Furmonertinib and intrathecal pemetrexed chemotherapy rechallenges osimertinib-refractory leptomeningeal metastasis in a non-small cell lung cancer patient harboring EGFR20 R776S, C797S, and EGFR21 L858R compound EGFR mutations: a case report.

IF 1.8 4区 医学 Q3 ONCOLOGY Anti-Cancer Drugs Pub Date : 2024-07-01 Epub Date: 2024-03-15 DOI:10.1097/CAD.0000000000001593
Guoxia Jia, Shoaib Bashir, Minting Ye, Yin Li, Mingyao Lai, Linbo Cai, Meng Xu
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引用次数: 0

Abstract

Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are considered the first-line treatment for advanced or metastatic non-small cell lung cancer (NSCLC) patients harboring EGFR mutations. However, due to the rarity of cases, the response of EGFR-TKIs in patients harboring uncommon compound EGFR mutations still needs to be determined. Here, we demonstrated the case of a 47-year-old smoker diagnosed with leptomeningeal metastasis from NSCLC and had EGFR20 R776S, C797S, and EGFR21 L858R compound mutations. He was treated with furmonertinib combined with intrathecal pemetrexed chemotherapy following progression on osimertinib, which led to clinical improvement and successfully prolonged his survival by 3 months. Regrettably, the patient eventually died from heart disease. This report provides the first reported evidence for the use of furmonertinib and intrathecal pemetrexed chemotherapy in NSCLC patients harboring EGFR R776S/C797S/L858R mutations who progressed on previous EGFR-TKIs.

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非小细胞肺癌患者携带表皮生长因子受体 20 R776S、C797S 和表皮生长因子受体 21 L858R 复合表皮生长因子受体突变,呋莫替尼和鞘内培美曲塞化疗重新挑战了奥西美替尼难治性胸膜转移:病例报告。
表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKIs)被认为是治疗EGFR突变的晚期或转移性非小细胞肺癌(NSCLC)患者的一线疗法。然而,由于病例的罕见性,EGFR-TKIs 对携带不常见的复合 EGFR 突变的患者的反应仍有待确定。这里,我们展示了一例47岁吸烟者的病例,他被诊断为NSCLC脑膜转移,且存在EGFR20 R776S、C797S和EGFR21 L858R复合突变。在奥希替尼治疗进展后,他接受了呋莫替尼联合腔内培美曲塞化疗,临床症状得到改善,并成功延长了3个月的生存期。遗憾的是,患者最终死于心脏病。该报告首次提供了证据,证明呋莫尼替尼和鞘内培美曲塞化疗适用于携带表皮生长因子受体(EGFR)R776S/C797S/L858R突变、既往服用EGFR-TKIs治疗进展的NSCLC患者。
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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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