个体化大剂量静脉注射阿那白拉治疗COVID-19相关细胞因子风暴伴癌患者安全有效:一项回顾性匹配研究

M. Bektaş, M. Ay, M. Uyar, M. Kiliç, N. Koca, B. Ince
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引用次数: 0

摘要

背景:由于促炎细胞因子的过度释放,严重的COVID-19病程与较高的炎症状态(细胞因子风暴)相关。一些初步结果显示,COVID-19伴癌患者的疾病严重程度和死亡率更高。在本研究中,我们旨在评估大剂量静脉注射阿那白拉治疗重症和危重症伴癌患者的反应和结局。方法:本观察性回顾性研究于2021年9月1日至2022年2月1日在土耳其的一家三级转诊中心进行。研究人群分为以下两组:大剂量静脉注射阿那白组(阿那白组)和标准护理组(SoC,对照组)。Anakinra用于至少2天对类固醇治疗无反应的患者,或在入院时具有高风险和/或危重疾病的患者同时使用类固醇。结果:对146例阿那那组患者和114例对照组患者的资料进行分析。anakinra组患者年龄71(25)岁,住院时间11(12)天,对照组患者住院时间65.5(23)年,9(7.3)天。阿那金组重症57例(39%),危重68例(59.6%),危重89例(61%),危重46例(40.4%)。总体而言,anakinra组住院58例(39.7%)和25例(22%),插管52例(35.6%)和13例(11.4%),死亡54例(37%)和27例(23.7%)。阿那金组恶性肿瘤发生率为11% (n=16),对照组为7% (n=8)。在生存分析中,对照组有恶性肿瘤患者的生存率显著低于无恶性肿瘤患者(Log-Rank: p=0.002),对照组有恶性肿瘤患者的生存率显著低于阿那金组(Log-Rank: p=0.013);但anakinra组与非恶性肿瘤患者之间无差异(Log-Rank: p=0.9)。结论:在我们的研究中,恶性肿瘤患者的死亡率高于对照组,但阿那金组的死亡率高于对照组,接受阿那金组的死亡率高于SoC组。我们的研究表明静脉注射大剂量阿那白拉治疗COVID-19相关细胞因子风暴伴癌患者是安全有效的。
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Individualized High Dose Intravenous Anakinra Treatment is Safe and Effective in Patients with COVID-19 Associated Cytokine Storm Accompanying Cancer: A Retrospective Matched Study
Background: Severe COVID-19 course is associated with higher inflammatory state (cytokine storm) due to the excessive release of pro-inflammatory cytokines. Some preliminary results showed higher disease severity as well as mortality in patients with COVID-19 accompanying cancer. In this study, we aimed to evaluate the high dose intravenous anakinra treatment response and outcome in patients with severe and critically ill COVID-19 accompanying cancer. Method: This observational retrospective study was carried out at a tertiary referral center between 01.09.2021 and 01.02.2022 in Turkey. The study population consisted of two groups as follows; the patients receiving high dose intravenous anakinra (anakinra group) and the patients treated with standard of care (SoC, control group). Anakinra was started in patients who did not respond to steroid therapy at least two days or concomitantly with steroids in patients with higher risk and/or critical illness at admission. Results: Data of 146 patients in anakinra and 114 patients in control group were analyzed. Median±interquartile range (IQR) patient age was 71 (25) years, duration of hospitalization were 11 (12) days in anakinra group and 65.5 (23) years and 9 (7.3) days in control group, respectively. Fifty-seven (39 %) and 68 (59.6 %) patients had severe, 89 (61 %) and 46 (40.4 %) had critical disease in anakinra and control group, respectively. Overall, ICU admission was in 58 (39.7 %) and 25 (22 %), intubation was in 52 (35.6 %) and 13 (11.4 %) patients, 54 (37 %) and 27 (23.7 %) patients died in anakinra and control group, respectively. Malignancy frequency was 11 % (n=16) in anakinra group and 7 % (n=8) in the control group. In survival analysis, significantly lower survival rate was observed in patients with malignancy than those without in control group (Log-Rank: p=0.002) and patients with malignancy in control group compared to anakinra group (Log-Rank: p=0.013); but did not differ between patients with and without malignancy in anakinra group (Log-Rank: p=0.9). Conclusion: In our study, mortality was higher in patients with malignancy compared to those without control but not in anakinra group and also higher in patients receiving anakinra compared to SoC. Our study indicates that intravenous high dose anakinra treatment is safe and effective in patients with COVID-19 associated cytokine storm accompanying cancer.
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