Tixagevimab/cilgavimab for Omicron SARS-CoV-2 infection in patients with haematologic diseases - Scorecard - MDSpire

Tixagevimab/cilgavimab for Omicron SARS-CoV-2 infection in patients with haematologic diseases

  • By

  • Armelle Otiniano

  • Zoe van de Wyngaert

  • Eolia Brissot

  • Rémy Dulery

  • Joel Gozlan

  • Anne Daguenel

  • Yasmine Abi Aad

  • Laure Ricard

  • Nicolas Stocker

  • Anne Banet

  • Agnes Bonnin

  • Tamim Alsuliman

  • Zora Marjanovic

  • Aurélie Schnuriger

  • Paul Coppo

  • Ollivier Legrand

  • Karine Lacombe

  • Mohamad Mohty

  • Florent Malard

  • December 8, 2022

  • 0 min

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Clinical Scorecard: Efficacy of Tixagevimab and Cilgavimab Against Omicron SARS-CoV-2 in Individuals with Hematologic Disorders

At a Glance

CategoryDetail
ConditionOmicron SARS-CoV-2 infection in patients with hematologic malignancies
Key MechanismsMonoclonal antibodies tixagevimab-cilgavimab target spike protein; partial neutralizing activity against Omicron variants
Target PopulationAdults and adolescents with hematologic malignancies, low anti-S IgG (<260 BAU/ml), at high risk of severe COVID-19
Care SettingHospitalized hematology department; compassionate use program

Key Highlights

  • Tixagevimab-cilgavimab shows ~12-fold decreased neutralizing activity against Omicron but retains partial efficacy.
  • In a retrospective study of 13 patients with hematologic malignancies and Omicron infection, asymptomatic patients treated early with tixagevimab-cilgavimab did not progress to severe COVID-19.
  • Symptomatic patients requiring oxygen had mixed outcomes; some recovered with tixagevimab-cilgavimab ± steroids, while others experienced prolonged disease or death.

Guideline-Based Recommendations

Diagnosis

  • Confirm Omicron SARS-CoV-2 infection by type-specific multiplex RT-PCR assay.
  • Assess anti-S IgG levels to identify weak or absent vaccine response (<260 BAU/ml).

Management

  • Administer intravenous tixagevimab-cilgavimab 300–300 mg for treatment in high-risk patients with low anti-S IgG.
  • Consider steroids (dexamethasone or prednisolone) and tocilizumab for inflammatory syndrome.
  • Early treatment in asymptomatic or mild cases may prevent progression to severe disease.

Monitoring & Follow-up

  • Monitor clinical symptoms and oxygen requirements closely.
  • Perform follow-up serological assessment to evaluate anti-S IgG increase post-treatment.
  • Watch for prolonged viral shedding and late respiratory deterioration.

Risks

  • Potential for treatment failure and progression to severe COVID-19 in symptomatic patients despite therapy.
  • High mortality risk remains in hospitalized patients with hematologic malignancies and Omicron infection.

Patient & Prescribing Data

Patients with hematologic malignancies infected with Omicron SARS-CoV-2, low anti-S IgG, including vaccinated and unvaccinated individuals.

Tixagevimab-cilgavimab increases anti-S IgG levels; early administration in asymptomatic patients prevents severe disease; symptomatic patients may require additional therapies.

Clinical Best Practices

  • Screen patients with hematologic malignancies for SARS-CoV-2 infection and antibody levels promptly.
  • Initiate tixagevimab-cilgavimab treatment early in asymptomatic or mild cases to prevent progression.
  • Use adjunctive steroids or immunomodulators in patients with inflammatory syndrome.
  • Monitor patients for delayed respiratory worsening and consider additional treatments such as convalescent plasma if needed.
  • Resume chemotherapy promptly in patients recovering from mild or asymptomatic COVID-19 after treatment.

References

Original Source(s)

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