Overcoming refractory leptomeningeal metastasis in nonsmall cell lung cancer with intrathecal pemetrexed and osimertinib: a case report.

IF 1.8 4区 医学 Q3 ONCOLOGY
Li Xue, Xuhui Zhao, Xiaohui Tai, XuXia Zhang, Lingfang Zhang, Hongling Li
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引用次数: 0

Abstract

Leptomeningeal metastasis (LM), a devastating complication of advanced nonsmall cell lung cancer (NSCLC), severely compromises patient survival and quality of life. Currently, standardized diagnostic criteria and treatment protocols for NSCLC-associated LM remain undefined, posing significant clinical challenges. Here, we present a case of a 58-year-old female with advanced epidermal growth factor receptor (EGFR)-mutated (exon 19 deletion) lung adenocarcinoma who developed LM after failing first-line gefitinib therapy. Initial treatment with osimertinib (80 mg/day), a third-generation EGFR-tyrosine kinase inhibitor (TKI), achieved 8 months of disease control before LM progression. Cerebrospinal fluid genomic analysis revealed acquired EGFR mutations (exon19 L747-A750delins and exon18 L718Q). Combination therapy with intrathecal pemetrexed and standard-dose osimertinib temporarily alleviated neurological symptoms. Upon disease recurrence after 6 months, therapeutic intensification through increased intrathecal pemetrexed frequency and high-dose osimertinib (160 mg/day) resulted in sustained neurological improvement and prolonged survival with manageable toxicity. This case demonstrates the potential of optimized intrathecal/systemic TKI combination strategies for EGFR-mutant NSCLC with LM, providing clinical insights for this therapeutic dilemma.

包膜内培美曲塞和奥西替尼治疗难治性非小细胞肺癌轻脑膜转移1例。
轻脑膜转移(LM)是晚期非小细胞肺癌(NSCLC)的一种破坏性并发症,严重影响患者的生存和生活质量。目前,非小细胞肺癌相关LM的标准化诊断标准和治疗方案仍不明确,这给临床带来了重大挑战。在这里,我们报告了一例58岁的女性,她患有晚期表皮生长因子受体(EGFR)突变(外显子19缺失)肺腺癌,在一线吉非替尼治疗失败后发展为LM。最初使用奥西替尼(80mg /天),一种第三代egfr -酪氨酸激酶抑制剂(TKI),在LM进展之前实现了8个月的疾病控制。脑脊液基因组分析显示获得性EGFR突变(外显子19 L747-A750delins和外显子18 L718Q)。鞘内培美曲塞和标准剂量奥西替尼联合治疗可暂时缓解神经系统症状。在6个月后疾病复发时,通过增加鞘内培美曲塞频率和高剂量奥西替尼(160 mg/天)加强治疗,可以持续改善神经系统,延长生存期,毒性可控。该病例展示了优化的鞘内/全身TKI联合治疗egfr突变型NSCLC伴LM的潜力,为这一治疗困境提供了临床见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Anti-Cancer Drugs
Anti-Cancer Drugs 医学-药学
CiteScore
3.80
自引率
0.00%
发文量
244
审稿时长
3 months
期刊介绍: Anti-Cancer Drugs reports both clinical and experimental results related to anti-cancer drugs, and welcomes contributions on anti-cancer drug design, drug delivery, pharmacology, hormonal and biological modalities and chemotherapy evaluation. An internationally refereed journal devoted to the fast publication of innovative investigations on therapeutic agents against cancer, Anti-Cancer Drugs aims to stimulate and report research on both toxic and non-toxic anti-cancer agents. Consequently, the scope on the journal will cover both conventional cytotoxic chemotherapy and hormonal or biological response modalities such as interleukins and immunotherapy. Submitted articles undergo a preliminary review by the editor. Some articles may be returned to authors without further consideration. Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool.
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