# Antibody Responses to SARS-CoV-2 in Cancer Patients in New York City During the 2020 Wave of the COVID-19 Pandemic

**Authors:** Maria Gianniki, Yuxuan Li, William Glembocki, Marilia Bernardes, Yoginder Hinwar, Kaitlin Walsh, Genovefa Papanicolaou

PMC · DOI: 10.7759/cureus.102541 · Cureus · 2026-01-29

## TL;DR

This study found that most cancer patients in NYC developed antibodies after contracting COVID-19 in 2020, but those on B-cell-depleting therapies had weaker and less common responses.

## Contribution

The study provides new insights into how different cancer types and treatments affect antibody responses to SARS-CoV-2 in unvaccinated patients.

## Key findings

- 87% of cancer patients had an early antibody response to SARS-CoV-2.
- Only 50% of patients on B-cell-depleting therapies developed antibodies, with significantly lower titers.
- IgG titers declined by 14.437 AU/mL per day after diagnosis.

## Abstract

Introduction: New York City was the epicenter of the first wave of the COVID-19 pandemic, and cancer patients were among the most vulnerable groups. We characterized antibody response in a diverse cohort of cancer patients prior to the availability of COVID-19 therapeutics. We report: (1) antibody response to COVID-19 by cancer type; (2) trend of SARS-CoV-2 IgG spike antibodies over time in cancer patients with COVID-19 diagnosis during 2020-2021.

Methods: Single-center, prospective, observational study of patients treated for cancer at Memorial Sloan Kettering Cancer Center with symptomatic, laboratory-confirmed COVID-19. Serial blood specimens were collected after COVID-19 diagnosis and before administration of any COVID-19 vaccine or monoclonal antibody. IgG was determined using the AdviseDx SARS-CoV-2 IgG II assay. Antibody response was defined as a titer ≥50 AU/mL. Early antibody response was defined as <14 weeks, and late antibody response as >14 weeks after COVID-19 diagnosis. Group comparisons were performed using the Wilcoxon rank-sum test, while Fisher’s exact or chi-squared tests and ANOVA were used for categorical comparisons. A locally estimated scatterplot smoothing technique and a linear mixed-effects model were applied to assess the trend in IgG titers over time.

Results: Of 245 patients analyzed, 127 (51.9%) had solid tumors and 118 (48.1%) hematologic malignancies. Among patients with hematologic malignancies, 15 received B-cell-depleting therapies within 6 months of COVID-19 diagnosis. Overall, 181 (87%) patients had early antibody response, including 97 (92%) patients with solid tumors, 77 (88%) with hematologic malignancies without B-cell-depleting therapies, and 7 (50%) with hematologic malignancies who received B-cell-depleting therapies. The magnitude of early antibody response was significantly lower in patients who received B-cell-depleting therapies compared to both other groups. A total of 452 specimens were analyzed to evaluate the trend of IgG titers over time. A measurable decline is observed over time, with an estimated 14.437 AU/mL decrease per day post-COVID-19 diagnosis (p <0.001).

Conclusion: Overall, 87% of cancer patients had an early antibody response to COVID-19. Only 50% of patients with hematologic malignancies who received B-cell-depleting therapies developed an antibody response, and IgG titers were significantly lower in this group compared to both patients with solid tumors and patients with hematologic malignancies without B-cell-depleting therapies. We observed a progressive decline in IgG titers over time, with an estimated decrease of 14.437 AU/mL per day post-COVID-19 diagnosis. These findings offer valuable insights into antibody responses in cancer patients following COVID-19 infection.

## Linked entities

- **Diseases:** cancer (MONDO:0004992), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** N (nucleocapsid phosphoprotein) [NCBI Gene 43740575], TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, ABR (ABR activator of RhoGEF and GTPase) [NCBI Gene 29] {aka MDB}, S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}
- **Diseases:** infected (MESH:D007239), COVID-19 (MESH:D000086382), deaths (MESH:D003643), viral infections (MESH:D014777), Solid (MESH:D018250), multiple myeloma (MESH:D009101), Solid tumors (MESH:D009369), BCD (MESH:C535440), impaired immunity (MESH:D020274), HM (MESH:D019337), respiratory (MESH:D012131)
- **Chemicals:** rituximab (MESH:D000069283), obinutuzumab (MESH:C543332), BCD (-), methotrexate (MESH:D008727)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12949483/full.md

## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12949483/full.md

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Source: https://tomesphere.com/paper/PMC12949483