Evidence map›Paper›PMID 39652286›Full record

ArticleInfectious diseases and therapy2025

Preventing Severe COVID-19 with Tixagevimab-Cilgavimab in Hematological Patients Treated with Anti-CD20 Monoclonal Antibodies: An International Multicenter Study.

Hovav Azuly, Tali Shafat, Daniel Grupel, Tzvika Porges, Ran Abuhasira, Ana Belkin, Ofir Deri, Yonatan Oster, Shadi Zahran, Ehud Horwitz and 19 more

Abstract read
In one paragraph

Article in Infectious diseases and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

29 authors.

Hovav Azuly *Infectious Diseases Institute, Soroka University Medical Center, and the Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Tali Shafat *Infectious Diseases Institute, Soroka University Medical Center, and the Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Daniel GrupelDepartment of Clinical Microbiology and Infectious Diseases, Hadassah Medical Center, Jerusalem, Israel.
Tzvika PorgesHematology Department, Soroka University Medical Center, Beer-Sheva, Israel.
Ran AbuhasiraClinical Research Center, Soroka University Medical Center and the Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Ana BelkinInternal Medicine D and Infectious Diseases Unit, Sheba Medical Center, Ramat-Gan, Israel.
Ofir DeriInternal Medicine T, Sheba Medical Center, Ramat-Gan, Israel.
Yonatan OsterDepartment of Clinical Microbiology and Infectious Diseases, Hadassah Medical Center, Jerusalem, Israel.
Shadi ZahranDepartment of Clinical Microbiology and Infectious Diseases, Hadassah Medical Center, Jerusalem, Israel.
Ehud HorwitzDepartment of Clinical Microbiology and Infectious Diseases, Hadassah Medical Center, Jerusalem, Israel.
Netanel A HorowitzDepartment of Hematology and Bone Marrow Transplantation, Rambam Health Care Campus, Haifa, Israel.
Hazim KhatibDepartment of Hematology and Bone Marrow Transplantation, Rambam Health Care Campus, Haifa, Israel.
Marjorie Vieira BatistaDepartment of Infectious Diseases, AC Camargo Cancer Center, São Paulo, SP, Brazil.
Anita Cassoli CortezDepartment of Hematology and Cell Therapy, AC Camargo Cancer Center, São Paulo, SP, Brazil.
Tal Brosh-NissimovInfectious Diseases Unit, Samson Assuta Ashdod University Hospital, Ashdod, Israel.
Yafit SegmanHematology Institute, Samson Assuta Ashdod University Hospital, Ashdod, Israel.
Linor IshayRappaport Faculty of Medicine, Technion-Israel Institute of Technology, 3109601, Haifa, Israel.
Regev CohenRappaport Faculty of Medicine, Technion-Israel Institute of Technology, 3109601, Haifa, Israel.
Alaa AtamnaInfectious Diseases Unit, Rabin Medical Center, Beilinson Hospital, Petah Tikva, Israel.
Amy SpalloneDepartment of Infectious Diseases, Infection Control and Employee Health, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Roy F ChemalyDepartment of Infectious Diseases, Infection Control and Employee Health, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Juan Carlos RamosInfectious Disease Unit, Internal Medicine Service, CIBERINFEC. Hospital Universitario La Paz, Madrid, Spain.
Michal ChowersMeir Medical Centre, Kfar Saba, Israel.
Evgeny RogozinInfectious Diseases Unit, Shamir (Assaf Harofeh) Medical Center, Be'er Ya'akov, Israel.
Noga Carmi OrenInfectious Diseases Unit, Shamir (Assaf Harofeh) Medical Center, Be'er Ya'akov, Israel.
Şiran KeskeDepartment of Infectious Diseases, VKV American Hospital, Koç University İşbank Center for Infectious Diseases (KUISCID), Istanbul, Turkey.
Orit Wolfovitz BarchadInfectious Disease Unit, Shaare Zedek Medical Center, Jerusalem, Israel.
Lior NesherInfectious Diseases Institute, Soroka University Medical Center, and the Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel. nesherke@bgu.ac.il.ORCID http://orcid.org/0000-0002-1230-0428
European Society of Clinical Microbiology and Infectious Diseases (ESCMID) Study Group for Respiratory Viruses (ESGREV)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDespite the declining public health emergency status, COVID-19 still poses significant risks, especially for immunocompromised individuals. We aimed to evaluate the effectiveness of tixagevimab-cilgavimab (T-C) prophylaxis in preventing severe COVID-19 in patients with hematologic malignancies (HM) treated with anti-CD20 therapy during the early Omicron variant phase of the pandemic.

methodsThe European Society of Clinical Microbiology and Infectious Diseases Study Group for Respiratory Viruses (ESGREV) conducted a multicenter retrospective cohort study involving 15 centers from 5 countries. The study included 749 patients with HM treated with anti-CD20 between February 15 and June 30, 2022, comparing 215 who received T-C prophylaxis to 534 who did not.

resultsThe study revealed a significant reduction in the risk of COVID-19 among patients who received T-C prophylaxis compared to those who did not (11.2% vs 23.4%, p < 0.001), with hazard ratio (HR) of 0.40 (95% CI 0.26-0.63), adjusted for age, sex, vaccination status, baseline HM malignancy and type of anti-CD-20. We also demonstrated a reduction for severe-critical diseases within all study populations, 1.4% vs 5.2%, p = 0.017, HR 0.26 (95% CI 0.08-0.84).

conclusionT-C prophylaxis effectively prevented COVID-19 and severe-critical COVID-19 in patients with HM treated with anti-CD20 monoclonal antibodies during the early Omicron variant phase of the pandemic. Even though T-C is ineffective against current variants, these findings highlight the importance of additional protective measures and the continued development of monoclonal antibodies to protect immunocompromised individuals to mitigate the impact of COVID-19 and other respiratory viral diseases.

Indexed as

Anti-CD20COVID-19Hematologic malignanciesMonoclonal antibodiesTixagevimab-cilgavimab

Identifiers

PMID39652286
PMCPMC11782782

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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 OpenQuestion graph.