80 毫克奥西默替尼治疗表皮生长因子受体突变阳性非小细胞肺癌相关的多器官转移患者的 II 期疗效和安全性(BLOSSOM)。

IF 42.1 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2024-08-10 Epub Date: 2024-06-03 DOI:10.1200/JCO.24.00708
Sehhoon Park, Richard Baldry, Hyun Ae Jung, Jong-Mu Sun, Se-Hoon Lee, Jin Seok Ahn, Yu Jung Kim, Youngjoo Lee, Dong-Wan Kim, Sang-We Kim, Ki Hyeong Lee, Won Jae Lee, Jung Won Choi, Kyuha Chong, Jung-Il Lee, So-Hyeon Gwon, Nak-Hoon Son, Myung-Ju Ahn
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引用次数: 0

摘要

目的:表皮生长因子受体(EGFR)突变的非小细胞肺癌(NSCLC)患者在接受第一代或第二代表皮生长因子受体酪氨酸激酶抑制剂(TKIs)治疗后,出现胸膜转移(LMs)的几率很高。这项研究评估了80毫克、每天一次的奥西美替尼对既往第一代或第二代表皮生长因子受体酪氨酸激酶抑制剂耐药的LM患者的疗效、安全性和药代动力学:在这项II期多中心、开放标签、单臂研究中,80毫克奥希替尼被用于既往接受过EGFR TKIs治疗后出现LMs的EGFR突变NSCLC患者。主要终点是总生存期(OS),由盲法独立中央审查(BICR)和第3和第6周期第一天的血浆和脑脊液(CSF)药代动力学分析评估客观反应率:共有73名确诊为LM的患者接受了奥希替尼治疗,其中包括64名可接受LM疗效评估的患者--T790M阴性(62人)和T790M阳性(2人)。完整分析组的中位OS为15.6个月(95% CI,11.5至20.2个月)。LM的客观反应率为51.6%,包括15.6%的完全反应,在LM疗效可评估组中,BICR的疾病控制率为81.3%。根据BICR,LM无进展生存期中位数为11.2个月(95% CI,7.7至15.3),应答持续时间为12.6个月(95% CI,7.6至17.7),OS为15.0个月(95% CI,11.3至18.7)。药代动力学分析显示,CSF与游离血浆中奥西替尼的比率为22%。大多数安全性为1级和2级:该研究表明,每日一次80毫克的奥希替尼对患有LMs的NSCLC患者有明显的颅内疗效和生存获益。这些数据支持将每日80毫克的奥希替尼作为表皮生长因子受体(EGFR)突变的NSCLC LMs患者的一种治疗选择,无论T790M突变状态如何。
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Phase II Efficacy and Safety of 80 mg Osimertinib in Patients With Leptomeningeal Metastases Associated With Epidermal Growth Factor Receptor Mutation-Positive Non-Small Cell Lung Cancer (BLOSSOM).

Purpose: Leptomeningeal metastases (LMs) exhibit a high incidence in patients with epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC) post-treatment with first- or second-generation EGFR tyrosine kinase inhibitors (TKIs). This investigation evaluates the efficacy, safety, and pharmacokinetics of 80 mg once daily osimertinib in patients with LMs resistant to prior first- or second-generation EGFR TKIs.

Materials and methods: In this phase II multicenter, open-label, single-arm study, 80 mg osimertinib was administered to patients with EGFR-mutated NSCLC who had developed LMs subsequent to treatment with prior EGFR TKIs. The primary end point was overall survival (OS), assessed alongside objective response rate by the blinded independent central review (BICR) and a pharmacokinetic analysis of plasma and cerebrospinal fluid (CSF) on the first day of cycles 3 and 6.

Results: A total of 73 patients diagnosed with LM were treated with osimertinib, including 64 patients evaluable for the LM efficacy set-T790M negative (n = 62) and T790M positive (n = 2). The median OS in the full-analysis set was 15.6 months (95% CI, 11.5 to 20.2). The objective response rate for LM was 51.6%, including a 15.6% complete response, and the disease control rate was 81.3% by BICR in the LM efficacy evaluable set. The median LM progression-free survival by BICR was 11.2 months (95% CI, 7.7 to 15.3), the duration of response was 12.6 months (95% CI, 7.6 to 17.7), and OS was 15.0 months (95% CI, 11.3 to 18.7). Pharmacokinetic analysis showed that the CSF to free plasma osimertinib ratio was 22%. Most safety profiles were grade 1 and 2.

Conclusion: The study demonstrates significant intracranial efficacy and survival benefits of 80 mg once daily osimertinib in NSCLC patients with LMs. The data support considering daily 80 mg of osimertinib as a treatment option for EGFR-mutated NSCLC patients with LMs, irrespective of T790M mutation status.

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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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