Medical Oncology, Ataturk Chest Disease and Chest Surgery Training and Reseasch Hospital, Ankara, Turkey.
Ankara Yildirim Beyazit University, Ankara, Turkey.
J Cancer Res Clin Oncol. 2021 Jul;147(7):2145-2152. doi: 10.1007/s00432-020-03501-6. Epub 2021 Jan 12.
The new second-generation tyrosine kinase inhibitors (TKIs) have superior survival outcome and worse toxicity profile when compared with first-generation TKIs according to the results of clinical trials. However, there are limited studies that investigate the efficacy and safety of the new generation TKIs in real-world patients. Thus, we aimed to compare the efficacy and safety of the afatinib, an irreversible inhibitor of ErbB family receptor, and first-generation TKIs in real-world patients.
We included advanced nonsmall cell lung cancer (NSCLC) patients who had EGFR exon 19del mutation and treated with afatinib or first-generation TKIs as upfront treatment between 2016 and 2020. All patient's information was collected retrospectively. The study cohort was divided as afatinib arm and erlotinib/gefitinib arm.
A total of 283 patients at the 24 oncology centers were included. The 89 and 193 of whom were treated with afatinib and erlotinib/gefitinib, respectively. After 12.9 months (mo) of follow-up, the median PFS was statistically longer in the afatinib arm than erlotinib/gefitinib arm (19.3 mo vs. 11.9 mo, p: 0.046) and the survival advantage was more profound in younger patients (< 65 years). The 24-mo overall survival rate was 76.1% and 49.5% in the afatinib arm and erlotinib/gefitinib arm, respectively. Although all-grade adverse event (AE) rates were similar between the two arms, grade 3-4 AE rates were higher in the afatinib arm (30.7% vs. 15.2%; p: 0.004).
In our real-world study, afatinib has superior survival outcomes despite worse toxicity profile as inconsistent with clinical study results and it is the good upfront treatment option for younger patients and elderly patients who have good performance status.
根据临床试验结果,新型第二代酪氨酸激酶抑制剂(TKI)的生存结果优于第一代 TKI,但其毒性谱更差。然而,目前有限的研究调查了新型 TKI 在真实世界患者中的疗效和安全性。因此,我们旨在比较不可逆的 ErbB 家族受体抑制剂阿法替尼和第一代 TKI 在真实世界患者中的疗效和安全性。
我们纳入了 2016 年至 2020 年间接受阿法替尼或第一代 TKI 作为一线治疗的 EGFR 外显子 19 缺失突变的晚期非小细胞肺癌(NSCLC)患者。所有患者的信息均采用回顾性收集。研究队列分为阿法替尼组和厄洛替尼/吉非替尼组。
共有 283 名患者来自 24 个肿瘤中心,其中 89 名和 193 名患者分别接受了阿法替尼和厄洛替尼/吉非替尼治疗。在随访 12.9 个月(mo)后,阿法替尼组的中位无进展生存期(PFS)明显长于厄洛替尼/吉非替尼组(19.3 mo 比 11.9 mo,p:0.046),在年轻患者(<65 岁)中生存优势更为显著。阿法替尼组和厄洛替尼/吉非替尼组的 24 个月总生存率分别为 76.1%和 49.5%。尽管两组的所有级别不良事件(AE)发生率相似,但阿法替尼组的 3-4 级 AE 发生率更高(30.7%比 15.2%;p:0.004)。
在我们的真实世界研究中,阿法替尼的生存结果优于毒性谱较差的第一代 TKI,这与临床研究结果不一致,对于年轻患者和体能状态良好的老年患者,阿法替尼是一种较好的一线治疗选择。