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Non-small cell lung cancer leptomeningeal metastases treated with intrathecal therapy plus osimertinib and temozolomide and whole-brain radiation therapy: a case report

机译:鞘内注射加奥西替尼和替莫唑胺联合全脑放疗治疗非小细胞肺癌软脑膜转移瘤:一例报告

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Rationale: Leptomeningeal metastasis (LM) is an important cause of mortality in patients with non-small?cell lung cancer (NSCLC). As the symptoms of LM and its early clinical manifestations are nonspecific, early diagnosis of LM is difficult. However, there are few treatment options for LM, which leads to a poor prognosis; thus, increased clinical attention is necessary. The effects of most systemic chemotherapies on metastatic brain tumors (brain metastases and LMs) are limited as they cannot pass the blood–brain barrier; therefore, whole-brain radiation therapy is a therapeutic option. Osimertinib is a potent and irreversible third-generation oral epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI). It binds to EGFR with high affinity when the EGFR T790M mutation is present together with sensitizing mutations. The clinical efficacy of osimertinib in NSCLC patients carrying the T790M mutation has been demonstrated in clinical trial NCT02468661. Intrathecal injection of chemotherapeutic drugs can be directed to a specific lesion. Temozolomide is one such drug, and its effect has been confirmed. Patient and interventions: We treated a 38-year-old patient with NSCLC who carried the EGFR L858R mutation. We administered a combination of oral osimertinib and oral temozolomide plus an intrathecal injection of cytarabine and whole-brain radiation therapy for symptomatic multiple brain metastases. Outcomes: The patient showed a marked response to this combination therapy. To date (after ~18 months), no recurrence or new lesions have been observed and he is asymptomatic. His disease-free survival surpasses that achieved with any monotherapy for LM. Lessons: This is the first report to demonstrate the response to combination therapy in an NSCLC patient with LM. These findings indicate the potential utility of chemotherapy combined with radiotherapy combined with targeted therapy combined with local treatment, as each treatment acts via a different mechanism, enhancing their therapeutic effects.
机译:理由:薄脑膜转移(LM)是非小细胞肺癌(NSCLC)患者死亡的重要原因。由于LM的症状及其早期临床表现是非特异性的,因此LM的早期诊断很困难。但是,LM的治疗选择很少,导致预后不良。因此,有必要增加临床关注。大多数全身化学疗法对转移性脑瘤(脑转移瘤和LM)的作用是有限的,因为它们不能通过血脑屏障。因此,全脑放射疗法是一种治疗选择。奥西替尼是一种有效且不可逆的第三代口服表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)。当EGFR T790M突变与致敏突变同时存在时,它以高亲和力与EGFR结合。在临床试验NCT02468661中已证明了奥西替尼在携带T790M突变的NSCLC患者中的临床疗效。鞘内注射化疗药物可针对特定病变。替莫唑胺是一种这样的药物,其作用已得到证实。患者和干预措施:我们治疗了一名患有EGFR L858R突变的38岁NSCLC患者。我们联合口服奥西替尼和口服替莫唑胺,鞘内注射阿糖胞苷和全脑放射疗法治疗有症状的多发性脑转移。结果:患者对该联合疗法表现出明显的反应。迄今为止(约18个月后),未观察到复发或新病变,并且他没有症状。他的无病生存期超过了任何LM单药疗法所能达到的。经验教训:这是第一份证明对患有LM的NSCLC患者对联合治疗的反应的报告。这些发现表明,化学疗法,放射疗法,靶向疗法以及局部治疗相结合的潜在效用,因为每种疗法通过不同的机制起作用,从而增强了它们的治疗效果。

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