Evidence map›Paper›PMID 36530752›Full record

ArticleClinical infection in practice2023

Third dose of an mRNA COVID-19 vaccine for patients with multiple myeloma.

Marissa-Skye Goldwater, Samuel D Stampfer, Bernard Sean Regidor, Sean Bujarski, Scott Jew, Haiming Chen, Ning Xu, Clara Kim, Susanna Kim, James R Berenson

Open access · goldAbstract read
In one paragraph

Article in Clinical infection in practice, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Marissa-Skye GoldwaterInstitute for Myeloma and Bone Cancer Research, West Hollywood, CA, United States.
Samuel D StampferDivision of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, GA, United States.
Bernard Sean RegidorBerenson Cancer Center, West Hollywood, CA, United States.
Sean BujarskiInstitute for Myeloma and Bone Cancer Research, West Hollywood, CA, United States.
Scott JewInstitute for Myeloma and Bone Cancer Research, West Hollywood, CA, United States.
Haiming ChenInstitute for Myeloma and Bone Cancer Research, West Hollywood, CA, United States.
Ning XuInstitute for Myeloma and Bone Cancer Research, West Hollywood, CA, United States.
Clara KimONCOtherapeutics, West Hollywood, CA, United States.
Susanna KimONCOtherapeutics, West Hollywood, CA, United States.
James R BerensonInstitute for Myeloma and Bone Cancer Research, West Hollywood, CA, United States.
Institute for Myeloma & Bone Cancer Research · USOncotherapeutics (United States) · USEmory University · US

Funding

Training a New Generation of VaccinologistsT32AI074492 · NIAID · EMORY UNIVERSITY · PI Rama Rao Amara, Benjamin A Lopman · 2009 to 2026
$6.4M
NIAID NIH HHS T32 AI074492
6 · The paper itself

Abstract

We have reported that IgG antibody responses following two mRNA COVID-19 vaccinations are impaired among patients with multiple myeloma (MM). In the current study, sixty-seven patients with MM were tested for anti-spike IgG antibodies 0-60 days prior to their first vaccination, 14-28 days following the second dose, and both before and 14-28 days after their third dose of the mRNA-1273 or BNT162b2 vaccines. After the first two doses, most patients' (93 %) antibody levels declined to ineffective levels (<250 BAU/mL) prior to their third dose (D3). D3 elicited responses in 84 % of patients (61 % full response and 22 % partial response). The third vaccination increased antibody levels (average = 370.4 BAU/mL; range, 1.0-8977.3 BAU/mL) relative to just prior to D3 (average = 25.0 BAU/mL; range, 1.0-683.8 BAU/mL) and achieved higher levels than peak levels after the first two doses (average = 144.8 BAU/mL; range, 1.0-4,284.1 BAU/mL). D3 response positively correlated with mRNA-1273, a > 10-fold change from baseline for the two-dose series, switching from BNT162b2 to mRNA-1273 for D3, and treatment with elotuzumab and an immunomodulatory agent. Lower antibody levels prior to D3, poorer overall response to first two doses, and ruxolitinib or anti-CD38 monoclonal antibody treatment negatively correlated with D3 response. Our results show encouraging activity of the third vaccine, even among patients who failed to respond to the first two vaccinations. The finding of specific factors that predict COVID-19 antibody levels will help advise patients and healthcare professionals on the likelihood of responses to further vaccinations.

Indexed as

COVID-19Infectious DiseaseMultiple MyelomaSARS-CoV-2Vaccine booster dose

Identifiers

PMID36530752
PMCPMC9744558
OpenAlexW4311400743

What OpenQuestion holds

Textmetadata
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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.