Evidence map›Paper›PMID 34453830›Full record

ArticleJournal of the National Cancer Institute2022

Immunogenicity and Safety of the BNT162b2 mRNA COVID-19 Vaccine Among Actively Treated Cancer Patients.

Hagai Ligumsky, Esraa Safadi, Tal Etan, Noam Vaknin, Manuel Waller, Assaf Croll, Alla Nikolaevski-Berlin, Inbal Greenberg, Tami Halperin, Asaf Wasserman and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 9 pooled it
4.9field-weighted citation impact, top 4% of its field
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

56 citing papers in PubMed, 9 syntheses or guidelines pooled it, 82 citations in OpenAlex.

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  9. Immunological and clinical efficacy of COVID-19 vaccines in immunocompromised populations: a systematic review.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Hagai LigumskyOncology Division, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.ORCID 0000-0002-5652-3703
Esraa SafadiSackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Tal EtanOncology Division, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Noam VakninSackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.ORCID 0000-0003-3827-6814
Manuel WallerOncology Division, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Assaf CrollSackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Alla Nikolaevski-BerlinOncology Division, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Inbal GreenbergOncology Division, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.ORCID 0000-0003-3972-7146
Tami HalperinHuman Immunodeficiency Virus Lab, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Asaf WassermanOncology Division, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Lior GalazanThe Integrated Cancer Prevention Center, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Nadir ArberThe Integrated Cancer Prevention Center, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Ido WolfOncology Division, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Tel Aviv University · ILTel Aviv Sourasky Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundActivity and safety of the SARS-CoV-2 BNT162b2 vaccine in actively treated patients with solid tumors is currently unknown.

methodsWe conducted a retrospective study of 326 patients with solid tumors treated with anticancer medications to determine the proportion of cancer patients with immunogenicity against SARS-CoV-2 following 2 doses of the BNT162b2 vaccine. The control group comprised 164 vaccinated healthy adults. Anti-SARS-CoV-2 S immunoglobulin G antibodies were measured using a level greater than 50 AU/mL as a cutoff for seropositivity. Information on adverse effects was collected using a questionnaire. All statistical tests were 2-sided.

resultsMost patients (205, 62.9%) were treated with chemotherapy either alone or with additional therapy; 55 (16.9%) were treated with immune checkpoint inhibitors and 38 (11.7%) with targeted therapy alone; 28 (8.6%) received other combinations. The vaccine was well tolerated, and no severe side effects were reported. Among patients with cancer, 39 (11.9%) were seronegative compared with 5 (3.0%) of the control group (P = .001). Median immunoglobulin G titers were statistically significantly lower among patients with cancer compared with control (931 AU/mL vs 2817 AU/mL, P = .003). Seronegativity proportions were higher in the chemotherapy-treated group (n = 19; 18.8%) compared with the immune checkpoint inhibitor-treated patients (n = 5; 9.1%) and with those treated with targeted therapy (n = 1; 2.6%) (P = .02). Titers were also statistically significantly different among treatment types (P = .002).

conclusionsThe BNT162b2 vaccine is safe and effective in actively treated patients with cancer. The relatively lower antibody titers and lower proportion of seropositive patients, especially among chemotherapy-treated patients, call for continuing the use of personal protective measures in these patients, even following vaccination.

Indexed as

COVID-19NeoplasmsAdultAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesHumansImmunogenicity, VaccineProspective StudiesRetrospective StudiesRNA, MessengerSARS-CoV-2Antibodies, ViralBNT162 VaccineCOVID-19 VaccinesRNA, Messenger

Identifiers

PMID34453830
PMCPMC8499747
OpenAlexW3197493891

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.