Department of Respiratory Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan.
Department of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Thorac Cancer. 2022 Jan;13(2):236-246. doi: 10.1111/1759-7714.14254. Epub 2021 Dec 5.
The safety profile of systemic chemotherapy for lung cancer patients with interstitial pneumonia (IP) in clinical practice remains unclear. Using Diagnostic Procedure Combination (DPC) data from the Japanese administrative database, we investigated the mortality of hospitalized lung cancer patients with IP as they underwent a course of systemic chemotherapy nationwide.
The DPC data of patients with stage IIIB or IV lung cancer as defined by the Union for International Cancer Control Tumor-Nodes-Metastases 6th and 7th editions from April 2014 to March 2016 were obtained. Among those patients, only patients with concomitant IP and receiving systemic chemotherapy without radiotherapy were included.
Among 1524 included patients, 70 (4.6%) died in the hospital. Multivariate analysis revealed that low activities of daily living (ADL) scores on admission (hazard ratio [HR] 2.26, 95% confidence interval [CI] 1.24-4.12, p = 0.008) and high-dose corticosteroid therapy following chemotherapy (HR 2.62, 95% CI 1.44-4.77, p = 0.002) were strongly associated with in-hospital mortality. It was determined that patients possibly received high-dose corticosteroids for IP exacerbations; these patients had a higher in-hospital mortality rate of 67.7% (21/31 patients) and a significantly shorter median survival time of 55 days (95% CI 31-69 days, p < 0.001) than those who did not receive high-dose corticosteroids.
Acute exacerbation of IP treated with systemic high-dose corticosteroids is significantly associated with in-hospital mortality, and a low ADL score on admission is a risk factor for in-hospital mortality in lung cancer patients with IP who undergo systemic chemotherapy.
在临床实践中,患有间质性肺炎(IP)的肺癌患者进行全身化疗的安全性状况尚不清楚。我们利用日本行政数据库中的诊断程序组合(DPC)数据,在全国范围内调查了患有 IP 的住院肺癌患者接受全身化疗过程中的死亡率。
我们获得了第 6 版和第 7 版国际抗癌联盟肿瘤-淋巴结-转移(TNM)分期的 IIIB 或 IV 期肺癌患者的 DPC 数据。在这些患者中,仅包括同时患有 IP 并接受全身化疗而未接受放疗的患者。
在 1524 名纳入患者中,有 70 名(4.6%)在医院死亡。多变量分析显示,入院时日常生活活动(ADL)评分较低(危险比 [HR] 2.26,95%置信区间 [CI] 1.24-4.12,p=0.008)和化疗后接受大剂量皮质类固醇治疗(HR 2.62,95% CI 1.44-4.77,p=0.002)与院内死亡率密切相关。确定患者可能因 IP 恶化而接受大剂量皮质类固醇治疗;这些患者的院内死亡率更高,为 67.7%(21/31 例),中位生存时间明显更短,为 55 天(95% CI 31-69 天,p<0.001),而未接受大剂量皮质类固醇治疗的患者。
全身大剂量皮质类固醇治疗的 IP 急性加重与院内死亡率显著相关,入院时 ADL 评分较低是患有 IP 的接受全身化疗的肺癌患者院内死亡的危险因素。