Vaccination against
COVID-19 is critical for immuno-compromised individuals, including patients with
cancer. Systemic reactogenicity, a manifestation of the innate immune response to
vaccines, occurs in up to 69% of patients following vaccination with
RNA-based
COVID-19 vaccines.
Tumor regression can occur following an intense immune-inflammatory response and novel strategies to treat
cancer rely on manipulating the host immune system. Here, we report
spontaneous regression of metastatic salivary gland myoepithelial
carcinoma in a patient who experienced grade 3 systemic reactogenicity, following vaccination with the
mRNA-1273 COVID-19 vaccine. Histological and immunophenotypic inspection of the postvaccination lung biopsy specimens showed a massive inflammatory infiltrate with scant embedded
tumor clusters (<5%). Highly multiplexed imaging mass cytometry showed that the postvaccination lung
metastasis samples had remarkable immune cell infiltration, including CD4+ T cells, CD8+ T cells, natural killer cells, B cells, and dendritic cells, which contrasted with very low levels of these cells in the prevaccination primary
tumor and lung
metastasis samples. CT scans obtained 3, 6, and 9 months after the second
vaccine dose demonstrated persistent
tumor shrinkage (50%, 67%, and 73% reduction, respectively), suggesting that vaccination stimulated anticancer immunity. Insight: This case suggests that the
mRNA-1273 COVID-19 vaccine stimulated anticancer immunity and
tumor regression.