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Impaired immunogenicity after vaccination for SARS-CoV-2 in patients with gastrointestinal cancer: does tumor entity
Malte Benedikt Monin1,2, Jens Gabriel Gorny1, Moritz Berger3
1Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.
Background:
SARS-CoV-2 immunogenicity in patients with gastrointestinal cancer (GI cancer) following second and third vaccination was analyzed.
Methods:
A total of 125 patients under active anticancer therapy or in follow-up care were included in this prospective study. Seroprevalence of SARS-CoV-2 anti-spike and surrogate neutralization antibodies (NABs) was measured.
Results:
Four weeks after second vaccination, adequate titers of SARS-CoV-2 anti-spike immunoglobulin G (IgG) [≥282.0 binding antibody units (BAU)/mL] were found in 62.2% of patients under treatment versus 96.3% of patients in follow-up care (P<0.01). Sufficient titers of SARS-CoV-2 surrogate NAB (≥85.0%) were found in 32.7% of patients under treatment versus 70.6% in follow-up care (P<0.01). Titers of SARS-CoV-2 anti-spike IgG were especially low in patients with colorectal cancer (CRC). For SARS-CoV-2 surrogate NAB, patients with hepatocellular carcinoma (HCC) and with pancreaticobiliary cancer showed the lowest titers (P<0.01). SARS-CoV-2 anti-spike IgG and SARS-CoV-2 surrogate NAB were associated with a correlation coefficient of 0.93. Reaching a titer of SARS-CoV-2 anti-spike IgG ≥482.0 BAU/mL, protective levels of SARS-CoV-2 surrogate NAB (≥85.0%) could be assumed. Following booster vaccination, all patients reached effective antibody titers.
Conclusions:
Patients with active GI cancer showed impaired immunogenicity after second SARS-CoV-2 vaccination which was overcome by booster vaccination. Our findings were tumor-related and pronounced in patients with CRC and HCC. Waning immunity over time and antibody escape phenomena by variant of concern Omicron must be considered in these especially vulnerable patients.
Insights
Gastrointestinal cancer patients showed lower SARS-CoV-2 antibody levels after two vaccine doses, especially those undergoing treatment. Booster vaccination restored effective immunity in all patients, highlighting the need for vigilance against waning immunity and variants.
Area of Science:
- Immunology
- Oncology
- Vaccinology
Background:
- Analyzing SARS-CoV-2 immunogenicity in gastrointestinal (GI) cancer patients post-vaccination.
- Assessing immune response in patients undergoing active anticancer therapy versus those in follow-up care.
Purpose of the Study:
- To evaluate SARS-CoV-2 antibody and neutralization antibody titers after second and third vaccinations in GI cancer patients.
- To identify specific cancer types (e.g., colorectal, hepatocellular) with potentially impaired vaccine responses.
Main Methods:
- Prospective study of 125 GI cancer patients.
- Measurement of SARS-CoV-2 anti-spike immunoglobulin G (IgG) and surrogate neutralization antibodies (NABs).
Main Results:
- Significantly lower antibody titers observed in patients under active treatment compared to those in follow-up care after the second dose.
- Colorectal cancer (CRC) patients showed low anti-spike IgG, while hepatocellular carcinoma (HCC) and pancreaticobiliary cancer patients had low NABs.
- Booster vaccination led to effective antibody titers in all patients, with strong correlation between IgG and NABs.
Conclusions:
- Active GI cancer patients exhibit impaired immunogenicity after initial SARS-CoV-2 vaccination, which is improved by booster doses.
- Tumor type influences immune response, with CRC and HCC patients being particularly vulnerable.
- Consideration of waning immunity and Omicron variant escape is crucial for this patient group.
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