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雄激素剥夺疗法对前列腺癌男性 COVID-19 疾病的影响。

The Impact of Androgen Deprivation Therapy on COVID-19 Illness in Men With Prostate Cancer.

机构信息

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Department of Medicine, Weill Cornell Medical Center, New York, NY, USA.

出版信息

JNCI Cancer Spectr. 2022 May 2;6(3). doi: 10.1093/jncics/pkac035.

Abstract

BACKGROUND

TMPRSS2, a cell surface protease regulated by androgens and commonly upregulated in prostate cancer (PCa), is a necessary component for SARS-CoV-2 viral entry into respiratory epithelial cells. Previous reports suggested a lower risk of SARS-CoV-2 among PCa patients on androgen deprivation therapy (ADT). However, the impact of ADT on severe COVID-19 illness is poorly understood.

METHODS

We performed a multicenter study across 7 US medical centers and evaluated patients with PCa and SARS-CoV-2 detected by polymerase-chain-reaction between March 1, 2020, and May 31, 2020. PCa patients were considered on ADT if they had received appropriate ADT treatment within 6 months of COVID-19 diagnosis. We used multivariable logistic and Cox proportional-hazard regression models for analysis. All statistical tests were 2-sided.

RESULTS

We identified 465 PCa patients (median age = 71 years) with a median follow-up of 60 days. Age, body mass index, cardiovascular comorbidity, and PCa clinical disease state adjusted overall survival (hazard ratio [HR] = 1.16, 95% confidence interval [CI] = 0.68 to 1.98, P = .59), hospitalization status (HR = 0.96, 95% CI = 0.52 to 1.77, P = .90), supplemental oxygenation (HR 1.14, 95% CI = 0.66 to 1.99, P = .64), and use of mechanical ventilation (HR = 0.81, 95% CI = 0.25 to 2.66, P = .73) were similar between ADT and non-ADT cohorts. Similarly, the addition of androgen receptor-directed therapy within 30 days of COVID-19 diagnosis to ADT vs ADT alone did not statistically significantly affect overall survival (androgen receptor-directed therapy: HR = 1.27, 95% CI = 0.69 to 2.32, P = .44).

CONCLUSIONS

In this retrospective cohort of PCa patients, the use of ADT was not demonstrated to influence severe COVID-19 outcomes, as defined by hospitalization, supplemental oxygen use, or death. Age 70 years and older was statistically significantly associated with a higher risk of developing severe COVID-19 disease.

摘要

背景

TMPRSS2 是一种受雄激素调节并在前列腺癌(PCa)中普遍上调的细胞表面蛋白酶,是 SARS-CoV-2 病毒进入呼吸道上皮细胞的必要组成部分。先前的报告表明,接受雄激素剥夺疗法(ADT)的 PCa 患者感染 SARS-CoV-2 的风险较低。然而,ADT 对严重 COVID-19 疾病的影响尚不清楚。

方法

我们在 7 家美国医疗中心进行了一项多中心研究,并评估了 2020 年 3 月 1 日至 2020 年 5 月 31 日期间通过聚合酶链反应检测到的患有 PCa 和 SARS-CoV-2 的患者。如果 PCa 患者在 COVID-19 诊断后 6 个月内接受了适当的 ADT 治疗,则认为他们正在接受 ADT。我们使用多变量逻辑和 Cox 比例风险回归模型进行分析。所有统计检验均为双侧。

结果

我们确定了 465 名 PCa 患者(中位年龄为 71 岁),中位随访时间为 60 天。年龄、体重指数、心血管合并症和 PCa 临床疾病状态调整后的总体生存率(风险比 [HR] = 1.16,95%置信区间 [CI] = 0.68 至 1.98,P = 0.59)、住院状态(HR = 0.96,95%CI = 0.52 至 1.77,P = 0.90)、补充氧气(HR 1.14,95%CI = 0.66 至 1.99,P = 0.64)和机械通气的使用(HR = 0.81,95%CI = 0.25 至 2.66,P = 0.73)在 ADT 和非 ADT 队列之间相似。同样,在 COVID-19 诊断后 30 天内添加雄激素受体靶向治疗与 ADT 相比并未显着影响总体生存率(雄激素受体靶向治疗:HR = 1.27,95%CI = 0.69 至 2.32,P = 0.44)。

结论

在这项针对 PCa 患者的回顾性队列研究中,没有发现 ADT 的使用会影响住院、使用补充氧气或死亡等定义的严重 COVID-19 结局。70 岁及以上的年龄与发生严重 COVID-19 疾病的风险增加呈统计学显著相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3faf/9165550/77239e65143b/pkac035f1.jpg

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