摘要
目的研究吉非替尼与含铂类化疗联合时序对EGFR基因突变型肺腺癌患者的临床疗效及安全性。方法将初治的EGFR基因突变的晚期肺腺癌患者126例按照联合时序不同分为(Gef+MP)组和(MP+Gef)组。Gef+MP组患者接受吉非替尼序贯培美曲塞+顺铂方案化疗,MP+Gef组患者接受培美曲塞+顺铂序贯吉非替尼方案化疗。对比2组患者的客观缓解率(ORR)、疾病控制率(DCR)和3年无进展生存期(PFS),对比2组患者不良反应发生情况。结果 MP+Gef组ORR和DCR显著高于Gef+MP组(78.69%vs 60.00%,P<0.05;90.16%vs 72.31%,P<0.05)。MP+Gef组中位PFS显著高于Gef+MP组(18.9 vs 9.9,P<0.05)。MP+Gef组的恶心、腹泻、疲劳、呕吐等不良反应的发生率显著低于Gef+MP组(P<0.05),其他不良反应发生率无统计学差异(P>0.05)。结论 MP方案序贯吉非替尼可以显著改善EGFR基因突变晚期肺腺癌患者的ORR和DCR,提高患者的PFS,且不良反应较少且轻。
Objective To study the clinical efficacy and safety of gefitinib and platinum-containing chemotherapy for patients with mutant EGFR advanced lung adenocarcinoma. Methods 126 patients with advanced lung adenocarcinoma with mutant EGFR gene were divided into Gef + MP group and MP + Gef group according to the combined timing. Patients in the Gef + MP group received chemotherapy with gefitinib sequentially with pemetrexed + cisplatin,while patients in the MP + Gef group received chemotherapy with pemetrexed + cisplatin sequentially with gefitinib. Compared the objective response rate( ORR),the disease control rate( DCR),Progression-Free Survival( PFS) and the adverse reactions between the 2 groups. Results The ORR and DCR of MP + Gef group were significantly higher than those of Gef + MP group( 78. 69% vs 60. 00%,P 〈 0. 05; 90. 16% vs72. 31%,P 〈 0. 05). The median PFS of MP + Gef group was significantly higher than that of Gef + MP group( 18. 9 vs 9. 9,P 〈 0. 05). The incidence of adverse reactions of MP + Gef group were significantly lower than those of Gef + MP group( P 〈0. 05),such as nausea,diarrhea,fatigue and vomiting etc. Other adverse reactions had no significant difference( P 〉 0. 05). Conclusion MP combined with gefitinib can significantly improve ORR and DCR in patients with advanced lung adenocarcinoma of EGFR mutations and improve PFS with minimal and less adverse effects.
作者
陈越平
CHEN Yueping(The Second People's Hospital of Chengdu,Chengdu,610017)
出处
《实用癌症杂志》
2018年第6期927-930,共4页
The Practical Journal of Cancer