Phase II Trial of LP-300 in Combination With Carboplatin and Pemetrexed in Never Smoker Patients With Relapsed Advanced Primary Adenocarcinoma of the Lung After Treatment With Tyrosine Kinase Inhibitors.

IF 3.3 3区 医学 Q2 ONCOLOGY
J Nicholas Bodor, Jonathan Dowell, Joseph Treat, Janakiraman Subramanian, Nihal Abdulla, Eric Lee, Kamlesh Sankhala, Chun-Hui Lee, Go Makimoto, Eisaku Miyauchi, Kartik Konduri, Hajime Asahina, Shuji Murakami, Yueh-Feng Wen, Yung-Hung Luo, Shan Yueh Chang, Reginald Ewesuedo, Jianli Zhou, Yasushi Goto
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引用次数: 0

Abstract

Introduction: Most patients with non-small cell lung cancer (NSCLC) who have never smoked possess tumors bearing tyrosine kinase oncogenes. While such tumors may exhibit robust responses to front-line tyrosine inhibitors (TKIs), disease progression is inevitable. Subsequent available therapies confer limited benefit, thus developing effective treatments for these patients remains a critical need. LP-300 is a novel compound that enhances chemotherapy sensitivity and inhibits the activity of tyrosine kinase oncogenes. Retrospective subset analyses of prior phase III studies found females and never-smokers, groups likely to have oncogene-driven tumors, obtained a considerable survival advantage with LP-300 combined with platinum-based chemotherapy as compared to chemotherapy alone. Prospective validation of these findings in patients with oncogene-driven NSCLC is needed.

Methods: The HARMONIC clinical trial, which is currently in progress, is a global, randomized, phase II study (NCT05456256) evaluating the 3-drug regimen of LP-300 with pemetrexed and carboplatin versus pemetrexed and carboplatin alone in 90 patients with advanced primary lung adenocarcinoma bearing tyrosine kinase oncogenes. Patient randomization is stratified by gender and favors the LP-300 containing arm (2-1). Patients must have tumors bearing tyrosine kinase actionable alterations (i.e. EGFR, ALK, ROS1, MET, RET, BRAF, or NTRK) and have prior TKI progression or intolerance. Primary endpoints are progression-free survival (PFS) and overall survival (OS). Secondary endpoints include objective response rate, duration of objective response, clinical benefit rate, and incidence of adverse events.

Conclusion: This phase II trial is accruing patients at sites in the U.S, Japan, and Taiwan. Patient accrual is expected to be completed in the Fall of 2026.

LP-300联合卡铂和培美曲塞治疗酪氨酸激酶抑制剂治疗后复发的晚期原发性肺腺癌从不吸烟患者的II期试验
大多数从未吸烟的非小细胞肺癌(NSCLC)患者具有携带酪氨酸激酶癌基因的肿瘤。虽然这类肿瘤可能对一线酪氨酸抑制剂(TKIs)表现出强烈的反应,但疾病进展是不可避免的。随后可用的治疗方法带来的益处有限,因此为这些患者开发有效的治疗方法仍然是一个迫切的需要。LP-300是一种新型化合物,可提高化疗敏感性,抑制酪氨酸激酶癌基因的活性。对先前III期研究的回顾性亚群分析发现,女性和从不吸烟者,可能患有癌基因驱动肿瘤的群体,与单独化疗相比,LP-300联合铂基化疗获得了相当大的生存优势。需要在癌基因驱动的非小细胞肺癌患者中对这些发现进行前瞻性验证。方法:目前正在进行的HARMONIC临床试验是一项全球随机II期研究(NCT05456256),评估LP-300联合培美曲塞和卡铂与培美曲塞和卡铂单独治疗90例携带酪氨酸激酶癌基因的晚期原发性肺腺癌患者的3药方案。患者随机分组按性别分层,并倾向于LP-300组(2-1)。患者必须患有酪氨酸激酶可动性改变的肿瘤(即EGFR、ALK、ROS1、MET、RET、BRAF或NTRK),并且既往有TKI进展或不耐受。主要终点是无进展生存期(PFS)和总生存期(OS)。次要终点包括客观缓解率、客观缓解持续时间、临床获益率和不良事件发生率。结论:该II期临床试验正在美国、日本和台湾地区积累患者。患者收益预计将于2026年秋季完成。
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来源期刊
Clinical lung cancer
Clinical lung cancer 医学-肿瘤学
CiteScore
7.00
自引率
2.80%
发文量
159
审稿时长
24 days
期刊介绍: Clinical Lung Cancer is a peer-reviewed bimonthly journal that publishes original articles describing various aspects of clinical and translational research of lung cancer. Clinical Lung Cancer is devoted to articles on detection, diagnosis, prevention, and treatment of lung cancer. The main emphasis is on recent scientific developments in all areas related to lung cancer. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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