Krebs von den Lungen-6 surveillance in immune checkpoint inhibitor-induced pneumonitis.

IF 10.3 1区 医学 Q1 IMMUNOLOGY Journal for Immunotherapy of Cancer Pub Date : 2024-12-22 DOI:10.1136/jitc-2024-010114
Ryosuke Matsukane, Shoji Nakamura, Haruna Minami, Kazuya Tsubouchi, Yasuto Yoneshima, Kojiro Hata, Sai Yasukochi, Kimitaka Suetsugu, Isamu Okamoto, Takeshi Hirota
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Abstract

Background: The immune-related adverse event (irAE), pneumonitis, is a potentially fatal complication of immune checkpoint inhibitors (ICIs). Preventing its progression is crucial, emphasizing the need for effective screening tests. We evaluated the feasibility of using Krebs von den Lungen-6 (KL-6), a marker for interstitial pneumonitis, as a screening tool for pneumonitis.

Methods: We examined 500 patients with cancer divided into two groups: those with cancer other than non-small cell lung cancer (NSCLC) (Group 1, n=382) and those with NSCLC (Group 2, n=118). KL-6 levels were monitored before and during ICI treatment and analyzed for their correlation with pneumonitis.

Results: In Group 1, 37 patients (9.7%) developed pneumonitis. KL-6 levels were significantly elevated at irAE onset (pre: 222.0 U/mL, post: 743.0 U/mL, p<0.0001). Receiver operating characteristic curve analysis showed an area under the curve (AUC) of 0.903 (sensitivity 81.1%, specificity 91.6%) with a cut-off value 1.52 times pre-KL-6 levels, indicating that KL-6 is a reliable biomarker for pneumonitis. In these patients, the KL-6 level increased regardless of pneumonitis severity and was significantly elevated in patients with both symptomatic (pre: 205.0 U/mL, post: 674.5 U/mL, p<0.0001) and asymptomatic pneumonitis (pre: 314.0 U/mL, post: 743.0 U/mL, p<0.0001) at irAE onset. After irAE treatment, KL-6 levels in steroid-responsive patients remained unchanged; however, steroid-unresponsive patients had a significant increase in KL-6 levels at 1 month (1078 U/mL, p=0.031) compared with at irAE onset (678.0 U/mL). In Group 2, 24 patients (20.3%) developed irAE pneumonitis, with KL-6 levels elevated (pre: 360.5 U/mL, post: 506.5 U/mL, p=0.029) and an AUC of 0.683, indicating that KL-6 was less reliable in patients with NSCLC.

Conclusions: KL-6 is a viable screening biomarker in ICI-induced pneumonitis, particularly in patients without NSCLC. In patients with NSCLC, the significance of KL-6 monitoring is limited as it is not effective for detecting ICI-induced pneumonitis; their treatment is typically managed by pulmonary specialists. Early detection through KL-6 monitoring facilitates timely intervention for ICI-induced pneumonitis, potentially preventing treatment interruptions and reducing the need for immunosuppressants.

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免疫检查点抑制剂诱导的肺炎中克雷布斯·冯·登·伦根-6的监测。
背景:免疫相关不良事件(irAE),肺炎,是免疫检查点抑制剂(ICIs)潜在的致命并发症。预防其发展至关重要,强调需要进行有效的筛查试验。我们评估了使用间质性肺炎标志物Krebs von den Lungen-6 (KL-6)作为肺炎筛查工具的可行性。方法:500例非小细胞肺癌(NSCLC)患者分为非小细胞肺癌组(1组,n=382)和非小细胞肺癌组(2组,n=118)。在ICI治疗前和治疗期间监测KL-6水平,并分析其与肺炎的相关性。结果:第1组37例(9.7%)发生肺炎。在irAE发病时,KL-6水平显著升高(发病前:222.0 U/mL,发病后:743.0 U/mL)。结论:KL-6是一种可行的筛查性生物标志物,尤其是在非小细胞肺癌患者中。在非小细胞肺癌患者中,KL-6监测的意义有限,因为它不能有效地检测ici引起的肺炎;他们的治疗通常由肺病专家管理。通过监测KL-6的早期发现有助于及时干预ici引起的肺炎,有可能防止治疗中断并减少对免疫抑制剂的需求。
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来源期刊
Journal for Immunotherapy of Cancer
Journal for Immunotherapy of Cancer Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
17.70
自引率
4.60%
发文量
522
审稿时长
18 weeks
期刊介绍: The Journal for ImmunoTherapy of Cancer (JITC) is a peer-reviewed publication that promotes scientific exchange and deepens knowledge in the constantly evolving fields of tumor immunology and cancer immunotherapy. With an open access format, JITC encourages widespread access to its findings. The journal covers a wide range of topics, spanning from basic science to translational and clinical research. Key areas of interest include tumor-host interactions, the intricate tumor microenvironment, animal models, the identification of predictive and prognostic immune biomarkers, groundbreaking pharmaceutical and cellular therapies, innovative vaccines, combination immune-based treatments, and the study of immune-related toxicity.
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