埃罗替尼
奥西默替尼
T790米
贝伐单抗
肺癌
癌症研究
血管生成
酪氨酸激酶
盐酸厄洛替尼
医学
催眠药
酪氨酸激酶抑制剂
临床试验
表皮生长因子受体
吉非替尼
癌症
肿瘤科
内科学
化疗
受体
作者
R. Motta,Gonzalo Recondo,Andrés F. Cardona,Luis Corrales,Veronica Y Arnao,Virgilio E. Failoc‐Rojas,Carlos Aliaga
标识
DOI:10.1016/j.critrevonc.2024.104294
摘要
Tyrosine kinase inhibitors (TKIs) are the standard treatment for epidermal growth factor receptor mutant (EGFRm) advanced non-small cell lung cancer (NSCLC). Combining TKIs with an angiogenesis inhibitor has shown promise in pre-clinical studies. A systematic search of clinical trials found that combining erlotinib (a first-generation TKI) with bevacizumab or ramucirumab (angiogenesis inhibitors) improved progression-free survival (PFS) in EGFRm advanced NSCLC patients compared to TKI alone. However, no significant benefit in overall survival (OS) was observed in trials. Similar efficacy was seen in patients with specific EGFR mutations. Third generation TKIs were used as second-line therapy for patients with the T790M mutation. The combination treatment was associated with a higher incidence of severe adverse events. Overall, combining erlotinib or another TKI with an angiogenesis inhibitor is a safe and effective alternative for first-line treatment in EGFRm advanced NSCLC, particularly in countries without access to osimertinib and for patients with the EGFR L858R mutation.
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