The Immune Reaction Upon COVID-19 Vaccination in the Belgian Cancer Population.

University Hospital, Antwerp402 enrolled

Overview

This study investigates the immune response in the cancer population in Belgium being vaccinated with an approved vaccine types being authorized for use in Belgium. This question needs to be answered to make sure that this vulnerable population is properly protected against possible SARS-CoV-2 infection and that vaccine administration is safe.

Rationale: Patients with cancer have an increased risk of adverse outcome of COVID-19 and should be at high prioritisation for vaccination against SARS-CoV-2. The COVID-19 vaccine trials have not included cancer patients as such, the efficacy and duration of immunity in patients with cancer are still unknown. Keeping in mind that cancer patients are often immunocompromised, the immune response upon vaccination needs further investigation. The REAL-V is a prospective, multicenter cohort study. The humoral immunity response based on anti-SARS-CoV-2 IgG antibodies upon COVID-19 vaccination will be investigated in blood samples taken 4 months, 6 months and 12 months after (first) vaccine administration. Potential factors that affect immunity, will be recorded, such as type and stage of cancer, anti-cancer treatment, concomitant medication,..To investigate the safety of different COVID-19 vaccines, incidence and severity of systemic adverse events will be reported using an App based system answering questionnaires about specific vaccine related complaints.

Study Type

INTERVENTIONAL

Allocation

Purpose

PREVENTION

Masking

NONE

Enrollment

402

Conditions

Cancer

Interventions

Blood samplingOTHER

Blood sampling before and after COVID-19 vaccination

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Age of 18 years or older * Oncological or hematological malignancy or history of it * Life expectancy \> 3 months * Ability to provide informed consent Exclusion Criteria: * Women who are pregnant or breastfeeding * Immune deficiency not related to cancer or cancer treatment * Allergy (multiple); to be determined by physician

Locations (8)

University Hospital Antwerp

Edegem, Antwerp, Belgium

AZ Klina

Brasschaat, Belgium

AZ Sint Jan

Bruges, Belgium

UZ Brussel

Brussels, Belgium

Outcomes

Primary Outcomes

Immune response

The primary endpoint is the quantification of different anti-SARS-CoV-2 specific IgG antibodies 4 months after (first) vaccine administration. Antibody titers to the full Spike, S1, S2, RBD (receptor binding domain) and N (nucleocapsid) protein of SARS-CoV-2 will be measured quantitatively. For this measurement a multiplex SARS-CoV-2 immunoassay will be used.

Time frame: 4 months

Secondary Outcomes

Duration of the immune response

To study the evolution and duration of the immune response after vaccination: using serological assays to analyze anti-RBD IgG titers 6 months after (first) vaccine administration.

Time frame: 6 months

Neutralizing capacity

To analyze the titer of neutralizing antibodies both 4 and 6 months after (first) vaccine administration

Time frame: 6 months

Efficacy of the immune response

This will be assessed by the SARS-Cov2 infection rate based on information collected through questionnaires on incidence of (PCR-confirmed) SARSCoV-2 infection within a time-frame of 12 months after the start of the study.

Time frame: 12 months

Vaccine safety

Safety will be reported in terms of incidence and severity of systemic adverse events (AEs) during a continuous App based reporting system or using a questionnaire 3 days after vaccine administration.

Time frame: 12 months

Data from ClinicalTrials.gov

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