focused ultrasound (HIFU), a minimally invasive local treatment, has demonstrated promising results in combination with immunotherapy. However, clinical data regarding HIFU in lung cancer with liver metastases are limited.

Objective: We designed the HILL (Ultrasound-Guided High-Intensity Focused Ultrasound Combined With PD-1 Blockade in Patients With Liver Metastases From Lung Cancer) study to investigate the effectiveness and safety of HIFU in combination with immunotherapy for lung cancer with liver metastases.

Methods: The HILL study is a single-armed, single-center, phase 2 clinical trial that will enroll 30 patients with lung cancer and liver metastases. The treatment regimen involves administering HIFU to liver metastases 1 week before the first dose of a programmed cell death protein (PD)-1 blockade, which is then administered every 3 weeks. The primary aim is to determine the overall response rate based on immune-related response criteria. Secondary aims include safety, progression-free survival, overall response, overall survival, and quality of life. Exploratory studies will also be conducted using whole blood, plasma, archival cancer tissue, and tumor biopsies during progression or relapse to identify potential biomarkers.

Results: The study was funded on March 14, 2022, and received ethical approval on April 27, 2022. Clinical trial registration was completed by June 10, 2022, with participant recruitment beginning on July 10, 2022. Data collection commenced on July 14, 2022, with the enrollment of the first patient. By April 2024, 6 participants had been recruited. The results are expected to be published in December 2026.

Conclusions: This study seeks to improve treatment outcomes for lung cancer patients with liver metastases by combining HIFU and PD-1 inhibition. The study also aims to identify potential biomarkers through exploratory research that can aid in selecting patients for optimized outcomes in the future.

Trial registration: Chinese Clinical Trial Registry ChiCTR2200061076; https://www.chictr.org.cn/showproj.html?proj=170967.

International registered report identifier (irrid): DERR1-10.2196/59152.

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超声引导的高强度聚焦超声联合PD-1阻断治疗肺癌肝转移患者:单组2期试验方案
背景:虽然免疫治疗已经彻底改变了肿瘤治疗,但其对肺癌肝转移患者的疗效仍然有限,这可能是由于肝脏独特的免疫抑制微环境。局部肝脏治疗已被证明可以增强免疫治疗反应,而高强度聚焦超声(HIFU)作为一种微创局部治疗,与免疫治疗相结合已显示出有希望的结果。然而,HIFU治疗肺癌伴肝转移的临床资料有限。目的:设计HILL(超声引导高强度聚焦超声联合PD-1阻断治疗肺癌肝转移患者)研究,探讨HIFU联合免疫治疗肺癌肝转移的有效性和安全性。HILL研究是一项单臂、单中心、2期临床试验,将招募30例肺癌和肝转移患者。治疗方案包括在第一次给药程序性细胞死亡蛋白(PD)-1阻断剂前一周对肝转移灶进行HIFU治疗,然后每3周给药一次。主要目的是根据免疫相关反应标准确定总体反应率。次要目标包括安全性、无进展生存期、总反应、总生存期和生活质量。探索性研究还将在进展或复发期间使用全血、血浆、档案癌组织和肿瘤活检来确定潜在的生物标志物。结果:该研究于2022年3月14日获得资助,并于2022年4月27日获得伦理批准。临床试验注册于2022年6月10日完成,参与者招募于2022年7月10日开始。数据收集于2022年7月14日开始,纳入了第一位患者。截至2024年4月,已招募6名参与者。结果预计将于2026年12月公布。结论:本研究旨在通过HIFU联合PD-1抑制改善肺癌肝转移患者的治疗效果。该研究还旨在通过探索性研究确定潜在的生物标志物,以帮助在未来选择患者以获得最佳结果。试验注册:中国临床试验注册中心ChiCTR2200061076;https://www.chictr.org.cn/showproj.html?proj=170967.International注册报告标识符(irrid): DERR1-10.2196/59152。
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CiteScore
2.40
自引率
5.90%
发文量
414
审稿时长
12 weeks
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