Immunogenicity of anti-SARS-CoV-2 Comirnaty vaccine in patients with lymphomas and myeloma who underwent autologous stem cell transplantation - Scorecard - MDSpire

Immunogenicity of anti-SARS-CoV-2 Comirnaty vaccine in patients with lymphomas and myeloma who underwent autologous stem cell transplantation

  • By

  • Marco Salvini

  • Fabrizio Maggi

  • Camilla Damonte

  • Lorenzo Mortara

  • Antonino Bruno

  • Barbara Mora

  • Marco Brociner

  • Roberta Mattarucchi

  • Alessia Ingrassia

  • Davide Sirocchi

  • Benedetta Bianchi

  • Stefania Agnoli

  • Matteo Gallazzi

  • Michele Merli

  • Andrea Ferrario

  • Raffaella Bombelli

  • Daniela Barraco

  • Andreina Baj

  • Lorenza Bertù

  • Paolo A. Grossi

  • Francesco Passamonti

  • October 11, 2021

  • 0 min

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Clinical Scorecard: Efficacy of the Comirnaty Vaccine Against SARS-CoV-2 in Lymphoma and Myeloma Patients Post-Autologous Stem Cell Transplantation

At a Glance

CategoryDetail
ConditionHematological malignancies (lymphoma and myeloma) post-autologous stem cell transplantation
Key MechanismsHumoral and cellular immune responses to SARS-CoV-2 mRNA vaccination (Comirnaty) assessed by antibody titers and T-cell assays
Target PopulationAdult patients with hematological malignancies who underwent autologous stem cell transplantation
Care SettingHematology department, post-transplant outpatient follow-up

Key Highlights

  • 87% of patients developed a humoral immune response after two doses of Comirnaty vaccine, with median antibody titer of 747 BAU/ml.
  • Vaccination failure was significantly associated with being on active therapy at time of vaccination and not having ASCT as last treatment.
  • Seronegative patients showed significantly lower spike-specific CD8+IFNγ+ and CD4+ T-cell responses compared to seropositive patients.

Guideline-Based Recommendations

Diagnosis

  • Evaluate humoral immunity using anti-SARS-CoV-2 S1/S2 IgG test with cutoff >33.8 BAU/ml for positivity.
  • Assess cell-mediated immunity in seronegative patients using FACS and ELISpot assays for spike-specific T-cell responses.

Management

  • Prioritize mRNA vaccination (Comirnaty) for patients with hematological malignancies, including those post-ASCT.
  • Consider timing of vaccination relative to ASCT and ongoing therapy; vaccination at least 6 months post-ASCT is common but earlier vaccination can still elicit response.
  • Monitor patients on active therapy closely as they have higher risk of vaccination failure.

Monitoring & Follow-up

  • Measure antibody titers approximately 4 weeks after completion of vaccination regimen.
  • Perform cellular immunity assays in seronegative patients to evaluate T-cell response.
  • Regular follow-up to detect post-vaccination COVID-19 cases.

Risks

  • Reduced vaccine immunogenicity in patients on active hematological malignancy therapy.
  • Potential for lower cellular immune response in seronegative patients.

Patient & Prescribing Data

64 adult patients with hematological malignancies post-ASCT receiving Comirnaty vaccine

High seroconversion rate (87%) overall; vaccination failure more frequent in patients on active therapy and those without ASCT as last treatment; antibody titers correlated positively with absolute lymphocyte count.

Clinical Best Practices

  • Administer mRNA SARS-CoV-2 vaccines to patients with hematological malignancies including post-ASCT patients.
  • Schedule vaccination considering timing of ASCT and current therapy status to optimize immune response.
  • Use both humoral and cellular immunity assays to comprehensively assess vaccine response, especially in seronegative patients.
  • Maintain vigilant follow-up for COVID-19 infection post-vaccination in this high-risk population.

References

Original Source(s)

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