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Progress of Bevacizumab in Malignant Pleural Effusion Caused by Non-small Cell Lung Cancer / 中国肺癌杂志
Chinese Journal of Lung Cancer ; (12): 118-124, 2019.
Artículo en Chino | WPRIM | ID: wpr-775655
ABSTRACT
Lung cancer is the most commonly diagnosed cancer worldwide. Malignant pleural effusion (MPE) caused by advanced lung cancer seriously affect the patients' quality of life and prognosis. The management of MPE includes thoracentesis, pleurodesis, indwelling pleural catheters and drug perfusion in pleural cavity. Vascular endothelial growth factor (VEGF) and its receptor are a group of important ligands and receptors that affect angiogenesis. They are the main factors controlling angiogenesis, and they play an important role in the formation of MPE. Bevacizumab is a recombinant humanized VEGF monoclonal antibody, competitively binding to endogenous VEGF receptor. Bevacizumab can inhibit new blood vessel formation, reduce vascular permeability, prevent pleural effusion accumulation and slow the growth of cancers. This review aims to discuss the progress of bevacizumab in the treatment of MPE caused by non-small cell lung cancer (NSCLC), and explore the clinical application, efficacy, safety and future direction of bevacizumab.
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Asunto(s)

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Patología / Neoplasias Pleurales / Derrame Pleural Maligno / Carcinoma de Pulmón de Células no Pequeñas / Usos Terapéuticos / Quimioterapia / Antineoplásicos Inmunológicos / Antineoplásicos Tipo de estudio: Estudio pronóstico Límite: Humanos Idioma: Chino Revista: Chinese Journal of Lung Cancer Año: 2019 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Patología / Neoplasias Pleurales / Derrame Pleural Maligno / Carcinoma de Pulmón de Células no Pequeñas / Usos Terapéuticos / Quimioterapia / Antineoplásicos Inmunológicos / Antineoplásicos Tipo de estudio: Estudio pronóstico Límite: Humanos Idioma: Chino Revista: Chinese Journal of Lung Cancer Año: 2019 Tipo del documento: Artículo