Glasgow prognostic score for prediction of chemotherapy-triggered acute exacerbation interstitial lung disease in patients with small cell lung cancer

被引:7
|
作者
Kikuchi, Ryota [1 ]
Takoi, Hiroyuki [1 ]
Tsuji, Takao [2 ]
Nagatomo, Yoko [1 ]
Tanaka, Akane [1 ]
Kinoshita, Hayato [1 ]
Ono, Mariko [1 ]
Ishiwari, Mayuko [1 ]
Toriyama, Kazutoshi [1 ]
Kono, Yuta [1 ]
Togashi, Yuki [1 ]
Yamaguchi, Kazuhiro [1 ]
Yoshimura, Akinobu [3 ]
Abe, Shinji [1 ]
机构
[1] Tokyo Med Univ Hosp, Dept Resp Med, Tokyo, Japan
[2] Otsuki Municipal Cent Hosp, Resp Ctr, Otsuki, Japan
[3] Tokyo Med Univ Hosp, Dept Clin Oncol, Tokyo, Japan
关键词
acute exacerbation; Glasgow prognostic score; interstitial lung disease; prognosis; small cell lung cancer;
D O I
10.1111/1759-7714.13900
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Predicting the incidence of chemotherapy-triggered acute exacerbation of interstitial lung disease (AE-ILD) in patients with lung cancer is important because AE-ILD confers a poor prognosis. The Glasgow prognostic score (GPS), which is an inflammation-based index composed of serum levels of C-reactive protein and albumin, predicts prognosis in patients with small cell lung cancer (SCLC) without ILD. In this study, we investigated AE-ILD and survival outcome based on the GPS in patients with ILD associated with SCLC who were receiving chemotherapy. Methods Medical records of patients who received platinum-based first-line chemotherapy between June 2010 and May 2019 were retrospectively reviewed to compare the incidence of AE-ILD and overall survival (OS) between GPS 0, 1, and 2. Results Among our cohort of 31 patients, six (19.3%) experienced chemotherapy-triggered AE-ILD. The AE-ILD incidence increased from 9.5% to 25.0% and 50.0% with increase in GPS of 0, 1, and 2, respectively. Univariate and multivariate analyses revealed remarkable associations between GPS 2 and both AE-ILD (odds ratio for GPS 2, 18.69; p = 0.046) and prognosis (hazard ratio of GPS 2, 13.52; p = 0.002). Furthermore, median OS in the GPS 0, 1, and 2 groups was 16.2, 9.8, and 7.1 months, respectively (p < 0.001). Conclusions Our results suggest that GPS 2 is both a predictor of risk of chemotherapy-triggered AE-ILD and a prognostic indicator in patients with ILD associated with SCLC. We propose that GPS may be used as a guide to distinguish chemotherapy-tolerant patients from those at high risk of AE-ILD.
引用
收藏
页码:1681 / 1689
页数:9
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