Antibody Response to COVID-19 mRNA Vaccine in Patients With Lung Cancer After Primary Immunization and Booster: Reactivity to the SARS-CoV-2 WT Virus and Omicron Variant

PURPOSETo examine COVID-19 mRNA vaccine-induced binding and neutralizing antibody responses in patients with non-small-cell lung cancer (NSCLC) to SARS-CoV-2 614D (wild type [WT]) strain and variants of concern after the primary 2-dose and booster vaccination.METHODSEighty-two patients with NSCLC an...

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Published inJournal of clinical oncology Vol. 40; no. 33; pp. 3808 - 3816
Main Authors Valanparambil, Rajesh M., Carlisle, Jennifer, Linderman, Susanne L., Akthar, Akil, Millett, Ralph Linwood, Lai, Lilin, Chang, Andres, McCook-Veal, Ashley A., Switchenko, Jeffrey, Nasti, Tahseen H., Saini, Manpreet, Wieland, Andreas, Manning, Kelly E., Ellis, Madison, Moore, Kathryn M., Foster, Stephanie L., Floyd, Katharine, Davis-Gardner, Meredith E., Edara, Venkata-Viswanadh, Patel, Mit, Steur, Conor, Nooka, Ajay K., Green, Felicia, Johns, Margaret A., O'Brein, Fiona, Shanmugasundaram, Uma, Zarnitsyna, Veronika I., Ahmed, Hasan, Nyhoff, Lindsay E., Mantus, Grace, Garett, Michael, Edupuganti, Srilatha, Behra, Madhusmita, Antia, Rustom, Wrammert, Jens, Suthar, Mehul S., Dhodapkar, Madhav V., Ramalingam, Suresh, Ahmed, Rafi
Format Journal Article
LanguageEnglish
Published United States Wolters Kluwer Health 20.11.2022
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Summary:PURPOSETo examine COVID-19 mRNA vaccine-induced binding and neutralizing antibody responses in patients with non-small-cell lung cancer (NSCLC) to SARS-CoV-2 614D (wild type [WT]) strain and variants of concern after the primary 2-dose and booster vaccination.METHODSEighty-two patients with NSCLC and 53 healthy volunteers who received SARS-CoV-2 mRNA vaccines were included in the study. Blood was collected longitudinally, and SARS-CoV-2-specific binding and neutralizing antibody responses were evaluated by Meso Scale Discovery assay and live virus Focus Reduction Neutralization Assay, respectively.RESULTSA majority of patients with NSCLC generated binding and neutralizing antibody titers comparable with the healthy vaccinees after mRNA vaccination, but a subset of patients with NSCLC (25%) made poor responses, resulting in overall lower (six- to seven-fold) titers compared with the healthy cohort (P = < .0001). Although patients age > 70 years had lower immunoglobulin G titers (P = < .01), patients receiving programmed death-1 monotherapy, chemotherapy, or a combination of both did not have a significant impact on the antibody response. Neutralizing antibody titers to the B.1.617.2 (Delta), B.1.351 (Beta), and in particular, B.1.1.529 (Omicron) variants were significantly lower (P = < .0001) compared with the 614D (WT) strain. Booster vaccination led to a significant increase (P = .0001) in the binding and neutralizing antibody titers to the WT and Omicron variant. However, 2-4 months after the booster, we observed a five- to seven-fold decrease in neutralizing titers to WT and Omicron viruses.CONCLUSIONA subset of patients with NSCLC responded poorly to the SARS-CoV-2 mRNA vaccination and had low neutralizing antibodies to the B.1.1.529 Omicron variant. Booster vaccination increased binding and neutralizing antibody titers to Omicron, but antibody titers declined after 3 months. These data highlight the concern for patients with cancer given the rapid spread of SARS-CoV-2 Omicron variant.
Bibliography:Rafi Ahmed, PhD, Emory Vaccine Center, Georgia Research Alliance Eminent Scholar, Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322; e-mail: rahmed@emory.edu.*R.M.V. and J.C. contributed equally to this work. S.R. and R.A. contributed equally to this work.
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ISSN:0732-183X
1527-7755
1527-7755
DOI:10.1200/JCO.21.02986