Wang Chunsheng, Zhao Kewei, Hu Shanliang, Li Minghuan, Song Yipeng
Department of Radiation, Yantai Yuhuangding Hospital, Yantai, China.
Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong University, Jinan, China.
Front Oncol. 2021 Mar 2;11:600844. doi: 10.3389/fonc.2021.600844. eCollection 2021.
Osimertinib resistance is inevitable. The purpose of this study was to explore the predictive value of pretreatment clinical characteristics in T790M-positive non-small cell lung cancer NSCLC patients for the resistance pattern of osimertinib during tumor progression as well as the treatment strategy.
We performed a literature search in the NCBI PubMed database to identify relevant articles and completed a pooled analysis based on 29 related published studies. The relationship between clinical characteristics, EGFR mutation type, previous treatment history and the gene mutation pattern at resistance to osimertinib was analyzed.
A total of 38 patients were included in the pooled analysis. Patients with an initial epidermal growth factor receptor EGFR mutation status of 19 deletions were more likely to have T790M loss (HR: 12.187, 95% CI: 2.186-67.945, p = 0.004). Patients with an initial EGFR mutation of L858R were more likely to have C797S mutations (HR: 0.063, 95% CI: 0.011-0.377, p = 0.002). The other factors (age, gender, ethnicity, smoking history, previous EGFR-TKI targeted therapy history, history of radiotherapy and chemotherapy) were not associated with the resistance pattern of osimertinib (all p > 0.05).
The type of EFGR mutation in T790M-positive NSCLC patients prior to treatment can predict the resistance pattern to osimertinib. This finding plays a vital role and theoretical basis in guiding clinicians to formulate treatment strategies at the early stage of treatment and rationally combine drugs to overcome EGFR-TKI resistance.
奥希替尼耐药不可避免。本研究旨在探讨T790M阳性非小细胞肺癌(NSCLC)患者治疗前临床特征对肿瘤进展过程中奥希替尼耐药模式的预测价值以及治疗策略。
我们在NCBI PubMed数据库中进行文献检索以识别相关文章,并基于29项相关已发表研究完成了一项汇总分析。分析了临床特征、表皮生长因子受体(EGFR)突变类型、既往治疗史与奥希替尼耐药时基因突变模式之间的关系。
汇总分析共纳入38例患者。初始表皮生长因子受体(EGFR)突变状态为19号外显子缺失的患者更易发生T790M缺失(风险比:12.187,95%置信区间:2.186 - 67.945,p = 0.004)。初始EGFR突变为L858R的患者更易发生C797S突变(风险比:0.063,95%置信区间:0.011 - 0.377,p = 0.002)。其他因素(年龄、性别、种族、吸烟史、既往EGFR - TKI靶向治疗史、放疗和化疗史)与奥希替尼耐药模式无关(所有p > 0.05)。
T790M阳性NSCLC患者治疗前的EGFR突变类型可预测对奥希替尼的耐药模式。这一发现对指导临床医生在治疗早期制定治疗策略以及合理联合用药以克服EGFR - TKI耐药具有至关重要的作用和理论依据。