COVID-19 and Influenza Booster Vaccination Elicits Robust Antibody Responses in Patients with Primary Brain Tumors Comparable to Healthy Adults

<b>Background</b>: Patients with primary brain tumors face profound disease- and treatment-related immunosuppression, placing them at high risk for severe infections. Their capacity to mount protective immune responses to vaccination, particularly to repeated antigen exposures such as COVID-19 boosters, remains critically under-defined, leading to uncertainty in clinical practice. <b>Methods</b>: In this prospective cohort study, we analyzed humoral responses to seasonal COVID-19 (mRNA-based) and influenza vaccination in 17 patients with primary brain tumors (recruited from an initial cohort of 37) who received a booster shot, and 19 healthy controls. Serum samples were collected before (T1) and 30 ± 2 days after (T2) vaccination to quantify SARS-CoV-2 anti-Spike (S) IgG and anti-Influenza IgG titers. <b>Results</b>: Despite ongoing chemotherapy in 47% of patients, baseline anti-S antibody titers were comparable between groups. Following the booster, median anti-S titers increased significantly and to a similar magnitude in both patients (from 5030 to 18,500 BAU/mL; IQR: 13,885-24,420) and controls (from 4429 to 20,200 BAU/mL; IQR: 11,075-26,680; <i>p</i> = 0.6137, Mann-Whitney U test). Only two heavily pre-treated patients showed no booster response. All participants showed sero-positivity to Anti-Influenza IgG at baseline. For the primary brain tumor cohort, a significant increase for anti-Influenza IgG at T2 was observed (<i>p</i> = 0.0002). Mean antibody titers did not differ between both cohorts. <b>Conclusions</b>: Our findings provide evidence that patients with primary brain tumors can mount robust recall immunity to mRNA vaccines, addressing clinical uncertainty about booster efficacy in this population. These data provide a strong rationale for prioritizing booster vaccinations in this vulnerable population and argue for the inclusion of these patients in future pivotal vaccine trials.

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Journal
Cancers
Published
2026-02-02
DOI
https://doi.org/10.3390/cancers18030494
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
0.00

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article

COVID-19 and Influenza Booster Vaccination Elicits Robust Antibody Responses in Patients with Primary Brain Tumors Comparable to Healthy Adults

Giorgio Cappello, Ulf Dittmer, Sied Kebir, Yahya Ahmadipour et al.
Cancers
SARS-CoV-2 and COVID-19 Research
article

COVID-19 and Influenza Booster Vaccination Elicits Robust Antibody Responses in Patients with Primary Brain Tumors Comparable to Healthy Adults

Giorgio Cappello, Ulf Dittmer, Sied Kebir, Yahya Ahmadipour, Leon Jekel, Vu Thuy Khanh Le‐Trilling, B Scheffler, Teresa Schmidt, Kathrin Kizina, Christoph Oster, Laurèl Rauschenbach, Martin Glas, Lucia Asar, Ulrich Sure, Melanie Fiedler, Christoph Kleinschnitz, Jana Grieger, Leandra Grzib
article en

Abstract

<b>Background</b>: Patients with primary brain tumors face profound disease- and treatment-related immunosuppression, placing them at high risk for severe infections. Their capacity to mount protective immune responses to vaccination, particularly to repeated antigen exposures such as COVID-19 boosters, remains critically under-defined, leading to uncertainty in clinical practice. <b>Methods</b>: In this prospective cohort study, we analyzed humoral responses to seasonal COVID-19 (mRNA-based) and influenza vaccination in 17 patients with primary brain tumors (recruited from an initial cohort of 37) who received a booster shot, and 19 healthy controls. Serum samples were collected before (T1) and 30 ± 2 days after (T2) vaccination to quantify SARS-CoV-2 anti-Spike (S) IgG and anti-Influenza IgG titers. <b>Results</b>: Despite ongoing chemotherapy in 47% of patients, baseline anti-S antibody titers were comparable between groups. Following the booster, median anti-S titers increased significantly and to a similar magnitude in both patients (from 5030 to 18,500 BAU/mL; IQR: 13,885-24,420) and controls (from 4429 to 20,200 BAU/mL; IQR: 11,075-26,680; <i>p</i> = 0.6137, Mann-Whitney U test). Only two heavily pre-treated patients showed no booster response. All participants showed sero-positivity to Anti-Influenza IgG at baseline. For the primary brain tumor cohort, a significant increase for anti-Influenza IgG at T2 was observed (<i>p</i> = 0.0002). Mean antibody titers did not differ between both cohorts. <b>Conclusions</b>: Our findings provide evidence that patients with primary brain tumors can mount robust recall immunity to mRNA vaccines, addressing clinical uncertainty about booster efficacy in this population. These data provide a strong rationale for prioritizing booster vaccinations in this vulnerable population and argue for the inclusion of these patients in future pivotal vaccine trials.

CancersVol. 18(3)
German Cancer Research Center (DE), Heidelberg University (DE), University Hospital Bonn (DE), Düsseldorf University Hospital (DE), Katholisches Klinikum Lünen/Werne , St.-Marien-Hospital Lünen (DE), Essen University Hospital (DE), West German Heart and Vascular Center Essen (DE), Heinrich Heine University Düsseldorf (DE), University of Duisburg-Essen (DE)
Novocure, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Universität Duisburg-Essen, Servier, Medac, Daiichi Sankyo Europe, Cilag
Reduced inequalities
Openalex Percentile: Top 67%
SARS-CoV-2 and COVID-19 Research
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