Predictors of poor seroconversion and adverse events to SARS-CoV-2 mRNA BNT162b2 vaccine in cancer patients on active treatment

Eur J Cancer. 2021 Dec:159:105-112. doi: 10.1016/j.ejca.2021.09.030. Epub 2021 Oct 11.

Abstract

Purpose: Initial findings in patients with cancer suggest a lower seroconversion to SARS-CoV-2 vaccination possibly related to myelo-immunosuppressive therapies. We conducted a prospective study to assess factors predicting poor seroconversion and adverse events following immunisation (AEFI) to the BNT162b2 vaccine in patients on active treatment.

Patients and methods: Cancer patients, candidates to two doses of BNT162b2 SARS-CoV-2 vaccination, were enrolled. Patients on active surveillance served as controls. The primary endpoint was poor seroconversion (anti S1/S2 IgG < 25 AU/mL) after 21 days from the second dose.

Results: Between March and July 2021, 320 subjects were recruited, and 291 were assessable. The lack of seroconversion at 21 days from the second dose was 1.6% (95% CI, 0.4-8.7) on active surveillance, 13.9% (8.2-21.6) on chemotherapy, 11.4% (5.1-21.3) on hormone therapy, 21.7% (7.5-43.7) on targeted therapy and 4.8% (0.12-23.8) on immune-checkpoint-inhibitors (ICI). Compared to controls, the risk of no IgG response was greater for chemotherapy (p = 0.033), targeted therapy (0.005) and hormonotherapy (p = 0.051). Lymphocyte count < 1 × 109/L (p = 0.04) and older age (p = 0.03) also significantly predicted poor seroconversion. Overall, 43 patients (14.8%) complained of AEFI, mostly of mild grade. Risk of AEFI was greater in females (p = 0.001) and younger patients (p = 0.009).

Conclusion: Chemotherapy, targeted therapy, hormone therapy, lymphocyte count < 1 × 109/L, and increasing age predict poor seroconversion after two doses of BNT162b2 in up to 20% of patients, indicating the need for a third dose and long-term serological testing in non-responders. AEFI occur much more frequently in women and younger subjects who may benefit from preventive medications. CLINICALTRIALS.

Gov identifier: NCT04932863.

Keywords: Antibody responses to the BNT162b2 vaccine; COVID-19 vaccine in cancer patients; Cancer biological treatment; Cancer chemotherapy; Cancer hormone therapy; Cancer immunotherapy; Cancer target therapy; Immunogenicity; SARS-CoV-2 vaccine; SARS-CoV-2 vaccine adverse effects.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Antibodies, Viral / blood*
  • BNT162 Vaccine / administration & dosage*
  • BNT162 Vaccine / adverse effects
  • BNT162 Vaccine / immunology
  • Biomarkers / blood
  • COVID-19 / immunology
  • COVID-19 / prevention & control*
  • COVID-19 / virology
  • Case-Control Studies
  • Female
  • Humans
  • Immunogenicity, Vaccine*
  • Male
  • Middle Aged
  • Neoplasms / diagnosis
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • Prospective Studies
  • Risk Factors
  • SARS-CoV-2 / immunology*
  • SARS-CoV-2 / pathogenicity
  • Seroconversion
  • Time Factors
  • Treatment Outcome
  • Vaccination* / adverse effects
  • Vaccine Efficacy*

Substances

  • Antibodies, Viral
  • Biomarkers
  • BNT162 Vaccine

Associated data

  • ClinicalTrials.gov/NCT04932863