Tian Ruifen, Guo Yi, Zhang Xing, Zhang Xia, Song Xia
Ruifen Tian, Department of Respiratory Medicine, Shanxi Tumour Hospital, 3 Zhigongxin Village, Taiyuan, Shanxi Province 030013, P.R. China.
Yi Guo, Department of Respiratory Medicine, Shanxi Tumour Hospital, 3 Zhigongxin Village, Taiyuan, Shanxi Province 030013, P.R. China.
Pak J Med Sci. 2024 Sep;40(8):1714-1718. doi: 10.12669/pjms.40.8.9682.
To evaluate the efficacy and safety of Apatinib combined with epidermal growth factor receptor - tyrosine kinase inhibitor (EGFR-TKI) in the treatment of patients with non-small cell lung cancer (NSCLC) and acquired EGFR-TKI resistance.
Clinical records of 106 patients with NSCLC at Shanxi Tumor Hospital of the Chinese Academy of Medical Sciences Cancer Hospital from January 2017 to October 2020, with acquired drug resistance after EGFR-TKI treatment were retrospectively analyzed. Among them, 52 patients received Apatinib combined with EGFR-TKI (Apatinib group), and 54 patients received a standard chemotherapy (pemetrexed combined with platinum) (chemotherapy group). Clinical efficacy indicators, follow-up results, and adverse reactions in both groups were compared.
There was no significant difference in the objective response rate and disease control rate between the two groups (>0.05). The progression free survival (PFS) of the Apatinib group was significantly longer than that of the chemotherapy group (10.5 months vs. 5.7 months; <0.05). There was no significant difference in adverse reactions between the two groups (>0.05).
Compared with standard chemotherapy, Apatinib combined with EGFR-TKI has the same efficacy in treating NSCLC patients with EGFR-TKI resistance, and was associated with longer PFS with no significant increase in adverse reactions.
评估阿帕替尼联合表皮生长因子受体-酪氨酸激酶抑制剂(EGFR-TKI)治疗非小细胞肺癌(NSCLC)及获得性EGFR-TKI耐药患者的疗效和安全性。
回顾性分析2017年1月至2020年10月在中国医学科学院肿瘤医院山西肿瘤医院就诊的106例NSCLC患者的临床资料,这些患者在EGFR-TKI治疗后出现获得性耐药。其中,52例患者接受阿帕替尼联合EGFR-TKI治疗(阿帕替尼组),54例患者接受标准化疗(培美曲塞联合铂类)(化疗组)。比较两组的临床疗效指标、随访结果及不良反应。
两组的客观缓解率和疾病控制率差异无统计学意义(>0.05)。阿帕替尼组的无进展生存期(PFS)显著长于化疗组(10.5个月对5.7个月;<0.05)。两组不良反应差异无统计学意义(>0.05)。
与标准化疗相比,阿帕替尼联合EGFR-TKI治疗EGFR-TKI耐药的NSCLC患者疗效相当,且PFS更长,不良反应无显著增加。