Nakamura Kota, Kato Motoyasu, Shukuya Takehito, Mori Keita, Sekimoto Yasuhito, Ihara Hiroaki, Kanemaru Ryota, Ko Ryo, Shibayama Rina, Tajima Ken, Koyama Ryo, Shimada Naoko, Nagashima Osamu, Takahashi Fumiyuki, Sasaki Shinichi, Takahashi Kazuhisa
Department of Respiratory Medicine, Juntendo University Graduate School of Medicine, 3-1-3, Hongo, Bunkyo-ku, Tokyo, 113-8431, Japan.
Department of Respiratory Medicine, Juntendo University Urayasu Hospital, 2-1-1, Tomioka, Urayasu, Chiba, 273-0021, Japan.
BMC Cancer. 2017 May 2;17(1):302. doi: 10.1186/s12885-017-3285-6.
Interstitial lung diseases induced by anticancer agents (ILD-AA) are rare adverse effects of anticancer therapy. However, prognostic biomarkers for ILD-AA have not been identified in patients with advanced lung cancer. Our aim was to analyze the association between serum biomarkers sialylated carbohydrate antigen Krebs von den Lungen-6 (KL-6) and surfactant protein D (SP-D), and clinical characteristics in patients diagnosed with ILD-AA.
Between April 2011 and March 2016, 1224 advanced lung cancer patients received cytotoxic agents and epidermal growth factor receptor tyrosine kinase inhibitors at Juntendo University Hospital and Juntendo University Urayasu Hospital. Of these patients, those diagnosed with ILD-AA were enrolled in this case control study. ΔKL-6 and ΔSP-D were defined as the difference between the levels at the onset of ILD-AA and their respective levels prior to development of ILD-AA. We evaluated KL-6 and SP-D at the onset of ILD-AA, ΔKL-6 and ΔSP-D, the risk factors for death related to ILD-AA, the chest high resolution computed tomography (HRCT) findings, and survival time in patients diagnosed with ILD-AA.
Thirty-six patients diagnosed with ILD-AA were enrolled in this study. Among them, 14 patients died of ILD-AA. ΔSP-D in the patients who died was significantly higher than that in the patients who survived. However, ΔKL-6 did not differ significantly between the two groups. Moreover, ΔSP-D in patients who exhibited diffuse alveolar damage was significantly higher than that in the other patterns on HRCT. Receiver operating characteristic curve analysis was used to set the optimal cut off value for ΔSP-D at 398 ng/mL. Survival time for patients with high ΔSP-D (≥ 398 ng/mL) was significantly shorter than that for patients with low ΔSP-D. Multivariate analysis revealed that ΔSP-D was a significant prognostic factor of ILD-AA.
This is the first research to evaluate high ΔSP-D (≥ 398 ng/mL) in patients with ILD-AA and to determine the risk factors for ILD-AA in advanced lung cancer patients. ΔSP-D might be a serum prognostic biomarker of ILD-AA. Clinicians should evaluate serum SP-D during chemotherapy and should carefully monitor the clinical course in patients with high ΔSP-D.
抗癌药物所致间质性肺疾病(ILD-AA)是抗癌治疗罕见的不良反应。然而,晚期肺癌患者中尚未确定ILD-AA的预后生物标志物。我们的目的是分析血清生物标志物唾液酸化碳水化合物抗原克雷伯斯-冯-登-卢根-6(KL-6)和表面活性蛋白D(SP-D)与诊断为ILD-AA患者的临床特征之间的关联。
2011年4月至2016年3月期间,1224例晚期肺癌患者在顺天堂大学医院和顺天堂大学浦安医院接受了细胞毒药物和表皮生长因子受体酪氨酸激酶抑制剂治疗。在这些患者中,诊断为ILD-AA的患者被纳入本病例对照研究。ΔKL-6和ΔSP-D定义为ILD-AA发病时的水平与其在ILD-AA发生前各自水平的差值。我们评估了ILD-AA发病时的KL-6和SP-D、ΔKL-6和ΔSP-D、与ILD-AA相关的死亡危险因素、胸部高分辨率计算机断层扫描(HRCT)表现以及诊断为ILD-AA患者的生存时间。
36例诊断为ILD-AA的患者被纳入本研究。其中,14例患者死于ILD-AA。死亡患者的ΔSP-D显著高于存活患者。然而,两组之间的ΔKL-6没有显著差异。此外,HRCT表现为弥漫性肺泡损伤的患者的ΔSP-D显著高于其他类型。采用受试者工作特征曲线分析将ΔSP-D的最佳截断值设定为398 ng/mL。高ΔSP-D(≥398 ng/mL)患者的生存时间显著短于低ΔSP-D患者。多因素分析显示,ΔSP-D是ILD-AA的一个显著预后因素。
这是首次评估ILD-AA患者高ΔSP-D(≥398 ng/mL)并确定晚期肺癌患者ILD-AA危险因素的研究。ΔSP-D可能是ILD-AA的血清预后生物标志物。临床医生在化疗期间应评估血清SP-D,并应仔细监测高ΔSP-D患者的临床病程。