Department of Infectious Diseases, Infection Control and Employee Health, The University of Texas MD Anderson Cancer Center, Houston, United States.
Division of Infectious Diseases, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, United States.
Elife. 2023 Jan 30;12:e81127. doi: 10.7554/eLife.81127.
In this international multicenter study, we aimed to determine the independent risk factors associated with increased 30 day mortality and the impact of cancer and novel treatment modalities in a large group of patients with and without cancer with COVID-19 from multiple countries.
We retrospectively collected de-identified data on a cohort of patients with and without cancer diagnosed with COVID-19 between January and November 2020 from 16 international centers.
We analyzed 3966 COVID-19 confirmed patients, 1115 with cancer and 2851 without cancer patients. Patients with cancer were more likely to be pancytopenic and have a smoking history, pulmonary disorders, hypertension, diabetes mellitus, and corticosteroid use in the preceding 2 wk (p≤0.01). In addition, they were more likely to present with higher inflammatory biomarkers (D-dimer, ferritin, and procalcitonin) but were less likely to present with clinical symptoms (p≤0.01). By country-adjusted multivariable logistic regression analyses, cancer was not found to be an independent risk factor for 30 day mortality (p=0.18), whereas lymphopenia was independently associated with increased mortality in all patients and in patients with cancer. Older age (≥65y) was the strongest predictor of 30 day mortality in all patients (OR = 4.47, p<0.0001). Remdesivir was the only therapeutic agent independently associated with decreased 30 day mortality (OR = 0.64, p=0.036). Among patients on low-flow oxygen at admission, patients who received remdesivir had a lower 30 day mortality rate than those who did not (5.9 vs 17.6%; p=0.03).
Increased 30 day all-cause mortality from COVID-19 was not independently associated with cancer but was independently associated with lymphopenia often observed in hematolgic malignancy. Remdesivir, particularly in patients with cancer receiving low-flow oxygen, can reduce 30 day all-cause mortality.
National Cancer Institute and National Institutes of Health.
在这项国际多中心研究中,我们旨在确定与 COVID-19 患者 30 天死亡率增加相关的独立危险因素,以及癌症和新型治疗方式的影响,这些患者来自多个国家,既有癌症也有无癌症。
我们回顾性地收集了 2020 年 1 月至 11 月期间来自 16 个国际中心的确诊 COVID-19 患者(有癌症和无癌症)的匿名数据。
我们分析了 3966 例 COVID-19 确诊患者,其中 1115 例有癌症,2851 例无癌症。与无癌症患者相比,癌症患者更有可能出现全血细胞减少、有吸烟史、肺部疾病、高血压、糖尿病和 2 周内使用皮质类固醇(p≤0.01)。此外,他们更有可能出现更高的炎症生物标志物(D-二聚体、铁蛋白和降钙素原),但出现临床症状的可能性较小(p≤0.01)。通过国家调整的多变量逻辑回归分析,癌症并不是 30 天死亡率的独立危险因素(p=0.18),而淋巴细胞减少在所有患者和癌症患者中均与死亡率增加独立相关。所有患者中,年龄≥65 岁(OR=4.47,p<0.0001)是 30 天死亡率的最强预测因子。瑞德西韦是唯一与降低 30 天死亡率独立相关的治疗药物(OR=0.64,p=0.036)。在入院时接受低流量吸氧的患者中,接受瑞德西韦治疗的患者 30 天死亡率低于未接受瑞德西韦治疗的患者(5.9% vs 17.6%;p=0.03)。
COVID-19 患者 30 天全因死亡率的增加与癌症无关,但与血液恶性肿瘤中常见的淋巴细胞减少独立相关。瑞德西韦,特别是在接受低流量氧气的癌症患者中,可以降低 30 天全因死亡率。
美国国立癌症研究所和美国国立卫生研究院。