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Nephrotoxicity of targeted therapy used to treat lung cancer.
Li, Qiuling; Lin, Jieshan; Hao, Guojun; Xie, Aihua; Liu, Shuangxin; Tang, Bin.
Afiliación
  • Li Q; Department of Nephrology, Blood Purification Center, Zhongshan People's Hospital, Zhongshan, China.
  • Lin J; Department of Nephrology, Blood Purification Center, Zhongshan People's Hospital, Zhongshan, China.
  • Hao G; Department of Nephrology, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, China.
  • Xie A; Department of Nephrology, Blood Purification Center, Zhongshan People's Hospital, Zhongshan, China.
  • Liu S; Department of Nephrology, Blood Purification Center, Zhongshan People's Hospital, Zhongshan, China.
  • Tang B; Department of Nephrology, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, China.
Front Immunol ; 15: 1369118, 2024.
Article en En | MEDLINE | ID: mdl-39026680
ABSTRACT
Lung cancer is the leading cause of cancer-related death worldwide, especially non-small cell lung cancer. Early diagnosis and better treatment choices have already provided a more promising prognosis for cancer patients. In targeted therapy, antagonists target specific genes supporting cancer growth, proliferation and metastasis. With the incorporation of targeted therapies in routine cancer therapy, it is imperative that the array of toxicities associated with these agents must be well-recognized and managed, especially since these toxicities are distinct from those seen with conventional cytotoxic agents. Drug-related nephrotoxicity has attracted attention when initiating cancer therapy. Our review aims to summarize the adverse renal effects caused by targeted therapy during lung cancer treatment, mainly focusing on EGFR and ALK tyrosine kinase inhibitors. Also, we discuss the possible mechanism of the side effect and provide managements to help improve the renal function in clinical practice.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inhibidores de Proteínas Quinasas / Terapia Molecular Dirigida / Neoplasias Pulmonares / Antineoplásicos Límite: Animals / Humans Idioma: En Revista: Front Immunol Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inhibidores de Proteínas Quinasas / Terapia Molecular Dirigida / Neoplasias Pulmonares / Antineoplásicos Límite: Animals / Humans Idioma: En Revista: Front Immunol Año: 2024 Tipo del documento: Article País de afiliación: China