tetano
Editor, Senior Moderator
EClinicalMedicine
. 2024 Feb 9:69:102468.
doi: 10.1016/j.eclinm.2024.102468. eCollection 2024 Mar. Antiviral effectiveness and survival correlation of azvudine and nirmatrelvir/ritonavir in elderly severe patients with COVID-19: a retrospective real-world study
Shuxia Wang[SUP] 1 [/SUP], Jin Sun[SUP] 1 2 [/SUP], Xin Zhang[SUP] 3 [/SUP], Man Li[SUP] 1 [/SUP], Bangguo Qin[SUP] 2 [/SUP], Miao Liu[SUP] 4 [/SUP], Nan Zhang[SUP] 2 [/SUP], Shengshu Wang[SUP] 5 [/SUP], Tingyu Zhou[SUP] 6 [/SUP], Wei Zhang[SUP] 7 [/SUP], Cong Ma[SUP] 8 [/SUP], Xinli Deng[SUP] 9 [/SUP], Yongyi Bai[SUP] 10 [/SUP], Geping Qu[SUP] 11 [/SUP], Lin Liu[SUP] 11 [/SUP], Hui Shi[SUP] 12 [/SUP], Bo Zhou[SUP] 13 [/SUP], Ke Li[SUP] 13 [/SUP], Bo Yang[SUP] 14 [/SUP], Suxia Li[SUP] 14 [/SUP], Fan Wang[SUP] 10 [/SUP], Jinling Ma[SUP] 10 [/SUP], Lu Zhang[SUP] 10 [/SUP], Yajuan Wang[SUP] 11 [/SUP], Li An[SUP] 11 [/SUP], Wenhui Liu[SUP] 12 [/SUP], Qing Chang[SUP] 12 [/SUP], Ru Zhang[SUP] 12 [/SUP], Xi Yin[SUP] 13 [/SUP], Yang Yang[SUP] 13 [/SUP], Qiangguo Ao[SUP] 15 [/SUP], Qiang Ma[SUP] 15 [/SUP], Shuangtong Yan[SUP] 16 [/SUP], Haili Huang[SUP] 17 [/SUP], Peng Song[SUP] 17 [/SUP], Linggen Gao[SUP] 18 [/SUP], Wenning Lu[SUP] 18 [/SUP], Lining Xu[SUP] 18 [/SUP], Li Lei[SUP] 8 [/SUP], Keyu Wang[SUP] 9 [/SUP], Qi Zhang[SUP] 3 [/SUP], Qing Song[SUP] 19 [/SUP], Zhijian Zhang[SUP] 11 [/SUP], Xiangqun Fang[SUP] 11 [/SUP], Yao He[SUP] 5 [/SUP], Tianzhi Li[SUP] 3 [/SUP], Ping Zhu[SUP] 1 [/SUP]
Affiliations
Background: Azvudine and nirmatrelvir/ritonavir are approved to treat mild-to-moderate coronavirus disease 2019 (COVID-19) in adults with a high risk for progression to severe infection. We sought to compare the antiviral effectiveness and clinical outcomes of elderly severe patients with COVID-19 receiving these two antiviral agents.
Methods: In this observational study, we identified 249 elderly patients with severe COVID-19 infection who were admitted to the Second Medical Center of the People's Liberation Army General Hospital from December 2022 to January 2023, including 128 azvudine recipients, 66 nirmatrelvir/ritonavir recipients and 55 patients not received antiviral treatments. We compared the cycle threshold (Ct) value dynamic change of all three groups. The primary outcome was a composite outcome of disease progression, including all-cause death, intensive care unit admission, and initiation of invasive mechanical ventilation. The outcomes of all enrolled patients were followed up from the electronic medical record system. Kaplan-Meier and Cox risk proportional regression analyses were used to compare the clinical outcomes of all three groups. To more directly compare the effectiveness of the two antiviral drugs, we performed propensity-score matching between the two antiviral groups and compared antiviral efficacy and clinical outcomes in the matched population.
Findings: Among 249 patients (mean age, 91.41 years), 77 patients died during the follow-up period. When compared to patients who did not receive any antivirals, neither nirmatrelvir/ritonavir nor azvudine demonstrated a survival benefit. The Cox analysis of the all-cause death of the three groups showed that the risk of death was 0.730 (0.423-1.262) in the azvudine group 0.802 (0.435-1.480) and in the nirmatrelvir/ritonavir group compared with the non-antiviral group. After propensity score matching, we included 58 azvudine recipients and 58 nirmatrelvir/ritonavir recipients. The fitted curve of the Ct value after matching illustrated that the rate of viral decline in the early stage of nirmatrelvir/ritonavir treatment seems to surpass that of azvudine, but there was no statistical significance. Azvudine was seemly associated with a lower risk of composite outcomes (HR:1.676, 95% CI:0.805-3.488) and short-term all-cause death (HR: 1.291, 95%CI: 0.546-3.051).
Interpretation: Patients who received azvudine have a similar antiviral effectiveness and survival curve trend compared to nirmatrelvir/ritonavir. In this limited series, antiviral treatment was not associated with a significant clinical benefit. This lack of clinical benefit might be attributed to potential bias.
Funding: This study was supported by the "National Key R&D Program of China" (Funding No. 2020YFC2008900) and the National Defense Science and Technology Innovation Special Zone Project (223-CXCY-N101-07-18-01).
Keywords: Azvudine; COVID-19; Elderly; Nirmatrelvir/ritonavir.
