Evidence map›Paper›PMID 35811461›Full record

ArticleCancer2022

Seroconversion and outcomes after initial and booster COVID-19 vaccination in adults with hematologic malignancies.

Thomas A Ollila, Rebecca H Masel, John L Reagan, Shaolei Lu, Ralph D Rogers, Kimberly J Paiva, Rashida Taher, Ella Burguera-Couce, Adam S Zayac, Inna Yakirevich and 3 more

Open access · greenAbstract read
In one paragraph

Article in Cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
4.3field-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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 44 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

13 authors at 3 institutions in 1 country.

Thomas A OllilaDepartment of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island, USA.ORCID 0000-0003-0102-6491
Rebecca H MaselDepartment of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island, USA.
John L ReaganDepartment of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island, USA.
Shaolei LuDepartment of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island, USA.
Ralph D RogersDepartment of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island, USA.
Kimberly J PaivaDepartment of Pathology and Laboratory Medicine, Rhode Island Hospital, Providence, Rhode Island, USA.
Rashida TaherDivision of Hematology-Oncology, Rhode Island Hospital, Providence, Rhode Island, USA.
Ella Burguera-CouceWarren Alpert Medical School of Brown University, Providence, Rhode Island, USA.
Adam S ZayacDepartment of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island, USA.ORCID 0000-0002-7591-2069
Inna YakirevichDivision of Hematology-Oncology, Rhode Island Hospital, Providence, Rhode Island, USA.
Rabin NiroulaDepartment of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island, USA.
Peter BarthDepartment of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island, USA.ORCID 0000-0003-2216-8376
Adam J OlszewskiDepartment of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island, USA.ORCID 0000-0002-6472-6658
Brown University · USProvidence College · USRhode Island Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with hematologic malignancies have impaired humoral immunity secondary to their malignancy and its treatment, placing them at risk of severe coronavirus disease-19 (COVID-19) infection and reduced response to vaccination.

methodsThe authors retrospectively analyzed serologic responses to initial and booster COVID-19 vaccination in 378 patients with hematologic malignancy and subsequently tracked COVID-19-related outcomes.

resultsSeroconversion occurred in 181 patients (48%) after initial vaccination; patients who had active malignancy or those who were recently treated with a B-cell-depleting monoclonal antibody had the lowest rates of seroconversion. For initial nonresponders to vaccination, seroconversion after a booster dose occurred in 48 of 85 patients (56%). The seroconversion rate after the booster was similar for patients on (53%) and off (58%) active therapy (p = .82). Thirty-three patients (8.8%) developed a COVID-19 infection, and there were three COVID-19-related deaths (0.8%). Although no significant association was observed between postvaccination seroconversion and the incidence of COVID-19 infection, no patient with seroconversion died from COVID-19, and no patient who received tixagevimab/cilgavimab (N = 25) was diagnosed with a COVID-19 infection.

conclusionsBooster vaccinations can promote seroconversion in a significant proportion of patients who are seronegative after the initial vaccination course regardless of the specific vaccine or on/off treatment status at the time of revaccination. Although postvaccination seroconversion may not be associated with a decrease in any (including asymptomatic) COVID-19 infection, the authors' experience suggested that effective vaccination (including a booster), supplemented by passive immunization using tixagevimab/cilgavimab in case of lack of seroconversion, effectively eliminated the risk of COVID-19 death in the otherwise high-risk population. LAY SUMMARY: Patients with hematologic malignancy, especially lymphoma, have an impaired response to coronavirus disease 2019 (COVID-19) vaccination. In this single-institution review, less than one half of the patients studied made detectable antibodies. For those who did not make detectable antibodies after initial vaccination, over one half (65%) were able to produce antibodies after booster vaccination. By the end of February 2022, 33 of the original 378 patients had a documented COVID-19 infection. The only deaths from COVID-19 were in those who had undetectable antibodies, and no patient who received prophylactic antibody therapy developed a COVID-19 infection.

Indexed as

COVID-19Hematologic NeoplasmsAdultAntibodies, MonoclonalAntibodies, ViralCOVID-19 VaccinesHepatitis B VaccinesHumansRetrospective StudiesSeroconversionVaccinationAntibodies, MonoclonalAntibodies, ViralcilgavimabCOVID-19 VaccinesHepatitis B Vaccinestixagevimabboostercancercoronavirushumoral immunitylymphoma

Identifiers

PMID35811461
PMCPMC9349722
OpenAlexW4285008916

What OpenQuestion holds

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Registered trials

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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.