摘要
目的:本研究通过EGFR-TKI和EGFR单克隆抗体联合应用探讨治疗EGFR突变阴性和EGFR T790M突变继发性耐药的NSCLC的疗效。方法:应用EGFR突变阴性和EGFR T790M突变继发性耐药的NSCLL细胞原代培养及药敏技术检验EGFR-TKI和EGFR单克隆抗体联合应用的疗效。结果:检测厄洛替尼和西妥昔单抗联合处理对于15例EGFR突变阴性和8例T790M突变阳性的继发性耐药的NSCLC患者原代细胞的影响,应用浓度分别为50μg/mL西妥昔单抗和1μM厄洛替尼作用于EGFR突变阴性的NSCLC患者原代细胞,结果显示这三组间T/C值无显著性差异(p>0.05),对于T790M突变阳性的继发性耐药的NSCLC原代细胞这三组间T/C值有显著性差异(P<0.05),联合用药组疗效明显高于单药组。结论:进一步验证了厄洛替尼和西妥昔单抗联合应用对于EGFR突变阴性的NSCLC患者无效,但对于T790M突变阳性的继发性耐药的NSCLC患者有效。
Objective: To investigate if the combination of erlotinib and cetuximab can overcome drug resistance in N SCLC with the T790M mutation and enhance the effects in NSCLC without somatic mutations in their epidermal growth factor receptors ( EGFR ). Methods: The effects of the combination of erlotinib and cetuximab in the primary NSCLC cells with the T790M and L858R mutations and without somatic mutations in their EGFR were investigated. Results: The effects of the combination of cetuximab and erlotinib on the growth of EGFR TKI-resistant primary NSCLC cells with T790M mutation and without EGFR mutation suspension in vitro were in- vestigated. The combination had a more pronounced growth inhibition than the single-agent treatment in the primary NSCLC cells with T790M mutation ( P 〈 0.05 ), but not in the primary NSCLC cells without EGFR mutation. Conclusion: The current date data suggest that the combination of erlotinib and cetuximab is an effective strategy for the treatment of patients with EGFR TKI-resistant NSCLC and indicate combined EGFR targeting as a clinically exploitable strategy.
出处
《中国肿瘤临床》
CAS
CSCD
北大核心
2011年第24期1505-1509,共5页
Chinese Journal of Clinical Oncology