The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Jyoban Hospital of Tokiwa Foundation, Fukushima, Japan.
JAMA Oncol. 2018 Aug 1;4(8):1112-1115. doi: 10.1001/jamaoncol.2017.4526.
Nivolumab and epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) are now the standard-of-care therapies in non-small cell lung cancer (NSCLC). Although EGFR-TKIs are well understood and have well-defined safety profiles, our experience with immune checkpoint inhibitors is still growing, particularly regarding the use of combinations of different classes of antitumor agents, including both the concomitant and sequential use of such agents.
To determine whether nivolumab increases EGFR-TKI-associated interstitial pneumonitis (IP).
DESIGN, SETTING, AND PARTICIPANTS: A database study of 20 516 participants with NSCLC in the US Food and Drug Administration Adverse Event Reporting System (FAERS) database, performed between April 2015 and March 2017.
We compared the incidence of EGFR-TKI-associated IP in patients receiving and not receiving nivolumab treatment.
The mean (SD) age of participants treated with EGFR-TKI, with and without nivolumab, was 64.4 (15.5) and 68.9 (11.8) years, respectively, and the proportion of men was 40.0% and 53.8%, respectively. Of the 20 516 participants with NSCLC, 985 cases (4.80%; 95% CI, 4.51-5.10) developed IP. Of 5777 patients treated with EGFR-TKI, 265 developed IP (4.59%; 95% CI, 4.06-5.16). Of 70 patients treated with both EGFR-TKI and nivolumab, 18 developed IP (25.7%; 95% CI, 16.0-37.6). The adjusted odds ratio for an interaction between EGFR-TKI and nivolumab was 4.31 (95% CI, 2.37-7.86; P < .001), suggesting the existence of an interaction. When we further stratified the patients by treatment with and without nivolumab, the odds ratio of EGFR-TKI-associated IP in cases with and without nivolumab treatment was 5.09 (95% CI, 2.87-9.03) and 1.22 (95% CI, 1.00-1.47), respectively.
We found a higher proportion of reports of IP for nivolumab in combination with EGFR-TKI vs treatment with either drug alone. Owing to the limitations of this study, the results warrant further confirmation. However, careful consideration should be given to the possibility of an increased risk of IP when EGFR-TKI is administered in combination with nivolumab, including concomitant and sequential use, and careful monitoring for IP is recommended.
纳武利尤单抗和表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)现在是非小细胞肺癌(NSCLC)的标准治疗方法。虽然 EGFR-TKIs 已经得到了很好的理解,并且具有明确的安全性特征,但我们对免疫检查点抑制剂的经验仍在不断发展,特别是在使用不同类别的抗肿瘤药物联合治疗方面,包括同时和序贯使用这些药物。
确定纳武利尤单抗是否会增加 EGFR-TKI 相关的间质性肺炎(IP)。
设计、地点和参与者:这是一项在美国食品和药物管理局不良事件报告系统(FAERS)数据库中进行的 20516 名 NSCLC 患者的数据库研究,研究时间为 2015 年 4 月至 2017 年 3 月。
我们比较了接受和未接受纳武利尤单抗治疗的患者中 EGFR-TKI 相关 IP 的发生率。
接受 EGFR-TKI 治疗的患者(有和没有纳武利尤单抗)的平均(SD)年龄分别为 64.4(15.5)岁和 68.9(11.8)岁,分别有 40.0%和 53.8%的患者为男性。在 20516 名 NSCLC 患者中,985 例(4.80%;95%CI,4.51-5.10)发生了 IP。在 5777 名接受 EGFR-TKI 治疗的患者中,有 265 例发生了 IP(4.59%;95%CI,4.06-5.16)。在 70 名同时接受 EGFR-TKI 和纳武利尤单抗治疗的患者中,有 18 例发生了 IP(25.7%;95%CI,16.0-37.6)。EGFR-TKI 和纳武利尤单抗之间相互作用的调整后比值比为 4.31(95%CI,2.37-7.86;P<0.001),表明存在相互作用。当我们进一步按有无纳武利尤单抗治疗对患者进行分层时,有和无纳武利尤单抗治疗的 EGFR-TKI 相关 IP 的比值比分别为 5.09(95%CI,2.87-9.03)和 1.22(95%CI,1.00-1.47)。
我们发现纳武利尤单抗联合 EGFR-TKI 治疗的 IP 报告比例高于单独使用任何一种药物。由于这项研究的局限性,结果需要进一步证实。然而,当 EGFR-TKI 与纳武利尤单抗联合使用时,应仔细考虑 IP 风险增加的可能性,包括同时和序贯使用,并建议密切监测 IP。