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Completed

NCT Number: NCT05074706

Evaluation of the Immune Response to Sars-Covid-19 Vaccines in Haematological Patients: Prospective Single Center Study

The main objective of this study is to investigate the humoral immune response to COVID-19 vaccines in haematological patients, by testing SARS-CoV-2 seroconversion

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

San Gerardo Hospital

Monza, Lombardy, 20900, Italy

About this study

This single-center prospective study will enroll approximately 700 hematologic patients who access to Haematological Division (San Gerardo Hospital, Monza, Italy) in order to perform their routine blood tests to monitor their hematological conditions. Evaluation of Sars-Cov-2 IgG specific antibodies will be performed on left-over biological material (serum or plasma) collected during routine blood tests run between 30 and 60 days after the administration of the second vaccine dose.

Furthermore, in each patient who has failed seroconversion (absence of specific antibodies for circulation), his cellular immune response will be assessed using an additional blood sample collected during routine blood tests.

These samples will be collected within 9 months of the completion of the vaccination series and will be used to evaluate the plasma INF-γ release using QuantiFERON SARS-CoV-2 test.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed and dated EC-approved informed consent
  • Hematological disease defined according to World Health Organization (WHO) criteria
  • Female or male, 18 years of age or older
  • ECOG performance status 0-3
  • Willingness and ability to comply with routine clinical practice and study procedures
  • Regular vaccination against SARS-CoV-2 according to Italian Haematological Society (SIE) guidelines/recommendations (Version 2.0, 20 April, 2021).
  • Routine blood test planned between 30 and 60 days after administration of the second vaccine dose according to regular hematological follow up.
  • Routine blood test planned no later than 9 months after the completion of the vaccination series (only in case of absence of circulation specific antibodies).

Exclusion criteria

  • Preventive vaccination against SARS-CoV-2 not administered according to Italian Haematological Society (SIE) guidelines/recommendations (Version 2.0, 20 April, 2021)
  • Evidence of previous infection with the SARS-Cov-2 virus.
  • Routine blood test not planned between 30 and 60 days after administration of the second vaccine dose.
  • Routine blood test not planned within 9 months after the completion of the vaccination series (only in case of absence of circulation specific antibodies).

Treatment and study plan

IgG antibodies to Sars-Cov-2

Biological

Samples will be collected between 30 and 60 days after second vaccine dose.

Other names: Blood serum SARS-CoV-2 IgG

QuantiFERON SARS-CoV-2 test

Biological

Samples will be collected within 9 months after completion of the vaccination series

Other names: Plasma INF-γ

Primary outcomes

  1. Rate of seroconversion in hematological patients who received a mRNA SARS-CoV-2 vaccine

    Time frame: Between 30 and 60 days after the administration of the second vaccine dose

    Seroconversion is defined as a post-vaccination SARS-CoV-2 IgG antibody titer >33.8 Binding Anticorpal Unit (BAU)/ml.

Secondary outcomes

  1. To compare the seroconversion rate in haematological patients versus healthy subjects.

    Time frame: Between 30 and 60 days after the administration of the second vaccine dose

    Time adjusted rate of seroconversion after vaccination in hematological patient and healthy population.

  2. To correlate the rate of seroconversion in hematological patients to the specific haematological diseases.

    Time frame: Between 30 and 60 days after the administration of the second vaccine dose

    Rate of seroconversion per type of haematological condition

  3. To correlate the rate of seroconversion to previous therapies

    Time frame: Between 30 and 60 days after the administration of the second vaccine dose

    Rate of seroconversion per specific treatment.

  4. To assess the efficacy of vaccine by estimating how many patients will be infected by SARS-CoV-2 in the 9 months after the administration of the second vaccine dose.

    Time frame: Within 9 months after the administration of the second vaccine dose

    Rate of patients with a positive RT-PCR-SARS-CoV-2 test in the 9 months after the administration of the second vaccine dose

  5. To analize T-cell response in those patients who will result negative for specific antibodies anti-Sars-Cov-2 after two doses of mRNA SARS-Cov-2 vaccination

    Time frame: Within 9 months after the administration of the second vaccine dose

    Rate of patients with a positive QuantiFERON-SARS-CoV-2 test after the demonstration of seroconversion failure until the end of the study

Sponsors and collaborators

Lead sponsor

University of Milano Bicocca

Other

Collaborators

  • San Gerardo Hospital

Registry information

Official study title

Evaluation of the Immune Response to Sars-Covid-19 (Cov-2) Vaccines in Haematological Patients: Prospective Single Center Study

Acronym: Hema-C19-Vax

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Oct 12, 2021
Registry last updated
Jan 25, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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