Official Title
Immune Response to Third Dose of SARS-CoV-2 Vaccine in a Cohort of Cancer Patients on Active Treatment
Brief Summary

The Coronavirus Disease 2019 (COVID-19) pandemic has claimed over 5 million livesglobally. Fortunately, a substantial and growing number of SARS-CoV-2 vaccines with veryhigh efficacy have been developed, manufactured, and rapidly approved. Novel mRNAvaccines such as the BNT162b2 (Pfizer-BioNTech) and mRNA-1273 (Moderna) have reported astunning >94% efficacy against COVID-19. However, global access has not been equitable,with many low- and middle-income countries having no vaccine access or access underemergency use mainly to traditional inactivated SARS-CoV2-2 vaccines such as BBIBP-CorV(Sinopharm Beijing), CoronaVac (Sinovac) and BBV152 (Bharat Biotech). Emerging studieshave shown that lower concentrations of neutralizing antibodies (Nab) are attained afterCoronaVac than after a mRNA-based vaccine in healthy individuals. This difference seemsto be more pronounced in immunocompromised patients who are at higher risk of severeCOVID-19 and death from COVID-19. As such several countries including United States,Israel and Chile have recommended a third vaccine dose for this vulnerable population.In this observational study we will explore the humoral response to the BNT162b2 vaccinein patients who received two previous doses of the inactivated vaccine Coronavac or twodoses of BNT162b2.

Detailed Description

Not Provided

Unknown status
SARS-CoV-2 Infection

Biological: Three doses of BNT162b2 (observational)

BNT162b2 (COVID 19 mRNA vaccine)

Biological: Two doses of Coronavac and one dose BNT162b2 (observational)

BNT162b2 (COVID 19 mRNA vaccine) Coronavac (COVID 19 inactive vaccine)

Eligibility Criteria

Inclusion Criteria:

- Vaccination with two doses of Coronavac vaccine or BNT162b2 vaccine

- Eastern Cooperative Oncology group performance status < 3

Exclusion Criteria:

- Previous SARS-CoV-2 infection

- Vaccination with booster vaccine more than 12 weeks before informed consent

- Intravenous inmunoglobulin therapy 60 days before informed consent

- Any condition that could interfere with the paticipant´s participation during the
study in the opinion of the treating investigator.

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
Chile
Locations

Red de Salud UC Christus
Santiago, Chile

Investigator: Bruno Nervi
Contact: +56978073559
bnervi@gmail.com

Contacts

Bruno Nervi
9978073559
bnervi@gmail.com

Not Provided

Pontificia Universidad Catolica de Chile
NCT Number
MeSH Terms
COVID-19