Evidence map›Paper›PMID 34778797›Full record

ArticleBlood cancer discovery2021

Disease- and Therapy-Specific Impact on Humoral Immune Responses to COVID-19 Vaccination in Hematologic Malignancies.

David J Chung, Gunjan L Shah, Sean M Devlin, Lakshmi V Ramanathan, Sital Doddi, Melissa S Pessin, Elizabeth Hoover, LeeAnn T Marcello, Jennifer C Young, Sawsan R Boutemine and 14 more

Open access · bronzeAbstract readComment
In one paragraph

Article in Blood cancer discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 5 pooled it
4.7field-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

52 citing papers in PubMed, 5 syntheses or guidelines pooled it, 74 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 8 institutions in 1 country.

David J ChungAdult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center (MSKCC), New York, New York. chungd1@mskcc.org.ORCID 0000-0003-0469-839X
Gunjan L ShahAdult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center (MSKCC), New York, New York.ORCID 0000-0002-9977-0456
Sean M DevlinDepartment of Epidemiology and Biostatistics, MSKCC, New York, New York.
Lakshmi V RamanathanDepartment of Laboratory Medicine, MSKCC, New York, New York.
Sital DoddiDepartment of Laboratory Medicine, MSKCC, New York, New York.
Melissa S PessinDepartment of Laboratory Medicine, MSKCC, New York, New York.ORCID 0000-0003-3990-6494
Elizabeth HooverAdult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center (MSKCC), New York, New York.
LeeAnn T MarcelloAdult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center (MSKCC), New York, New York.ORCID 0000-0002-9801-5029
Jennifer C YoungAdult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center (MSKCC), New York, New York.
Sawsan R BoutemineLymphoma Service, Department of Medicine, MSKCC, New York, New York.
Edith SerranoMyeloma Service, Department of Medicine, MSKCC, New York, New York.
Saumya SharanLeukemia Service, Department of Medicine, MSKCC, New York, New York.
Saddia MomotajLeukemia Service, Department of Medicine, MSKCC, New York, New York.
Lauren MargetichLeukemia Service, Department of Medicine, MSKCC, New York, New York.
Christina D BravoCenter for Hematologic Malignancies, MSKCC, New York, New York.
Genovefa A PapanicolaouInfectious Disease Service, Department of Medicine, MSKCC, New York, New York.
Mini KambojInfectious Disease Service, Department of Medicine, MSKCC, New York, New York.
Anthony R MatoDepartment of Medicine, Weill Cornell Medical College, New York, New York.
Lindsey E RoekerDepartment of Medicine, Weill Cornell Medical College, New York, New York.
Malin HultcrantzDepartment of Medicine, Weill Cornell Medical College, New York, New York.
Sham MailankodyDepartment of Medicine, Weill Cornell Medical College, New York, New York.
Alexander M LesokhinDepartment of Medicine, Weill Cornell Medical College, New York, New York.
Santosha A Vardhana *Department of Medicine, Weill Cornell Medical College, New York, New York.ORCID 0000-0002-3100-1298
David A Knorr *Department of Medicine, Weill Cornell Medical College, New York, New York.
Cornell University · USManhattan Scientifics (United States) · USMemorial Sloan Kettering Cancer Center · USInfectious Disease Consultants · USCancer Research And Biostatistics · USLymphoma Research Foundation · USManhattan School of Music · USNew York State Department of State · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
T LYMPHOCYTE SUBSET FUNCTION POST-TRANSPLANTATIONP01CA023766 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SCHEINBERG, DAVID A · 1985 to 2023
$59.0M
Fc-enhanced CD40 agonist antibodies for immune modulation of the tumor microenvironmentK08CA248966 · NCI · ROCKEFELLER UNIVERSITY · PI KNORR, DAVID A. · 2020 to 2022
$636k
NCI NIH HHS K08 CA248966NCI NIH HHS P01 CA023766NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Coronavirus disease-19 (COVID-19) vaccine response data for patients with hematologic malignancy, who carry high risk for severe COVID-19 illness, are incomplete. In a study of 551 hematologic malignancy patients with leukemia, lymphoma, and multiple myeloma, anti-SARS-CoV-2 spike IgG titers and neutralizing activity were measured at 1 and 3 months from initial vaccination. Compared with healthy controls, patients with hematologic malignancy had attenuated antibody titers at 1 and 3 months. Furthermore, patients with hematologic malignancy had markedly diminished neutralizing capacity of 26.3% at 1 month and 43.6% at 3 months, despite positive seroconversion rates of 51.5% and 68.9% at the respective time points. Healthy controls had 93.2% and 100% neutralizing capacity at 1 and 3 months, respectively. Patients with leukemia, lymphoma, and multiple myeloma on observation had uniformly blunted responses. Treatment with Bruton tyrosine kinase inhibitors, venetoclax, phosphoinositide 3-kinase inhibitors, anti-CD19/CD20-directed therapies, and anti-CD38/B-cell maturation antigen-directed therapies substantially hindered responses, but single-agent immunomodulatory agents did not. Significance: Patients with hematologic malignancy have compromised COVID-19 vaccine responses at baseline that are further suppressed by active therapy, with many patients having insufficient neutralizing capacity despite positive antibody titers. Refining vaccine response parameters is critical to guiding clinical care, including the indication for booster vaccines, for this vulnerable population.

Indexed as

COVID-19Hematologic NeoplasmsBNT162 VaccineCOVID-19 VaccinesHumansImmunity, HumoralPhosphatidylinositol 3-KinasesSARS-CoV-2VaccinationBNT162 VaccineCOVID-19 VaccinesPhosphatidylinositol 3-Kinases

Identifiers

PMID34778797
PMCPMC8580617
OpenAlexW3199004246

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.