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Immune checkpoint inhibitors for the treatment of non-small cell lung cancer brain metastases / 中华医学杂志(英文版)
Chinese Medical Journal ; (24): 1523-1531, 2023.
Article de En | WPRIM | ID: wpr-980918
Bibliothèque responsable: WPRO
ABSTRACT
Lung cancer has the highest risk of brain metastasis (BM) among all solid carcinomas. The emergence of BM has a significant impact on the selection of oncologic treatment for patients. Immune checkpoint inhibitors (ICIs) are the most promising treatment option for patients without druggable mutations and have been shown to improve survival in patients with non-small cell lung cancer (NSCLC) BM in clinical trials with good safety. Moreover, ICI has shown certain effects in NSCLC BM, and the overall intracranial efficacy is comparable to extracranial efficacy. However, a proportion of patients showed discordant responses in primary and metastatic lesions, suggesting that multiple mechanisms may exist underlying ICI activity in BM. According to studies pertaining to tumor immune microenvironments, ICIs may be capable of provoking immunity in situ . Meanwhile, systematic immune cells activated by ICIs can migrate into the central nervous system and exert antitumor effects. This review summarizes the present evidence for ICI treatment efficacy in NSCLC BM and proposes the possible mechanisms of ICI treatment for NSCLC BMs based on existing evidence.
Sujet(s)
Texte intégral: 1 Base de données: WPRIM Sujet principal: Tumeurs du cerveau / Carcinomes / Carcinome pulmonaire non à petites cellules / Microenvironnement tumoral / Inhibiteurs de points de contrôle immunitaires / Tumeurs du poumon Limites: Humans Langue: En Journal: Chinese Medical Journal Année: 2023 Type de document: Article
Texte intégral: 1 Base de données: WPRIM Sujet principal: Tumeurs du cerveau / Carcinomes / Carcinome pulmonaire non à petites cellules / Microenvironnement tumoral / Inhibiteurs de points de contrôle immunitaires / Tumeurs du poumon Limites: Humans Langue: En Journal: Chinese Medical Journal Année: 2023 Type de document: Article