. 2024 Feb 9:69:102468.
doi: 10.1016/j.eclinm.2024.102468. eCollection 2024 Mar. Antiviral effectiveness and survival correlation of azvudine and nirmatrelvir/ritonavir in elderly severe patients with COVID-19: a retrospective real-world study
Shuxia Wang[SUP] 1 [/SUP], Jin Sun[SUP] 1 2 [/SUP], Xin Zhang[SUP] 3 [/SUP], Man Li[SUP] 1 [/SUP], Bangguo Qin[SUP] 2 [/SUP], Miao Liu[SUP] 4 [/SUP], Nan Zhang[SUP] 2 [/SUP], Shengshu Wang[SUP] 5 [/SUP], Tingyu Zhou[SUP] 6 [/SUP], Wei Zhang[SUP] 7 [/SUP], Cong Ma[SUP] 8 [/SUP], Xinli Deng[SUP] 9 [/SUP], Yongyi Bai[SUP] 10 [/SUP], Geping Qu[SUP] 11 [/SUP], Lin Liu[SUP] 11 [/SUP], Hui Shi[SUP] 12 [/SUP], Bo Zhou[SUP] 13 [/SUP], Ke Li[SUP] 13 [/SUP], Bo Yang[SUP] 14 [/SUP], Suxia Li[SUP] 14 [/SUP], Fan Wang[SUP] 10 [/SUP], Jinling Ma[SUP] 10 [/SUP], Lu Zhang[SUP] 10 [/SUP], Yajuan Wang[SUP] 11 [/SUP], Li An[SUP] 11 [/SUP], Wenhui Liu[SUP] 12 [/SUP], Qing Chang[SUP] 12 [/SUP], Ru Zhang[SUP] 12 [/SUP], Xi Yin[SUP] 13 [/SUP], Yang Yang[SUP] 13 [/SUP], Qiangguo Ao[SUP] 15 [/SUP], Qiang Ma[SUP] 15 [/SUP], Shuangtong Yan[SUP] 16 [/SUP], Haili Huang[SUP] 17 [/SUP], Peng Song[SUP] 17 [/SUP], Linggen Gao[SUP] 18 [/SUP], Wenning Lu[SUP] 18 [/SUP], Lining Xu[SUP] 18 [/SUP], Li Lei[SUP] 8 [/SUP], Keyu Wang[SUP] 9 [/SUP], Qi Zhang[SUP] 3 [/SUP], Qing Song[SUP] 19 [/SUP], Zhijian Zhang[SUP] 11 [/SUP], Xiangqun Fang[SUP] 11 [/SUP], Yao He[SUP] 5 [/SUP], Tianzhi Li[SUP] 3 [/SUP], Ping Zhu[SUP] 1 [/SUP]
Affiliations
- PMID: 38361990
- PMCID: PMC10867603
- DOI: 10.1016/j.eclinm.2024.102468
Background: Azvudine and nirmatrelvir/ritonavir are approved to treat mild-to-moderate coronavirus disease 2019 (COVID-19) in adults with a high risk for progression to severe infection. We sought to compare the antiviral effectiveness and clinical outcomes of elderly severe patients with COVID-19 receiving these two antiviral agents.
Methods: In this observational study, we identified 249 elderly patients with severe COVID-19 infection who were admitted to the Second Medical Center of the People's Liberation Army General Hospital from December 2022 to January 2023, including 128 azvudine recipients, 66 nirmatrelvir/ritonavir recipients and 55 patients not received antiviral treatments. We compared the cycle threshold (Ct) value dynamic change of all three groups. The primary outcome was a composite outcome of disease progression, including all-cause death, intensive care unit admission, and initiation of invasive mechanical ventilation. The outcomes of all enrolled patients were followed up from the electronic medical record system. Kaplan-Meier and Cox risk proportional regression analyses were used to compare the clinical outcomes of all three groups. To more directly compare the effectiveness of the two antiviral drugs, we performed propensity-score matching between the two antiviral groups and compared antiviral efficacy and clinical outcomes in the matched population.
Findings: Among 249 patients (mean age, 91.41 years), 77 patients died during the follow-up period. When compared to patients who did not receive any antivirals, neither nirmatrelvir/ritonavir nor azvudine demonstrated a survival benefit. The Cox analysis of the all-cause death of the three groups showed that the risk of death was 0.730 (0.423-1.262) in the azvudine group 0.802 (0.435-1.480) and in the nirmatrelvir/ritonavir group compared with the non-antiviral group. After propensity score matching, we included 58 azvudine recipients and 58 nirmatrelvir/ritonavir recipients. The fitted curve of the Ct value after matching illustrated that the rate of viral decline in the early stage of nirmatrelvir/ritonavir treatment seems to surpass that of azvudine, but there was no statistical significance. Azvudine was seemly associated with a lower risk of composite outcomes (HR:1.676, 95% CI:0.805-3.488) and short-term all-cause death (HR: 1.291, 95%CI: 0.546-3.051).
Interpretation: Patients who received azvudine have a similar antiviral effectiveness and survival curve trend compared to nirmatrelvir/ritonavir. In this limited series, antiviral treatment was not associated with a significant clinical benefit. This lack of clinical benefit might be attributed to potential bias.
Funding: This study was supported by the "National Key R&D Program of China" (Funding No. 2020YFC2008900) and the National Defense Science and Technology Innovation Special Zone Project (223-CXCY-N101-07-18-01).
Keywords: Azvudine; COVID-19; Elderly; Nirmatrelvir/ritonavir.