Alanen Virve, Iivanainen Sanna, Arffman Martti, Koivunen Jussi Pekka
Oncology and Radiotherapy, Pohjois-Pohjanmaan Sairaanhoitopiiri, Oulu, Finland; MRC Oulu, Oulu University, Oulu, Finland.
National Institute for Health and Welfare, Helsinki, Finland.
ESMO Open. 2020 Oct;5(5):e000864. doi: 10.1136/esmoopen-2020-000864.
With the first and second-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs), clinical benefit and rash correlate together. EGFR TKI-induced rash can be alleviated with tetracyclines, but it is unknown whether the use of tetracyclines can increase the survival of non-small-cell lung cancer (NSCLC) patients treated with EGFR TKIs.
We collected all the patients (n=1271) who had reimbursement for EGFR TKIs (gefitinib, erlotinib and afatinib) in Finland 2011-2016, had purchased TKIs, and had data available at nationwide cancer registry. The survival was analysed from the first EGFR TKI purchase to death or end-of follow-up, and patients were stratified according to TKIs, purchases of antibiotics, their ATC class and timing.
802 (63.1%) patients had antibiotic purchases -14 to +200 days from the first EGFR TKI purchase, 447 of these tetracyclines. 322 (25.3%) had had purchased antibiotics -14 to +14 days (prophylaxis) from the first EGFR TKI purchase, 188 of these tetracyclines. Purchase of antibiotics was associated with improved survival (HR 0.80, 95% CI 0.71 to 0.91), which limited to tetracycline purchases only (HR 0.72, 95% CI 0.64 to 0.82). The largest survival benefit was seen with the prophylactic use of tetracyclines (HR 0.74, 95% CI 0.62 to 0.88). The benefit from tetracyclines was limited to erlotinib only (HR 0.68, 95% CI 0.58 to 0.78) which was retained in multivariate analysis. Prophylactic use of tetracyclines was associated with a longer erlotinib treatment duration (HR 0.81, 95% CI 0.61 to 0.96) but not with dose reductions or treatment breaks.
Tetracyclines improve the survival of NSCLC patients treated with the first and second-generation EGFR TKIs and they should be considered as a prophylaxis when initiating EGFR TKIs with high incidence of rash.
在第一代和第二代表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKIs)治疗中,临床获益与皮疹相关。EGFR TKI引起的皮疹可用四环素缓解,但使用四环素是否能提高接受EGFR TKIs治疗的非小细胞肺癌(NSCLC)患者的生存率尚不清楚。
我们收集了2011年至2016年在芬兰报销过EGFR TKIs(吉非替尼、厄洛替尼和阿法替尼)、购买过TKIs且在全国癌症登记处有可用数据的所有患者(n = 1271)。从首次购买EGFR TKI至死亡或随访结束分析生存率,并根据TKIs、抗生素购买情况、其解剖治疗化学(ATC)分类和时间进行分层。
802名(63.1%)患者在首次购买EGFR TKI后的 - 14至 + 200天内购买了抗生素,其中447人购买了四环素。322名(25.3%)患者在首次购买EGFR TKI后的 - 14至 + 14天内(预防性)购买了抗生素,其中188人购买了四环素。购买抗生素与生存率提高相关(风险比[HR] 0.80,95%置信区间[CI] 0.71至0.91),这仅限于购买四环素的患者(HR 0.72,95% CI 0.64至0.82)。预防性使用四环素观察到最大的生存获益(HR 0.74,95% CI 0.62至0.88)。四环素的获益仅限于厄洛替尼(HR 0.68,95% CI 0.58至0.78),在多变量分析中仍然存在。预防性使用四环素与厄洛替尼治疗持续时间延长相关(HR 0.81,95% CI 0.61至0.96),但与剂量减少或治疗中断无关。
四环素可提高接受第一代和第二代EGFR TKIs治疗的NSCLC患者的生存率,在开始使用皮疹发生率高的EGFR TKIs时应考虑将其作为预防措施。