Impact of SARS-CoV-2 infection on bispecific antibody treatment in patients with B-cell lymphoproliferative disorders

Despite advances in vaccination and the use of antiviral treatments, patients with hematologic malignancies, including B-cell lymphoproliferative disorders, are particularly vulnerable to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. The recent introduction of bispecific antibodies (BsAbs) in the treatment algorithm of relapsed/refractory B-cell non-Hodgkin lymphoma (B-NHL) has raised concerns regarding their impact on COVID-19 outcomes. This study aimed to evaluate the impact of SARS-CoV-2 infection on treatment outcomes in patients receiving BsAbs. We assessed the severity of COVID-19 and SARS-CoV-2 serostatus, with antibody titers measured before, during, and after BsAbs administration. A total of 109 patients with B-NHL treated with BsAbs from March 2020 to January 2023 were included. SARS-CoV-2 infection was observed in 56 patients (51%), with 36% experiencing prolonged viral shedding, causing therapy delays in 78% of patients and permanent discontinuations in 19%. Regarding COVID-19 severity, 36% of patients presented moderate, 20% severe, and 12% critical disease. Seven patients (13%) died owing to COVID-19 pneumonia. Similar to observations with anti-CD20 monoclonal antibodies, BsAbs were associated with negative antispike serostatus for at least 6 months after treatment completion. Importantly, this lack of seroconversion was linked with severe disease and increased mortality. These findings underscore important considerations for the management of patients receiving BsAbs.

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Publication Details

Journal
Blood Advances
Published
2025-05-22
DOI
https://doi.org/10.1182/bloodadvances.2024015406
Citations
3
Primary Topic
Lymphoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
4.41

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Impact of SARS-CoV-2 infection on bispecific antibody treatment in patients with B-cell lymphoproliferative disorders

Adaia Albasanz‐Puig, Ana Marín‐Niebla, Anna Falcó-Roget, Josu Iraola‐Truchuelo et al.
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article

Impact of SARS-CoV-2 infection on bispecific antibody treatment in patients with B-cell lymphoproliferative disorders

Adaia Albasanz‐Puig, Ana Marín‐Niebla, Anna Falcó-Roget, Josu Iraola‐Truchuelo, Juliana Esperalba, Moraima Jiménez, Marta Crespo, Gloria Iacoboni, Cecilia Carpio, Isabel Ruíz-Camps, Tomás García-Cerecedo, Francesc Bosch, Cristina Andrés, Andrés Antón, Ángel Serna, Ainara Ferrero, Vı́ctor Navarro, Marc Bosch, Pau Abrisqueta, Cristina García-Herce
article en
3 citations

Abstract

Despite advances in vaccination and the use of antiviral treatments, patients with hematologic malignancies, including B-cell lymphoproliferative disorders, are particularly vulnerable to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. The recent introduction of bispecific antibodies (BsAbs) in the treatment algorithm of relapsed/refractory B-cell non-Hodgkin lymphoma (B-NHL) has raised concerns regarding their impact on COVID-19 outcomes. This study aimed to evaluate the impact of SARS-CoV-2 infection on treatment outcomes in patients receiving BsAbs. We assessed the severity of COVID-19 and SARS-CoV-2 serostatus, with antibody titers measured before, during, and after BsAbs administration. A total of 109 patients with B-NHL treated with BsAbs from March 2020 to January 2023 were included. SARS-CoV-2 infection was observed in 56 patients (51%), with 36% experiencing prolonged viral shedding, causing therapy delays in 78% of patients and permanent discontinuations in 19%. Regarding COVID-19 severity, 36% of patients presented moderate, 20% severe, and 12% critical disease. Seven patients (13%) died owing to COVID-19 pneumonia. Similar to observations with anti-CD20 monoclonal antibodies, BsAbs were associated with negative antispike serostatus for at least 6 months after treatment completion. Importantly, this lack of seroconversion was linked with severe disease and increased mortality. These findings underscore important considerations for the management of patients receiving BsAbs.

Blood AdvancesVol. 9(16)
Hebron University (PS), Universitat Autònoma de Barcelona (ES), Hospital Universitari Arnau de Vilanova (ES), Vall d'Hebron Institut de Recerca (ES), Hospital Arnau de Vilanova (ES), Vall d'Hebron Hospital Universitari (ES), Vall d'Hebron Institute of Oncology (ES)
Pfizer, AstraZeneca, Gilead Sciences, Celgene, BeiGene, Incyte, Instituto de Salud Carlos III
Good health and well-being
Openalex Percentile: Top 6%
Lymphoma Diagnosis and Treatment
4.41
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