Department of Molecular and Internal Medicine, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Department of Molecular and Internal Medicine, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Respir Med. 2020 Oct;172:106131. doi: 10.1016/j.rmed.2020.106131. Epub 2020 Aug 28.
High-mobility group box 1 (HMGB1) is a pro-inflammatory protein, that is associated with tumorigenesis, interstitial lung disease (ILD), and acute lung injury. Chemotherapy-induced lung injury is a common and serious adverse event in patients with lung cancer and ILD, but its pathogenesis and predictive biomarkers are not known. This study aimed to investigate the predictive potential of serum HMGB1 levels for cytotoxic chemotherapy-induced lung injury in these patients.
From 743 patients with advanced lung cancer, we enrolled 83 consecutive patients with ILD and background-matched 83 patients without ILD. Additionally, 83 healthy subjects were included. After measuring baseline levels of serum HMGB1 in three groups, we evaluated the predictive values of baseline HMGB1 levels for cytotoxic chemotherapy-induced lung injury in patients with lung cancer and ILD.
Higher levels of serum HMGB1 were independently associated with higher tumor burden, as assessed by total tumor size, and the presence of ILD. Twenty-five (30.1%) of patients with lung cancer and ILD experienced cytotoxic chemotherapy-induced lung injury within one year. Univariate Cox proportional hazards model showed that higher levels of HMGB1 and higher tumor burden were associated with disease onset. Moreover, multivariate analysis revealed that only HMGB1 was independently associated with this severe complication in patients with lung cancer and ILD.
HMGB1 is a potential predictive blood biomarker for cytotoxic chemotherapy-induced lung injury in patients with lung cancer and ILD. This study also suggests a potential pathogenesis of this serious adverse event that tumor- and ILD-derived HMGB1 accelerates lung injury.
高迁移率族蛋白 B1(HMGB1)是一种促炎蛋白,与肿瘤发生、间质性肺病(ILD)和急性肺损伤有关。化疗引起的肺损伤是肺癌和 ILD 患者常见且严重的不良反应,但发病机制和预测生物标志物尚不清楚。本研究旨在探讨血清 HMGB1 水平对这些患者细胞毒性化疗引起的肺损伤的预测潜力。
我们从 743 例晚期肺癌患者中纳入了 83 例连续的 ILD 患者和背景匹配的 83 例无 ILD 患者。此外,还纳入了 83 例健康受试者。在三组中测量血清 HMGB1 的基线水平后,我们评估了肺癌和 ILD 患者基线 HMGB1 水平对细胞毒性化疗引起的肺损伤的预测价值。
血清 HMGB1 水平较高与较高的肿瘤负担独立相关,肿瘤总大小和 ILD 的存在也是如此。83 例肺癌和 ILD 患者中有 25 例(30.1%)在一年内发生细胞毒性化疗引起的肺损伤。单因素 Cox 比例风险模型显示,HMGB1 水平较高和肿瘤负担较高与疾病发生有关。此外,多因素分析显示,只有 HMGB1 与肺癌和 ILD 患者的这种严重并发症独立相关。
HMGB1 是肺癌和 ILD 患者细胞毒性化疗引起的肺损伤的潜在预测性血液生物标志物。本研究还提示了这种严重不良事件的潜在发病机制,即肿瘤和 ILD 来源的 HMGB1 加速了肺损伤。