Evidence map›Paper›PMID 39711119›Full record

ArticleCancer medicine2024

One Year Duration of Immune Response Following a 3rd Booster Dose of mRNA Vaccine Against COVID-19 in 292 Patients With Hematological Malignancies in University Hospital Ostrava, Czech Republic.

Ondrej Šušol, Barbora Šušolová, Ondřej Klempíř, Milan Navrátil, Jaromír Gumulec, Zdeněk Kořístek, Juraj Ďuraš, Michal Kaščák, Jana Mihályová, Lukáš Stejskal and 14 more

Abstract read
In one paragraph

Article in Cancer medicine, 2024. 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. Trial
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

24 authors.

Ondrej ŠušolDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.ORCID 0000-0001-7820-5987
Barbora ŠušolováDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Ondřej KlempířDepartment of Biomedical Informatics, Faculty of Biomedical Engineering, Czech Technical University in Prague, Prague, Czech Republic.
Milan NavrátilDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Jaromír GumulecDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Zdeněk KořístekDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Juraj ĎurašDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Michal KaščákDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Jana MihályováDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Lukáš StejskalDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Tomáš JelínekDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Petra RichterováDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Lenka SzeligováDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Hana PlonkováDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Jana ZuchnickáDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Barbora DluhošováDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Ivo DemelDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.ORCID 0000-0002-0518-9581
David BuffaDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Katarína HradskáDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Tereza PopkováDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.ORCID 0000-0001-5885-4218
Ludmila MuroňováDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.ORCID 0009-0003-8589-1577
Martin LachnitDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Klára LančováDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.
Roman HájekDepartment of Haemato-Oncology, University Hospital Ostrava, Ostrava, Czech Republic.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsTo evaluate antibody response to mRNA vaccine, identify subgroups with poor response and to determine long-term antibody durability in hematological patients. MATERIALS AND

methodsWe have vaccinated 292 patients with all hematological malignancies with a third dose of mRNA COMIRNATY vaccine with a 12-month follow-up period in our center in Ostrava, Czech Republic.

resultsAntibody response for the whole cohort exceeded 74% through the whole 12-month follow-up. Lowest seroconversion was observed in CLL cohort (20/41, 48.8%), patients who received anti-CD20 therapy < 6 months before vaccination (8/30, 26.7%) and BTK inhibitors (3/6, 50.0%). On the contrary, patients with chronic myeloproliferative neoplasms and acute leukemia performed comparably with healthy population (33/33; 100% and 12/13; 92.3%, respectively). We have seen better results if the time interval between anti-CD20 therapy and additional vaccine dose was longer than 6 months (5/8 patients achieved seroconversion on 4th booster dose after previous failure). Also, 36 patients received a 4th dose of vaccine as a booster with measurable increase in protective antibodies in 50% (18/36).

conclusionsAdditional doses show promise for a well-timed revaccination even in poor responders. To our knowledge, no study comparable to our work in terms of follow-up length, vaccine consistency or variety of hematological malignancies and/or treatment has been reported yet. Our findings shed more light on long-term antibody response to mRNA vaccines against SARS-CoV-2 in patients with hematological cancer and bring important data for the evaluation of possible vaccine failure and scheduling of subsequent doses.

Indexed as

Antibodies, ViralCOVID-19COVID-19 VaccinesHematologic NeoplasmsImmunization, SecondarySARS-CoV-2AdultAgedAged, 80 and overCzech RepublicFemaleFollow-Up StudiesHumansMaleMiddle AgedmRNA VaccinesAntibodies, ViralCOVID-19 VaccinesmRNA VaccinesCancerCOVID‐19LeukemiaLymphomaMyelomaVaccination

Identifiers

PMID39711119
PMCPMC11664122

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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.