Abstract

BackgroundInterstitial 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.MethodsBetween 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.ResultsThirty-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.ConclusionsThis 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.

Highlights

  • Interstitial lung diseases induced by anticancer agents (ILD-AA) are rare adverse effects of anticancer therapy

  • The incidence of interstitial lung disease (ILD)-AA has been reported to be more than 20% in patients with a usual interstitial pneumonia pattern identified on high resolution computed tomography (HRCT) [1, 6]

  • We aimed to investigate the relationships among serum biomarkers, including Krebs von den Lungen-6 (KL-6) and surfactant protein D (SP-D), the patterns of ILD-AA as assessed using HRCT scans, and the prognosis of patients with advanced lung cancer

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Summary

Introduction

Interstitial lung diseases induced by anticancer agents (ILD-AA) are rare adverse effects of anticancer therapy. Prognostic biomarkers for ILD-AA have not been identified in patients with advanced lung cancer. Drug-induced interstitial lung disease (D-ILD) is one of the most common adverse events caused by anticancer agents. If patients develop interstitial lung disease (ILD) induced by anticancer agents (ILDAA), clinicians cannot continue using the same anticancer agents to treat these patients. The incidence of ILD-AA has been reported to be 1% to 5% for several anticancer agents [4,5,6]. The incidence of ILD-AA has been reported to be more than 20% in patients with a usual interstitial pneumonia pattern identified on HRCT [1, 6]

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