从奥希替尼到先发制人的联合疗法

Q2 Medicine Oncotarget Pub Date : 2024-03-15 DOI:10.18632/oncotarget.28569
Mikhail V Blagosklonny
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引用次数: 0

摘要

在这里,我提出,与第一代TKIs相比,一线奥希替尼可延长表皮生长因子受体突变肺癌患者的中位无进展生存期(PFS),但与第一代TKIs相比,它降低了15%-20%患者的个体PFS。由于在治疗前检测出单个耐药细胞通常是不可能的,因此奥希替尼必须作为一线治疗药物用于所有患者,从而提高总体中位 PFS,但会对部分患者造成伤害。最简单的治疗方法是奥希替尼和吉非替尼的先期联合用药(PC)。与单用奥希替尼相比,综合PC(奥希替尼、阿法替尼/吉非替尼和卡帕替尼)可大幅提高80%患者的PFS,且不会对任何人造成伤害。本文还探讨了MET驱动型肺癌的PC。
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From osimertinib to preemptive combinations.

Here, I suggest that while first-line osimertinib extends median progression-free survival (PFS) in EGFR-mutant lung cancer compared to first-generation TKIs, it reduces individual PFS in 15-20% of patients compared to first-generation TKIs. Since detecting a single resistant cell before treatment is usually impossible, osimertinib must be used in all patients as a first-line treatment, raising median PFS overall but harming some. The simplest remedy is a preemptive combination (PC) of osimertinib and gefitinib. A comprehensive PC (osimertinib, afatinib/gefitinib, and capmatinib) could dramatically increase PFS for 80% of patients compared to osimertinib alone, without harming anyone. This article also explores PCs for MET-driven lung cancer.

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来源期刊
Oncotarget
Oncotarget Oncogenes-CELL BIOLOGY
CiteScore
6.60
自引率
0.00%
发文量
129
审稿时长
1.5 months
期刊介绍: Information not localized
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