Evidence map›Paper›PMID 41776490›Full record

ArticleBMC cancer2026

Azvudine for the treatment of cancer patients with COVID-19: a multicenter, real-world, retrospective, cohort study.

Lei Li, Wenjie Liu, Ling Wang, Mengzhao Yang, Juan Wang, Guotao Li, Guowu Qian, Shixi Zhang, Donghai Liu, Hong Luo and 4 more

Abstract readMulticenter Study
In one paragraph

Article in BMC cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Lei Li *Department of Infectious Diseases, State Key Laboratory of Antiviral Drugs, Pingyuan Laboratory, the First Affiliated Hospital of Zhengzhou University, #1 Jianshe East Road, Zhengzhou, 450052, China.
Wenjie Liu *Pain Department of the First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China.
Ling WangDepartment of Clinical Laboratory, Henan Provincial Chest Hospital Affiliated of Zhengzhou University, Zhengzhou, 450008, China.
Mengzhao YangDepartment of Infectious Diseases, State Key Laboratory of Antiviral Drugs, Pingyuan Laboratory, the First Affiliated Hospital of Zhengzhou University, #1 Jianshe East Road, Zhengzhou, 450052, China.
Juan WangDepartment of Liver Disease, the Affiliated Infectious Disease Hospital of Zhengzhou University, Zhengzhou, 450052, China.
Guotao LiDepartment of Infectious Diseases, Luoyang Central Hospital Affiliated of Zhengzhou University, Luoyang, 471000, China.
Guowu QianDepartment of Gastrointestinal Surgery, Nanyang Central Hospital, Nanyang, 473009, China.
Shixi ZhangDepartment of Infectious Diseases, Shangqiu Municipal Hospital, Shangqiu, 476000, China.
Donghai LiuDepartment of Clinical Laboratory, Henan Provincial Chest Hospital Affiliated of Zhengzhou University, Zhengzhou, 450008, China.
Hong LuoGuangshan County People's Hospital, Guangshan County, Xinyang, 465450, China.
Silin LiDepartment of Respiratory and Critical Care Medicine, Fengqiu County People's Hospital, Xinxiang, 453300, China.
Donghua ZhangDepartment of Infectious Diseases, Anyang City Fifth People's Hospital, Anyang, 455000, China.
Zujiang YuDepartment of Infectious Diseases, State Key Laboratory of Antiviral Drugs, Pingyuan Laboratory, the First Affiliated Hospital of Zhengzhou University, #1 Jianshe East Road, Zhengzhou, 450052, China. johnyuem@zzu.edu.cn.
Zhigang RenDepartment of Infectious Diseases, State Key Laboratory of Antiviral Drugs, Pingyuan Laboratory, the First Affiliated Hospital of Zhengzhou University, #1 Jianshe East Road, Zhengzhou, 450052, China. fccrenzg@zzu.edu.cn.

Funding

National Key Research and Development Program of China 2022YFC2303100National Key Research and Development Program of China 2023YFC3043514Scientific and Technological Innovation Talents of Universities in Henan Province 24HASTIT063Scientific Research and Innovation Team of The First Affiliated Hospital of Zhengzhou University QNCXTD2023002Scientific Research and Innovation Team of The First Affiliated Hospital of Zhengzhou University ZYCXTD2023002Young and Middle-aged Academic Leaders of Henan Provincial Health Commission HNSWJW-2022013
6 · The paper itself

Abstract

backgroundCancer patients are at an elevated risk for SARS-CoV-2 infection and require vigilant monitoring. The efficacy and safety of Azvudine in treating COVID-19 among this vulnerable group remain under-researched.

methodsWe conducted a multicenter, retrospective cohort study of nine hospitals involving cancer patients with COVID-19 hospitalized from December 2022 to January 2023. To minimize immortal time bias, patients who died or were discharged within 24 h of drug administration were excluded. A 2:1 propensity score matching (PSM) was performed to balance baseline characteristics, explicitly adjusting for tumor metastasis, tumor classification, and COVID-19 vaccination status. The primary outcome was 30-day all-cause death, and the secondary outcome was composite disease progression. Robustness was verified using Probit regression and double robust estimation with Augmented Inverse Probability Weighting (AIPW).

resultsA total of 1,829 patients were included in the final matched cohort (1,200 in the control group and 629 in the Azvudine group). Azvudine treatment was significantly associated with a reduced risk of all-cause death (adjusted hazard ratio [HR]: 0.65, 95% CI: 0.452–0.939, P = 0.022). Furthermore, unlike unadjusted analyses, the multivariate model demonstrated a significant reduction in composite disease progression (adjusted HR: 0.70, 95% CI: 0.518–0.936, P = 0.016). These findings were consistent across all sensitivity analyses. Regarding safety, the Azvudine group exhibited a higher incidence of hypokalemia (P < 0.001) and Grade ≥3b platelet count decreased (P = 0.002). Significant fluctuations in lymphocyte counts (increased rates of both decrease and increase) were also observed.

conclusionAzvudine significantly reduced the risk of all-cause mortality and disease progression in hospitalized cancer patients with COVID-19. Although the drug was associated with increased risks of specific laboratory abnormalities (hypokalemia and thrombocytopenia), the substantial survival benefit outweighs these manageable risks. Routine clinical monitoring of electrolytes and blood counts is recommended during treatment.

Indexed as

Antiviral AgentsCOVID-19COVID-19 Drug TreatmentNeoplasmsAgedDisease ProgressionFemaleHumansMaleMiddle AgedRetrospective StudiesSARS-CoV-2Antiviral AgentsAll-cause deathAzvudineCancer patientsComposite disease progressionCOVID-19

Identifiers

PMID41776490
PMCPMC13067604

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.