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Current and future drug combination strategies based on programmed death-1/programmed death-ligand 1 inhibitors in non-small cell lung cancer / 中华医学杂志(英文版)
Chinese Medical Journal ; (24): 1780-1788, 2021.
Artigo em Inglês | WPRIM | ID: wpr-887589
ABSTRACT
In recent years, immune checkpoint inhibitors (ICIs) have made breakthroughs in the field of lung cancer and have become a focal point for research. Programmed death-1 (PD-1) or programmed death-ligand 1 (PD-L1) inhibitor monotherapy was the first to break the treatment pattern for non-small cell lung cancer (NSCLC). However, owing to the limited benefit of ICI monotherapy at the population level and its hyper-progressive phenomenon, it may not meet clinical needs. To expand the beneficial range of immunotherapy and improve its efficacy, several research strategies have adopted the use of combination immunotherapy. At present, multiple strategies, such as PD-1/PD-L1 inhibitors combined with chemotherapy, anti-angiogenic therapy, cytotoxic T-lymphocyte-associated protein 4 inhibitors, and radiotherapy, as well as combined treatment with new target drugs, have been evaluated for clinical practice. To further understand the current status and future development direction of immunotherapy, herein, we review the recent progress of ICI combination therapies for NSCLC.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Combinação de Medicamentos / Antígeno B7-H1 / Inibidores de Checkpoint Imunológico / Imunoterapia / Neoplasias Pulmonares Limite: Humanos Idioma: Inglês Revista: Chinese Medical Journal Ano de publicação: 2021 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Combinação de Medicamentos / Antígeno B7-H1 / Inibidores de Checkpoint Imunológico / Imunoterapia / Neoplasias Pulmonares Limite: Humanos Idioma: Inglês Revista: Chinese Medical Journal Ano de publicação: 2021 Tipo de documento: Artigo