4.6 Article

Leptomeningeal metastasis in patients with non-small cell lung cancer after stereotactic radiosurgery for brain metastasis

期刊

JOURNAL OF NEUROSURGERY
卷 139, 期 2, 页码 385-392

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AMER ASSOC NEUROLOGICAL SURGEONS
DOI: 10.3171/2022.11.JNS221888

关键词

non-small cell lung cancer; stereotactic radiosurgery; brain metastasis; epidermal growth factor receptor; leptomeningeal metastasis; oncology

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This study analyzed the incidence and risk factors of leptomeningeal metastasis (LM) development in patients with non-small cell lung cancer (NSCLC) and brain metastases (BMs) after stereotactic radiosurgery (SRS), as well as the survival outcomes and prognostic factors after LM development. The results showed that LM developed in 13.7% of NSCLC patients after SRS treatment. Large initial tumor volume and more than 5 BM lesions were associated with LM development after SRS. Chemotherapy and targeted therapy after LM were associated with better survival in patients with LM after SRS.
OBJECTIVE Stereotactic radiosurgery (SRS) is an effective treatment for brain metastases (BMs) in patients with non-small cell lung cancer (NSCLC). However, factors associated with the development of post-SRS leptomeningeal metastasis (LM) remain unclear. The authors analyzed the incidence and risk factors of LM development in patients with NSCLC and BMs after SRS and examined the survival outcomes and prognostic factors after LM development. METHODS This retrospective study included patients with NSCLC treated with SRS for MRI-diagnosed BM from 2002 to 2021. The authors recorded various clinical and demographic data, including age, sex, tumor histology, molecular profile of tumors, extracranial disease status, previous craniotomy, Karnofsky Performance Status, systemic treatments, tumor volume, and number of BMs. The management and survival outcomes after LM diagnosis were also recorded.RESULTS LM developed in 13.7% of patients with NSCLC and BMs after SRS treatment. Large initial tumor volume and more than 5 BM lesions, but not EGFR mutation status and post-SRS treatment, were associated with LM development after SRS. Multivariate analysis revealed that chemotherapy and targeted therapy after LM were associated with better survival in patients with LM after SRS. CONCLUSIONS This study is the first to evaluate the risk factors for LM in a relatively large cohort of patients with NSCLC after SRS. In patients with BMs harboring risk factors for subsequent LM, such as initial tumor volume and num-ber of metastatic lesions, aggressive therapies with high CNS penetrating ability should be considered.

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