Nivolumab for advanced non-small cell lung cancer patients with mild idiopathic interstitial pneumonia: A multicenter, open-label single-arm phase II trial

医学 特发性间质性肺炎 无容量 临床终点 肺炎 内科学 肺癌 寻常性间质性肺炎 不利影响 间质性肺病 特发性肺纤维化 多中心试验 临床试验 肿瘤科 外科 癌症 随机对照试验 多中心研究 免疫疗法
作者
Daichi Fujimoto,Makiko Yomota,Akimasa Sekine,Mitsunori Morita,Takeshi Morimoto,Yukio Hosomi,Takashi Ogura,Haruaki Tomioka,Keisuke Tomii
出处
期刊:Lung Cancer [Elsevier]
卷期号:134: 274-278 被引量:57
标识
DOI:10.1016/j.lungcan.2019.06.001
摘要

Objectives The efficacy of nivolumab against metastatic non-small cell lung cancer (NSCLC) has been demonstrated; however, pneumonitis is relatively common and is a potentially life-threatening immune-related adverse event. Patients with idiopathic interstitial pneumonia (IIP) have a higher risk of pneumonitis and are generally excluded from clinical trials. Additionally, to date, a multicenter prospective trial for previously-treated NSCLC patients with IIP has not been performed. To fulfill this unmet medical need, we conducted a multicenter, open-label single-arm phase II trial to evaluate the efficacy and safety of nivolumab in NSCLC patients with mild IIP. Materials and methods Eligible patients had previously-treated, inoperable NSCLC with mild IIPs. Mild IIP was defined as a predicted vital capacity of at least 80% and possible usual interstitial pneumonia (UIP) or inconsistent with UIP pattern by chest high-resolution computed tomography. Primary end point was the 6 months PFS rate and secondary end point was the safety of this therapy. Results Eighteen patients were enrolled in this trial. Six months PFS rate was 56%, response rate was 39%, and disease control rate was 72%. There were no treatment-related deaths. One drug-related grade 3/4 nonhematologic event (grade 3 neurotoxicity) was observed. Two patients had grade 2 pneumonitis which improved by corticosteroid therapy. Conclusions Nivolumab could be an effective therapy for NSCLC patients with mild IIPs.
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